Patent Grant
10071089
The present invention relates to an oral pharmaceutical dosage form comprising oxycodone or a pharmaceutically acceptable salt thereof and naloxone or a pharmaceutically acceptable salt thereof for use in the treatment of pain in patients suffering from i) pain and at least one further disease ii) resulting in intestinal dysbiosis and/or at least one further disease iii) increasing the risk for intestinal bacterial translocation resulting inter alia in peritonitis.
It has been established over the last years that a number of diseases inter alia affect the intestinal microbiota. An example in this respect is colorectal cancer (Zhu et al., “Gut microbiota and probiotics in colon tumorigeneses”, Cancer Letters, 2011, Vol. 309, pages 119-127). Further, it is known that a number of diseases increase the susceptibility for bacterial translocation resulting inter alia in peritonitis, (such as e.g. cirrhosis) or in systemic inflammatory response syndrome (SIRS) or sepsis (such as e.g. pancreatitis, cholangitis, burn injury or trauma) (Gatt et a., “Review article: bacterial translocation in the critically ill—evidence and methods of prevention”, Aliment Pharmacol Ther 25, pages 741-757).
It has further been established that the intestinal microbiota plays an important role in several essential processes in the human body; thus, the microbiota inter alia performs a protective function, a metabolic function and a structural function. An impaired intestinal microbiota may thus result in changes in the metabolic profile, impairment of GI transit and pathogen overgrowth. Treatment regimens for diseases affecting the intestinal microbiota may include the administration of probiotics in order to restore or at least improve the impaired intestinal microbiota.
Patients suffering from a disease resulting in an impaired microbiota or increasing the susceptibility for intestinal bacterial translocation may not only suffer from the underlying disease but also from pain due to various reasons. Thus, a patient suffering from colorectal cancer may also suffer from severe back pain, wherein said back pain may have a completely different origin. The back pain may be that severe that the patient requires a long term analgesic therapy.
Opioids correspond to the most efficient analgesics if moderate to severe pain requires treatment. However, several side effect of opioid therapy are known; one of the most prominent side effects is opioid-induced constipation, which is also affecting the GI-tract.
If one were to treat the above mentioned patient suffering from colorectal cancer and back pain with an opioid, it can be expected that the impaired microbiota will likely not improve but, to the contrary, rather worsen. The same is true for a patient suffering from pain and a disease, which increases the risk for intestinal bacterial translocation; the use of an opioid in such a patient will even further increase the susceptibility to intestinal bacterial translocation. Further, patients suffering from pancreatitis, cholangitis, burn injury or trauma may be more susceptible to bacterial translocation resulting in systemic inflammatory response syndrome (SIRS) or sepsis; the use of an opioid in such patients will even further increase the susceptibility to systemic inflammatory response syndrome (SIRS) or sepsis. As a consequence, opioids may not be used for pain treatment in such patients, resulting in the undertreatment of pain.
It is evident from the above that there is a need for a pharmaceutical composition, which is capable of treating pain in a patient suffering from pain and a further disease, which is negatively affecting the intestinal microbiota and/or increasing the susceptibility for intestinal bacterial translocation (resulting inter alia in peritonitis), wherein the pharmaceutical composition fails to have a negative impact on the intestinal microbiota and may even improve the intestinal microbiota and/or decrease the risk for intestinal bacterial translocation.
The inventors of the present invention surprisingly found that a pharmaceutical dosage form comprising the active agents oxycodone and naloxone is suitable for treating pain in a specific patient population, namely patients suffering from pain and a further disease, which results in intestinal dysbiosis (i.e. a further disease, which is negatively affecting the intestinal microbiota) and/or a further disease, which increases the risk for intestinal bacterial translocation (potentially leading to SIRS, sepsis and/or peritonitis).
In a first object, the present invention is thus directed to a pharmaceutical dosage form for use in the treatment of pain in patients suffering from pain and at least one further disease resulting in intestinal dysbiosis and/or a further disease, which increases the risk for peritonitis.
In a second object, the present invention is concerned with methods of treating pain in a subject suffering from pain and at least one further disease resulting in intestinal dysbiosis and/or a further disease increasing the risk for peritonitis.
Thus, in the most preferred embodiment, the present invention relates to an oral pharmaceutical dosage form comprising oxycodone or a pharmaceutically acceptable salt thereof and naloxone or a pharmaceutically acceptable salt thereof for use in the treatment of pain in patients suffering from i) pain and at least one further disease ii) selected from the group consisting of colorectal cancer, inflammatory bowel disease including Crohn's disease and ulcerative colitis, obesity, autism, irritable bowel syndrome, metabolic syndrome, rheumatoid arthritis, allergy, diabetes mellitus including type 2 diabetes, sepsis, Parkinson's disease, autonomic neuropathy including autonomic neuropathy in type 2 diabetes, scleroderma, achlorhydria, pancreatic exocrine insufficiency, immune-deficiency syndromes, small intestinal obstruction, diverticulitis, fistulae, surgical blind loop, previous ileo-caecal resections, post-radiation enteropathy, small intestinal pseudo-obstruction, small intestinal bacterial overgrowth syndrome, vaginal mycosis, intestinal mycosis, multiple system atrophy, food intolerance, intestinal infections, gallstones and hyperactivity of the immune system, wherein said at least one further disease ii) results in intestinal dysbiosis, and/or at least one further disease iii) selected from the group consisting of cirrhosis, hepatitis, appendicitis, pancreatitis, chronic kidney disease and cholecystitis, wherein said at least one further disease iii) increases the risk for peritonitis.
The wording used above is to be understood in the following meaning, which is to be applied throughout the present specification: an oral pharmaceutical dosage form comprising oxycodone or a pharmaceutically acceptable salt thereof and naloxone or a pharmaceutically acceptable salt thereof for use in the treatment of pain in patients suffering from i) pain and at least one further disease ii) selected from the group consisting of colorectal cancer, inflammatory bowel disease including Crohn's disease and ulcerative colitis, obesity, autism, irritable bowel syndrome, metabolic syndrome, rheumatoid arthritis, allergy, diabetes mellitus including type 2 diabetes, sepsis, Parkinson's disease, autonomic neuropathy including autonomic neuropathy in type 2 diabetes, scleroderma, achlorhydria, pancreatic exocrine insufficiency, immune-deficiency syndromes, small intestinal obstruction, diverticulitis, fistulae, surgical blind loop, previous ileo-caecal resections, post-radiation enteropathy, small intestinal pseudo-obstruction, small intestinal bacterial overgrowth syndrome, vaginal mycosis, intestinal mycosis, multiple system atrophy, food intolerance, intestinal infections, gallstones and hyperactivity of the immune system, wherein said at least one further disease ii) results in intestinal dysbiosis, and/or for use in the treatment of pain in patients suffering from i) pain and at least one further disease iii) selected from the group consisting of cirrhosis, hepatitis, appendicitis, pancreatitis, chronic kidney disease and cholecystitis, wherein said at least one further disease iii) increases the risk for peritonitis.
Thus, there is no link at all between disease ii) and disease iii); rather, a patient may suffer from
In other words, the presence of disease iii) is not an inevitable result of having disease ii).
In a preferred embodiment, the present invention relates to an oral pharmaceutical dosage form comprising oxycodone or a pharmaceutically acceptable salt thereof and naloxone or a pharmaceutically acceptable salt thereof for use in the treatment of pain in patients suffering from i) pain and at least one further disease ii) selected from the group consisting of colorectal cancer, inflammatory bowel disease including Crohn's disease and ulcerative colitis, obesity, autism, irritable bowel syndrome, metabolic syndrome, rheumatoid arthritis, allergy, diabetes mellitus including type 2 diabetes, sepsis, Parkinson's disease, autonomic neuropathy including autonomic neuropathy in type 2 diabetes, scleroderma, achlorhydria, pancreatic exocrine insufficiency, immune-deficiency syndromes, small intestinal obstruction, diverticulitis, fistulae, surgical blind loop, previous ileo-caecal resections, post-radiation enteropathy, small intestinal pseudo-obstruction, small intestinal bacterial overgrowth syndrome, vaginal mycosis, intestinal mycosis, multiple system atrophy, food intolerance, intestinal infections, gallstones and hyperactivity of the immune system, wherein said at least one further disease ii) results in intestinal dysbiosis.
In another preferred embodiment, said at least one further disease ii) is selected from the group consisting of colorectal cancer, obesity, autism, irritable bowel syndrome, metabolic syndrome, rheumatoid arthritis, allergy, type 2 diabetes, sepsis, autonomic neuropathy in type 2 diabetes, scleroderma, achlorhydria, pancreatic exocrine insufficiency, immune-deficiency syndromes, small intestinal obstruction, diverticulitis, fistulae, surgical blind loop, previous ileo-caecal resections, post-radiation enteropathy, small intestinal pseudo-obstruction, small intestinal bacterial overgrowth syndrome, vaginal mycosis, intestinal mycosis, multiple system atrophy, food intolerance, intestinal infections, gallstones and hyperactivity of the immune system.
In another preferred embodiment, said at least one further disease ii) is selected from the group consisting of colorectal cancer, obesity, autism, irritable bowel syndrome, metabolic syndrome, rheumatoid arthritis, allergy, type 2 diabetes, sepsis, autonomic neuropathy in type 2 diabetes, scleroderma, achlorhydria, pancreatic exocrine insufficiency, small intestinal obstruction, diverticulitis, fistulae, previous ileo-caecal resections, post-radiation enteropathy, small intestinal pseudo-obstruction and small intestinal bacterial overgrowth syndrome.
In yet another preferred embodiment, said at least one further disease ii) is selected from the group consisting of colorectal cancer, obesity, autism, irritable bowel syndrome, metabolic syndrome, sepsis and small intestinal bacterial overgrowth syndrome.
In a particularly preferred embodiment, said patient is suffering from i) pain and ii) diverticulitis. In another particularly preferred embodiment, said patient is suffering from i) pain and ii) small intestinal bacterial overgrowth syndrome. In yet another particularly preferred embodiment, said patient is suffering from i) pain and ii) ulcerative colitis. In another particularly preferred embodiment, said patient is suffering from i) pain and ii) colorectal cancer.
In yet another preferred embodiment, the present invention relates to an oral pharmaceutical dosage form comprising oxycodone or a pharmaceutically acceptable salt thereof and naloxone or a pharmaceutically acceptable salt thereof for use in the treatment of pain in patients suffering from i) pain and at least one further disease iii) selected from the group consisting of cirrhosis, pancreatitis, chronic kidney disease and cholecystitis, wherein said at least one further disease iii) increases the risk for peritonitis.
In yet another preferred embodiment, the present invention relates to an oral pharmaceutical dosage form comprising oxycodone or a pharmaceutically acceptable salt thereof and naloxone or a pharmaceutically acceptable salt thereof for use in the treatment of pain in patients suffering from i) pain and at least one further disease iii) increasing the risk for peritonitis, wherein said at least one further disease iii) is selected from the group consisting of cirrhosis, chronic kidney disease and cholecystitis. In a particularly preferred embodiment, said at least one further disease is cirrhosis.
The present invention is in particular directed in the first object to an oral pharmaceutical dosage form comprising oxycodone or a pharmaceutically acceptable salt thereof and naloxone or a pharmaceutically acceptable salt thereof for use in the treatment of pain in patients suffering from i) pain and at least one further disease ii), wherein said at least one further disease ii) results in intestinal dysbiosis, or for use in the treatment of pain in patients suffering from i) pain and at least one further disease iii), wherein said at least one further disease iii) increases the risk for intestinal bacterial translocation. One may also refer to said at least one further disease iii) as increasing the risk for intestinal bacterial translocation resulting in bacteriaemia and leading to sepsis, systemic inflammatory response syndrome (SIRS) and/or peritonitis. Alternatively, one may also refer to said at least one further disease iii) as increasing the risk for intestinal bacterial translocation, wherein said bacterial translocation would then result in peritonitis, systemic inflammatory response syndrome (SIRS) and/or sepsis. In consequence, one may also refer to said at least one further disease iii) as increasing the risk for peritonitis, systemic inflammatory response syndrome (SIRS) and/or sepsis. Said at least one further disease iii), which may also be designated as disease underlying or causing the increased risk for bacterial translocation (and thus for peritonitis, systemic inflammatory response syndrome (SIRS) and/or sepsis), is preferably selected from the group consisting of trauma, burn injury, pancreatitis and cholangitis.
Specific diseases ii) resulting in intestinal dysbiosis and specific diseases iii) increasing the risk for intestinal bacterial translocation are stated below and particularly in the dependent claims of the present application.
In a preferred embodiment, the present invention relates to an oral pharmaceutical dosage form comprising oxycodone or a pharmaceutically acceptable salt thereof and naloxone or a pharmaceutically acceptable salt thereof for use in the treatment of pain in patients suffering from i) pain and at least one further disease ii) selected from the group consisting of diseases linked to the stomach, small intestine, colon, colon and the small intestine, and diseases generally linked to the GI tract, wherein said at least one further disease ii) results in intestinal dysbiosis. The treatment of patients suffering from i) pain and at least one further disease ii) selected from the group consisting of diseases linked to the stomach, small intestine, colon and the small intestine, and diseases generally linked to the GI tract, wherein said at least one further disease ii) results in intestinal dysbiosis, can be preferred. Further, the treatment of patients suffering from i) pain and at least one further disease ii) selected from the group consisting of diseases linked to the stomach, small intestine, and colon and small intestine, wherein said at least one further disease ii) results in intestinal dysbiosis, is preferred. Particularly preferred is the treatment of patients suffering from i) pain and at least one further disease ii) selected from the group consisting of diseases linked to the stomach, and small intestine, wherein said at least one further disease ii) results in intestinal dysbiosis.
In a particularly preferred embodiment, i) pain is not a symptom of the at least one further disease ii) and/or the at least one further disease iii) (i.e. at least one disease selected from the groups as defined above). In this embodiment, the pain is not caused by the at least one further disease ii) or the at least one further disease iii). In other words, the pain is unrelated to the at least one further disease ii) or the at least one further disease iii) and has a different origin.
In other words, another embodiment of the present invention relates to an oral pharmaceutical dosage form comprising oxycodone or a pharmaceutically acceptable salt thereof and naloxone or a pharmaceutically acceptable salt thereof for use in the treatment of pain in patients which otherwise have to totally abstain from opioid-based pain therapy due to the presence of not opioid-induced intestinal dysbiosis as a result of at least one further disease ii) as defined above. Moreover, another embodiment of the present invention relates to an oral pharmaceutical dosage form comprising oxycodone or a pharmaceutically acceptable salt thereof and naloxone or a pharmaceutically acceptable salt thereof for use in the treatment of pain in patients which otherwise have to totally abstain from opioid-based pain therapy since said patients are already at increased risk for intestinal bacterial translocation (resulting inter alia in peritonitis, SIRS and/or sepsis), i.e. particularly susceptible for intestinal bacterial translocation (including susceptibility for peritonitis, SIRS and/or sepsis), as a results of at least one further disease iii) as defined above.
In another preferred embodiment, said intestinal dysbiosis is not induced by an opioid agonist but by said at least one further disease ii); one may also refer to said intestinal dysbiosis as being initially (i.e. prior to the treatment) not induced by an opioid agonist but by said at least one further disease ii).
In another preferred embodiment, said increased risk for intestinal bacterial translocation is not induced by an opioid agonist but by said at least one further disease iii); one may also refer to said increased risk for intestinal bacterial translocation as being initially (i.e. prior to the treatment) not induced by an opioid agonist but by said at least one further disease iii).
Thus, one may also refer to the above patients suffering from i) pain and the at least one further disease ii) and/or the at least one further disease iii) as defined above as opioid-naïve patients.
In a further preferred embodiment, said pain is moderate to severe pain.
In another preferred embodiment, oxycodone or a pharmaceutically acceptable salt thereof and naloxone or a pharmaceutically acceptable salt thereof are the only pharmaceutically active agents comprised in said dosage form.
Further, a co-administration of an active agent directed to the improvement of the intestinal dysbiosis (such as e.g. probiotics) and/or of an active agent directed to the improvement of opioid-induced constipation and/or opioid-induced bowel dysfunction (such as e.g. a laxative) may not be necessary. Thus, the pain treatment regimen in a patient population suffering from i) pain and a disease ii) resulting in intestinal dysbiosis as defined above may exclude the co-administration of an active agent directed to the improvement of the intestinal dysbiosis and/or of an active agent directed to the improvement of opioid-induced constipation and/or opioid-induced bowel dysfunction.
Also, a co-administration of an active agent decreasing the risk for intestinal bacterial translocation (such as e.g. antibiotics) and/or of an active agent directed to the improvement of opioid-induced constipation and/or opioid-induced bowel dysfunction (such as e.g. a laxative) may not be necessary. Thus, the pain treatment regimen in a patient population suffering from i) pain and a disease iii) increasing the risk for intestinal bacterial translocation as defined above may exclude the co-administration of an active agent directed at lowering the risk for intestinal bacterial translocation and/or of an active agent directed to the improvement of opioid-induced constipation and/or opioid-induced bowel dysfunction.
In another preferred embodiment, the dosage form comprises oxycodone or a pharmaceutically acceptable salt thereof in an amount range of equivalent to about 1 mg to about 160 mg oxycodone HCl and naloxone or a pharmaceutically acceptable salt thereof in an amount range of equivalent to about 0.5 mg to about 80 mg naloxone HCl.
The dosage form may preferably comprise oxycodone or a pharmaceutically acceptable salt thereof in an amount of equivalent to about 2.5 mg, to about 5 mg, to about 10 mg, to about 15 mg, to about 20 mg, to about 40 mg, to about 50 mg, to about 60 mg, to about 80 mg, to about 100 mg, to about 120 mg, to about 140 mg, or to about 160 mg oxycodone HCl. Naloxone or a pharmaceutically acceptable salt thereof may be present in an amount of equivalent to about 0.5 mg, to about 1 mg, to about 1.5 mg, to about 2 mg, to about 4 mg, to about 5 mg, to about 10 mg, to about 15 mg, to about 20 mg, to about 40 mg, to about 60 mg, or to about 80 mg naloxone HCl.
In yet another preferred embodiment, the dosage form comprises oxycodone or a pharmaceutically acceptable salt thereof and naloxone or a pharmaceutically acceptable salt thereof in a weight ratio range of from about 6:1 to about 1:1 (oxycodone:naloxone).
In another preferred embodiment, the dosage form comprises oxycodone or a pharmaceutically acceptable salt thereof and naloxone or a pharmaceutically acceptable salt thereof in a 2:1 ratio by weight.
Thus, preferred embodiments relate to dosage forms comprising amounts of equivalent to about 2.5 mg oxycodone HCl and about 1.25 mg naloxone HCl; about 5 mg oxycodone HCl and about 2.5 mg naloxone HCl; about 10 mg oxycodone HCl and about 5 mg naloxone HCl; about 20 mg oxycodone HCl and about 10 mg naloxone HCl; about 40 mg oxycodone HCl and about 20 mg naloxone HCl; about 80 mg oxycodone HCl and 40 mg naloxone HCl; and about 160 mg oxycodone HCl and about 80 mg naloxone HCl.
In another preferred embodiment, the pharmaceutically acceptable salt of the opioid agonist and/or the opioid antagonist is selected from the group comprising the hydrochloride, sulphate, bisulphate, tartrate, nitrate, citrate, bitartrate, phosphate, malate, maleate, hydrobromide, hydroiodide, fumerate and succinate salt. It can be particularly preferred that the salt is the hydrochloride salt.
Furthermore, in an also preferred embodiment, the dosage form may comprise further pharmaceutically acceptable ingredients and/or adjuvants, such as e.g. lubricants, fillers, binders, flowing agents, colorants, flavorants, surfactants, pH-adjusters, anti-tacking agents and/or combinations thereof.
In another preferred embodiment, the dosage form is a prolonged release dosage form.
It can be preferred that the prolonged release dosage form comprises a prolonged release matrix. It can further be preferred that said matrix comprises a fatty alcohol and/or a hydrophobic polymer, preferably an alkylcellulose and more preferably ethylcellulose.
It can also be preferred that the prolonged release dosage form comprises a prolonged release coating.
In a further preferred embodiment, the prolonged release dosage form is an osmotic prolonged release dosage form.
Further, the dosage form according to the present invention may also be an immediate release dosage form.
Preferably, the dosage form according to the present invention is a dosage form selected from the group consisting of a tablet, a capsule, a multi-particulate, a dragée, a granulate and a powder. A particularly preferred dosage form is a tablet or a multi-particulate. Since both active agents, i.e. oxycodone and naloxone, are comprised in a single dosage form, said two active agents are not administered sequentially.
In a second object, the present invention is concerned with a method of treating pain comprising administering an oral pharmaceutical dosage form comprising oxycodone or a pharmaceutically acceptable salt thereof and naloxone or a pharmaceutically acceptable salt thereof to a patient suffering from i) pain and at least one further disease ii) selected from the group consisting of colorectal cancer, inflammatory bowel disease including Crohn's disease and ulcerative colitis, obesity, autism, irritable bowel syndrome, metabolic syndrome, rheumatoid arthritis, allergy, diabetes including type 2 diabetes, sepsis, Parkinson's disease, autonomic neuropathy including autonomic neuropathy in type 2 diabetes, scleroderma, achlorhydria, pancreatic exocrine insufficiency, immune-deficiency syndromes, small intestinal obstruction, diverticulitis, fistulae, surgical blind loop, previous ileo-caecal resections, post-radiation enteropathy, small intestinal pseudo-obstruction, small intestinal bacterial overgrowth syndrome, vaginal mycosis, intestinal mycosis, multiple system atrophy, food intolerance, intestinal infections, gallstones and hyperactivity of the immune system, wherein said at least one further disease ii) results in intestinal dysbiosis, and/or at least one further disease iii) selected from the group consisting of cirrhosis, hepatitis, appendicitis, pancreatitis, chronic kidney disease and cholecystitis, wherein said at least one further disease iii) increases the risk for peritonitis.
In the second object, the present invention is also concerned with a method of treating pain comprising administering an oral pharmaceutical dosage form comprising oxycodone or a pharmaceutically acceptable salt thereof and naloxone or a pharmaceutically acceptable salt thereof to a patient suffering from i) pain and at least one further disease ii), wherein said at least one further disease ii) results in intestinal dysbiosis, or a method of treating pain comprising administering said oral pharmaceutical dosage form to a patient suffering from i) pain and at least one further disease iii), wherein said at least one further disease iii) increases the risk for intestinal bacterial translocation.
All embodiments mentioned above for the first object also apply for the second object of the present invention.
The inventors of the present invention inter alia succeeded in providing a pharmaceutical dosage form for use in the treatment of pain in patients suffering from i) pain and at least one further disease ii), e.g. as defined herein, resulting in intestinal dysbiosis. Further, the inventors were successful in providing a pharmaceutical dosage form, which can be used for pain treatment in patients suffering from i) pain and are particularly susceptible for intestinal bacterial translocation (and thus e.g. peritonitis, SIRS and/or sepsis), e.g. due to at least one further disease iii) as defined herein.
Before some of the embodiments of the present invention are described in more detail, the following definitions are introduced.
Definitions
As used in the specification and the claims, the singular forms of “a” and “an” also include the corresponding plurals unless the context clearly dictates otherwise.
The term “about” in the context of the present invention denotes an interval of accuracy that a person skilled in the art will understand to still ensure the technical effect of the feature in question. The term typically indicates a deviation from the indicated numerical value of ±10% and preferably ±5%.
It needs to be understood that the term “comprising” is not limiting. For the purposes of the present invention, the term “consisting of” is considered to be a preferred embodiment of the term “comprising”. If hereinafter a group is defined to comprise at least a certain number of embodiments, this is also meant to encompass a group which preferably consists of these embodiments only.
“Treatment of pain” is to be understood as referring to a general improvement or even cure of the patient's pain or to the alleviation of pain. Such an improvement/cure or alleviation can either be detected by the patient's subjective feeling or by external observations. The intensity of pain may e.g. be assessed using a pain intensity scale; this scale may refer to the average pain over the last 24 hours (Scale of 0-10, 0=no pain; 10=strong pain).
The term “microbiota” is interchangeably used herein with the terms “microbiome” and “(micro)flora” and refers to the totality of microbial cells in the human body, wherein the present invention has a particular focus on the totality of microbial cells in the GI tract or gut. The GI tract is inhabited with 1013 to 1014 microorganisms (thought to be 10 times that of the number of human cells in the body and 100 times as many genes as the human genome). The estimated species number varies greatly but it is generally accepted that the adult microbiota consists of greater than 1000 species and more than 700 strains. It is an environment dominated by bacteria, mainly strict anaerobes, but also including viruses, protozoa, archaea and fungi (see introductory part of Grenham et al., “Brain-gut-microbe communication in health and disease”, Frontiers in physiology, 2011, Vol. 2, Article 94, for further details).
The term “intestinal dysbiosis” means an impaired or altered intestinal microbiota. It may also be described as a shift in the makeup of the commensal microflora to a nonphysiologic composition. This may e.g. mean that obligate bacteria, Bifidobacteria, Lactobacilli and E. coli (apathogenic) are reduced relative to the normal intestinal microflora, wherein obligate bacteria may partly disappear and Bifidobacteria are reduced or almost disappear. Aerobes and Bacterioids, Clostridia, Streptococci, P. aeruginosa and other pathogenic bacteria, fungi, mould, lactose-negative enterobacteria and E. coli (pathogenic) may be increased relative to the normal intestinal microflora. In Wikipedia, the term “dysbiosis” is defined as follows: “Dysbiosis (also called “dysbacteriosis”) refers to microbial imbalance on or inside the body. Dysbiosis is most commonly reported as a condition in the digestive tract. It has been associated with illnesses, such as inflammatory bowel disease, chronic fatigue syndrome, obesity, cancer and colitis. Microbial colonies found on or in the body are normally benign or beneficial. These beneficial and appropriately sized microbial colonies carry out a series of helpful and necessary functions, such as aiding in digestion. They also protect the body from the penetration of pathogenic microbes. These beneficial microbial colonies compete with each other for space and resources and outnumber human cells by a factor 10:1. The term “dysbiosis” is not a standardized medical term. Apparently similar concepts are also described as “microbial imbalance”, “bacterial imbalance”, or “increased levels of harmful bacteria and reduced levels of the beneficial bacteria”.”
“Peritonitis” is used herein in its general meaning, i.e. as corresponding to an inflammation of the peritoneum. “Systemic inflammatory response syndrome (SIRS)” and “sepsis” are used herein in the general meaning, i.e. that SIRS is a clinical syndrome that complicates a noninfectious insult (e.g., acute pancreatitis, pulmonary contusion) and sepsis a clinical syndrome that complicates severe infection, respectively. The patient population suffering from at least one disease as listed herein under disease iii) is particularly vulnerable to developing peritonitis,
SIRS and/or sepsis. This means that the patient is not actually suffering from peritonitis, SIRS and/or sepsis but at a higher risk of developing peritonitis, SIRS and/or sepsis than a patient not suffering from at least one of the disease as listed herein under disease iii). The term “risk” and “susceptibility” are used interchangeably herein; “increased risk” or “increased susceptibility” means that patients are prone to a specific disease. The term “increases the risk for peritonitis” may also be understood as “results in a pre-condition of peritonitis” or as “makes the patient susceptible for peritonitis”. The term “increases the risk for systemic inflammatory response syndrome (SIRS)” or “sepsis” may also be understood as “results in a pre-condition of SIRS or sepsis” or as “makes the patient susceptible for SIRS or sepsis”.
The term “intestinal bacterial translocation” as used herein means that live bacteria and/or its products cross the intestinal barrier. Such a translocation will in almost all cases result in infectious complications. As noted above, specific diseases resulting from an intestinal bacterial translocation are peritonitis, SIRS and sepsis. Thus, the term “increases the risk for intestinal bacterial translocation” may also be understood as “results in a pre-condition of peritonitis, SIRS and/or sepsis” or “makes the patient susceptible for peritonitis, SIRS and/or sepsis”.
The term “opioid-naïve patient” means that the patient has not recently taken an opioid on a regular basis.
The term “probiotics” refers to live microorganisms, which, when administered in adequate amounts, confer a health benefit on the host.
“Hyperactivity of the immune system” as used herein comprises one or more of the following: increase of CD3+, CD4+, CD8+ T-cells and activated CD25+, spontaneous proliferation of lymphocytes and increased titer of certain anti-bacterial antibodies, e.g. E. coli and S. aureus antibodies, increased values of IgA and IgM to gram negative enterobacteria or their endotoxins such as Hafnia alvei, Pseudomonas aeruginosa, Morganella morganii, Proteus mirabilis, Pseudomonas putida, Citrobacter koseri and/or Klebsiella pneumoniae.
In the context of the present invention, the term “prolonged release” refers to pharmaceutical dosage forms showing a slower release of the active agents than that of a conventional release pharmaceutical dosage forms administered by the same route. Prolonged release is achieved by a special formulation design and/or manufacturing method. In general, “prolonged release dosage forms” in the context of the present invention means that oxycodone and naloxone are released from the pharmaceutical dosage form over an extended period of time.
The term “immediate release” as used herein refers to pharmaceutical dosage forms showing a release of the active substances which is not deliberately modified by a special formulation design and/or manufacturing methods.
“Pharmaceutically acceptable salts” include, but are not limited to, inorganic acid salts such as hydrochloride, hydrobromide, hydroiodide, sulfate, bisulfate, phosphate and the like; organic acid salts such as formate, acetate, trifluoroacetate, malate, maleate, tartrate, bitartrate, fumerate, succinate, citrate and the like; sulfonates such as methanesulfonate, benzenesulfonate, p-toluenesulfonate, and the like; amino acid salts such as arginate, asparginate, glutamate and the like, and metal salts such as sodium salt, potassium salt, cesium salt and the like; alkaline earth metals such as calcium salt, magnesium salt and the like; organic amine salts such as triethylamine salt, pyridine salt, picoline salt, ethanolamine salt, triethanolamine salt, dicyclohexylamine salt, N,N′-dibenzylethylenediamine salt and the like.
Detailed Description of the Patient Population and the Oral Dosage Form
The oral pharmaceutical dosage form according to the present invention is intended for treatment of pain in a patient population suffering from i) pain and ii) at least one further disease resulting in intestinal dysbiosis and/or iii) at least one further disease increasing the risk for intestinal bacterial translocation.
A link to intestinal dysbiosis has been established for the following diseases: colorectal cancer (see e.g. Azcarate-Peril et al., “The intestinal microbiota, gastrointestinal environment and colorectal cancer: a putative role for probiotics in prevention of colorectal cancer?”, Am J Physiol Gastrointest Liver Physiol, 2011, Vol. 301, No. 3, G401-24; Zhu et al., “Gut microbiota and probiotics in colon tumorigeneses”, Cancer Letters, 2011, Vol. 309, pages 119-127), inflammatory bowel disease including Crohn's disease and ulcerative colitis (see e.g. Salzmann and Bevins “Negative interactions with the microbiota: IBD”, Adv Exp Med Biol, 2008, Vol. 635, pages 67-78; Rausch et al., “Colonic mucosa-associated microbiota is influenced by an interaction of Crohn's disease and FUT2 (Secretor) genotype”, 2011, Vol. 108, No. 47, pages 19030-5), obesity (see e.g. Ley et al., “Obesity alters gut microbial ecology”, PNAS, 2005, Vol. 102, No. 31, pages 11070-11075), autism (see e.g. Grenham et al., “Brain-gut-microbe communication in health and disease”, Frontiers in physiology, 2011, Vol. 2, Article 94), irritable bowel syndrome (see e.g. O Noor et al., “Ulcerative colitis and irritable bowel patients exhibit distinct abnormalities of the gut and microbiota”, Gastroenterology, 2010, Vol. 10, No. 134; Ponnusamy et al., “Microbial Community and metabolomic comparison of irritable bowel syndrome faeces”, Journ Med Microbiol, 2011, Vol. 60, pages 817-827), metabolic syndrome (see e.g. Zhu et al., “Gut microbiota and probiotics in colon tumorigeneses”, Cancer Letters, 2011, Vol. 309, pages 119-127), rheumatoid arthritis (see e.g. Scher and Abramson, “The microbiome and rheumatoid arthritis”, Nat Rev Rheumatol., 2011, Vol. 7, No. 10, Pages 569-578), allergy (see e.g. Shreiner et al., “The ‘microflora hypothesis’ of allergic disease”, Adv Exp Med Bio, 2008, Vol. 635, pages 113-134), diabetes including type 2 diabetes (see e.g. Larsen et al., “Gut microbiota in human adults with type 2 diabetes differs from non-diabetic adults” PLOS ONE, 2010 (February), Vol. 5, No. 2), sepsis (see e.g. Harari et al., “The effect of morphine on mast cell-mediated mucosal permeability”, 2006, Surgery, Vol. 139, No. 1, pages 54-60; Runkel et al., “Alterations in rat intestinal transit by morphine promote bacterial translocation”, Dig Diseases and Sciences, 1993, Vol. 38, No. 8, pages 1530-1536), Parkinson's disease (see e.g. Jost, “Gastrointestinal dysfunction in Parkinson's disease”, J Neurol Scie, 2010, Vol. 289, No. 1-2, pages 69-73), scleroderma, achlorhydria, pancreatic exocrine insufficiency, immune-deficiency syndromes, small intestinal obstruction, diverticulitis, fistulae, surgical blind loop, previous ileo-caecal resections, post-radiation enteropathy, small intestinal pseudo-obstruction, small intestinal bacterial overgrowth syndrome (see e.g. Kopacova, “Small intestinal bacterial overgrowth syndrome”, 2010, Vo. 16, No. 24, pages 2978-2990 and Quigley E M and Abu-Shanab A, “Small intestinal bacterial overgrowth”, Infect Dis Clin North Am, 2010, Vol. 24, No. 4, pages 943-59), autonomic neuropathy including autonomic neuropathy in type 2 diabetes (see e.g. Bures et al., “small intestinal bacterial overgrowth syndrome”, 2010, World J Gastroenterol, Vol. 16, No. 24, pages 2978-2990), vaginal mycosis and intestinal mycosis (see e.g. Achkar and Fries, “Candida infections of the genitourinary tract”, 2010, clinical microbiology reviews, Vol. 23, pages 253-273), multiple system atrophy, food intolerance, intestinal infections, gallstones and hyperactivity of the immune system.
As mentioned below, dysbiosis is known to affect the upper and mid GI tract including the stomach, the small intestine and the colon. If classified according to the region in the GI tract, achlorhydria is linked to dysbiosis in the stomach, whereas the following diseases are linked to dysbiosis in the small intestine: pancreatic exocrine insufficiency, small intestinal bacterial overgrowth syndrome, small intestinal pseudo-obstruction, surgical blind loop, small intestinal obstruction, scleroderma, food intolerance and hyperactivity of the immune system. The following diseases are linked to dysbiosis in the colon: colorectal cancer, ulcerative colitis, diverticulitis, Parkinson's disease and fistulae, whereas the following diseases are linked to dysbiosis in the colon and the small intestine: Crohn's disease, previous ileo-caecal resection, post-radiation enteropathy, autonomic neuropathy including autonomic neuropathy in type 1 and 2 diabetes, intestinal infections and intestinal mycosis. The following diseases are also linked to dysbiosis, wherein there appears to be no link to a specific region in the GI tract: obesity, autism, metabolic syndrome, rheumatoid arthritis, allergy, diabetes mellitus including type 2 diabetes and sepsis.
Thus, intestinal dysbiosis is present in the above mentioned patient population suffering from i) pain and ii) at least one further disease selected from the diseases outlined above.
The intestinal microbiota carries out important effects such as protective, structural and metabolic effects on the intestinal mucosa. The main functions appear to be the following: a protective function (pathogen displacement, nutrient competition, receptor competition, production of anti-microbial factors), a structural function (barrier fortification, induction of IgA, apical tightening of tight junctions, immune system development) and a metabolic function (control of epithelial cell differentiation and proliferation, metabolism of dietary carcinogens, synthesis of vitamins, fermentation of non-digestible dietary residue and epithelial-derived mucus, iron absorption, salvage of energy).
Intestinal dysbiosis therefore results in an impairment or even complete loss of the above functions and may particularly manifest in changes in the metabolic profile, gas production, impairment of GI transit, epithelial barrier dysfunction, pathogen overgrowth and mucosal immune equilibrium changes.
A patient suffering from at least one disease iii) as defined above is particularly susceptible for increased intestinal bacterial translocation and thus developing peritonitis, SIRS and/or sepsis. Generally, patients with an impaired liver function, e.g. due to cirrhosis or hepatitis, particularly hepatitis B and C, are at higher risk for an increased intestinal bacterial translocation and thus e.g. for peritonitis. This is also the case for patients suffering from chronic kidney disease. A particular patient population being at increased risk for an increased intestinal bacterial translocation and thus e.g. for peritonitis corresponds to patients undergoing peritoneal dialysis, e.g. as a treatment form of chronic kidney disease. Also, patients suffering from an infection in a specific organ, which may spread, are at higher risk for increased intestinal bacterial translocation resulting in peritonitis, SIRS and/or sepsis. Such patients may e.g. suffer from appendicitis, pancreatitis, and cholecystitis. It should be noted that patients suffering from Crohn's disease and diverticulitis, which are listed above under diseases resulting in intestinal dysbiosis, may also be at increased risk for increased intestinal bacterial translocation and thus e.g. may develop peritonitis, SIRS and/or sepsis.
Patients suffering from at least one disease iii) are thus particularly vulnerable to increased bacterial translocation and even a low number of bacterial translocation may suffice to actually induce peritonitis, SIRS and/or sepsis. If such a patient additionally suffers from pain, a pain treatment should be selected, which fails to further increase the risk of peritonitis, SIRS and/or sepsis, e.g. by inducing an increased bacterial translocation.
Efficient pain treatment, particularly treatment of moderate to severe pain, can generally be achieved by the administration of opioid analgesics, such as e.g. morphine or oxycodone. However, the administration of opioid analgesics may result in undesirable side effects, including undesirable side effects in the GI tract. Particularly prominent side effects are opioid-induced constipation (OIC) and opioid-induced bowel dysfunction (OIBD). Further, as inter alia shown herein, the administration of opioid analgesics also negatively affects the intestinal microbiota and results in an increased bacterial translocation.
It is important to note that no correlation or link between OIC or non-opioid induced constipation and intestinal dysbiosis has been established thus far. This is inter alia confirmed e.g. by the definition of the term “dysbiosis” in Wikipedia as recited above, wherein no link between constipation and dysbiosis is made. Rather, constipation is known as developing in the lower GI tract (the colon) only, whereas dysbiosis also affects the upper and mid GI tract including the stomach. Thus, e.g. achlorhydria linked to dysbiosis in the stomach or e.g. pancreatic exocrine insufficiency or small intestinal bacterial overgrowth syndrome linked to dysbiosis in the small intestine are completely unrelated to constipation and no conclusion or transfer can be made from constipation in the colon to any of these diseases. Further, it appears that constipation is not a precondition for intestinal dysbiosis; to the contrary, intestinal dysbiosis may be present without any constipation or even cause constipation.
Since OIC corresponds to a well-known side effect of opioid analgesic therapy, a physician confronted with the above mentioned patient population (in which intestinal dysbiosis is present and/or which is particularly vulnerable to bacterial translocation), will likely be reluctant to administer an active agent, for which a further worsening of a GI parameter, namely constipation, is known. Moreover, opioid analgesic therapy has a further negative impact on the intestinal dysbiosis and increases the risk for bacterial translocation, as shown in the present application and as discussed in the next paragraphs. In consequence, this will result in the undertreatment of pain in such patients since a physician is reluctant to prescribe the administration of e.g. oxycodone alone.
Alternatively, if the physician decides to administer an opioid analgesic in order to treat pain, the additional administration of an active agent alleviating the intestinal dysbiosis appears advisable in order to preemptively counter the further worsening of GI parameters. Such an additional therapy may reside in the administration of probiotics such as e.g. lactic acid bacteria or Bifidobacteria to improve dysbiosis. In case of a pain patient being particularly susceptible for peritonitis, the additional administration of an active agent decreasing this susceptibility appears advisable in order to preemptively address a possible peritonitis. Such an additional therapy may reside in the administration of antibiotics. Furthermore, it might even be advisable under the above circumstances to administer an active agent symptomatically counteracting the OIC, such as e.g. a laxative.
Clearly, either the undertreatment of pain or the additional administration of further active agents, which cause further side effects and additional direct or indirect costs (e.g. to treat or manage side effects, costs of additional medication) next to the opioid analgesic is undesirable.
The present inventors have now surprisingly found that the administration of a combination of the opioid agonist oxycodone and the opioid antagonist naloxone solves the above problem: the results of example 3 of the present application inter alia show that the administration of oxycodone alone results in i) a decrease in the body weight, ii) an increased translocation of bacteria into mesenteric lymph nodes, iii) a major change of the microbiome (in this case the bacterial composition) in the small intestine and the colon (wherein the fraction of pathogenic bacteria such as proteobacteria is increased), and iv) an upregulation of TLR2 in the small intestine (determined in the jejunum). All these effects induced by oxycodone are at least partly reversed by naloxone. Thus, as regards i), the decrease of the body weight is clearly not as pronounced if the combination of oxycodone and naloxone is administered; this may be due to differences in the GI microbiome and/or inflammatory reactions in the GI wall induced with oxycodone only. As regards ii), the addition of naloxone completely reverses the increased translocation induced by oxycodone to normal levels. It can be speculated that the effect ii) observed upon administration of oxycodone is linked to the observation iv) above. Thus, an increase in TLR2 activity appears to be involved in mucosal barrier defects that result in increased bacterial translocation into the mesenteric lymph nodes (see also Meng et al., “Morphine induces bacterial translocation in mice by compromising intestinal barrier function in a TLR-dependent manner”, PLOS ONE, 2013, 8(1): e54040; the authors describe results observed with morphine, see below). The TLR2 levels are not increased upon administration of the combination of oxycodone and naloxone; accordingly, due to the presence of naloxone, TLR2 expression is not increased and, likely linked thereto, no increased bacterial translocation into mesenteric lymph nodes takes place.
Summarizing the above, oxycodone has several negative effects on the microbiome of the GI tract which manifest in or include a decrease in body weight, adverse changes in the microbiome towards pathogenic populations (particularly in the small intestine), and an increased translocation of bacteria into mesenteric lymph nodes (particularly in the small intestine). Particularly the adverse changes of the microbiome together with an impaired mucosal barrier function, both of which are observed upon administration of oxycodone, may result in severe infections ascending from the small intestine. This is of course particularly true if a patient already suffers from a disease negatively influencing the GI tract, i.e. a disease resulting in intestinal dysbiosis or an increased risk in peritonitis. It is noteworthy that studies with morphine in mice and rats also strongly suggest that morphine has a negative effect on the microbiome and the intestinal barrier function (see Meng et al. supra; Nieuwenhuijs et al., “The role of interdigestive small bowel motility in the regulation of gut microflora, bacterial overgrowth, and bacterial translocation in rats”, Annals of Surgery, 1998, Vol. 228, No. 2, 188-193; Babrowski et al., “Pseudomonas aeruginosa virulence expression is directly activated by morphine and is capable of causing lethal gut-derived sepsis in mice during chronic morphine administration”, Annals of Surgery, 2012, Vol. 255, No. 2, 386-393).
Thus, the combination is not only effective in counteracting the side effect OIC while maintaining analgesia without any substantial loss in the actual analgesia, but is also suitable for improving intestinal dysbiosis or at least not further worsening intestinal dysbiosis. This is achieved by the presence of naloxone in the combination, which has a positive effect particularly on the intestinal microbiome and results in a restored intestinal barrier function. This positive effect has been discussed above and can inter alia be derived from the results shown in example 3 of the present application.
The actual treatment of pain with a combination of oxycodone and naloxone is thus possible in the patient population with intestinal dysbiosis while the intestinal dysbiosis may even be improved or at least not further worsened; accordingly, the administration of additional active agents would be unnecessary with respect to the improvement of intestinal dysbiosis or OIC. A corresponding pain treatment regime in the patient population as set out above may thus rely on the administration of a dosage form comprising oxycodone and naloxone only.
Further, the combination of oxycodone and naloxone fails to induce an increased bacterial translocation and is thus even suitable for lowering the susceptibility particularly for peritonitis, SIRS and/or sepsis. As noted above, naloxone is responsible for counteracting the negative effect on the intestinal barrier function induced by oxycodone. The combination may thus also particularly be used in pain patients with an increased susceptibility for peritonitis, SIRS and/or sepsis as a prophylactic measure against an actual peritonitis, SIRS and/or sepsis. The administration of additional prophylactic active agents such as antibiotics would thus be unnecessary with respect to the prophylaxis of peritonitis, SIRS and/or sepsis if a combination of oxycodone and naloxone is administered. Pain treatment in a patient population suffering from pain and having an increased risk for intestinal bacterial translocation may thus rely on the administration of a dosage form comprising oxycodone and naloxone only.
More generally, one may thus refer to pain treatment by the combination of oxycodone and naloxone as efficient pain management while improving GI parameters; this not only refers to GI parameters in the lower GI tract, such as e.g. OIC, but also to GI parameters in the upper and mid GI tract (including the stomach and the small intestine), such as e.g. intestinal dysbiosis or an increased risk of bacterial translocation. An analysis of GI parameters in the upper and mid GI tract may inter alia be carried out by a quantitative analysis of intestinal microbiota, the orocaecal transit time, bacterial translocation and gastric emptying or parameters such as e.g. the intestinal and serum metabolome, the abdominal girth, stool consistency (using the Bristol Stool From Scale), immune and inflammatory responses, and correlations between said parameters. For correlation reasons, the analysis of parameters of the lower GI tract, such as e.g. OIC, may be included.
One may thus refer to the combination of oxycodone and naloxone as being suitable for the treatment of pain while not only improving OIC (and consequences of OIC such as hemorrhoids or hemorrhoidal bleeding) but also opioid-induced bowel dysfunction in the upper and mid GI tract. Opioid-induced bowel dysfunction may also be referred to as “GI dysfunction”.
Release Behavior of the Dosage Form
In general, the release behavior of a dosage form can inter alia be determined by an in vitro release test.
In this regard, the term “in vitro release” refers to the release rate at which a pharmaceutically active agent, e.g. oxycodone HCl, is released from the pharmaceutical composition when the in vitro release rate is tested by the paddle method according to the European Pharmacopeia as described in the Ph. Eur. 2.9.3 6th edition. The paddle speed is set at 100 rpm in simulated gastric fluid (SGF) dissolution medium with pH 1.2. Aliquots of the dissolution media are withdrawn at the respective time points and analyzed by HPLC with a C18 column, eluted with 30 mM phosphate buffer in acetonitrile (70:70; pH 2.9) with a flow rate of 1.0 ml/min and detected at 220 nm. The term “Simulated Gastric Fluid, pH 1.2” refers to 0.1 N HCl, pH 1.2.
In contrast to an “immediate release”, a “prolonged release” dosage form in accordance with the present invention refers to pharmaceutical compositions which release in vitro≤75% (by weight) of the pharmaceutically active agents, namely oxycodone and naloxone, at 45 min.
In the context of the present invention, the term “immediate release” refers to pharmaceutical compositions showing a release of the active substance(s) which is not deliberately modified by a special formulation design and/or manufacturing methods. For oral dosage forms this means that the dissolution profile of the active substance(s) depends essentially on its (theirs) intrinsic properties. Typically, the term “immediate release” refers to pharmaceutical compositions which release in vitro>75% (by weight) of the pharmaceutically active agent(s) at 45 min.
Prolonged release properties may be obtained by different means such as by a coating which is then designated as a prolonged release coating, a matrix which is then designated as a prolonged release matrix or e.g. by an osmotic structure of the pharmaceutical composition.
In order to obtain “prolonged release” properties, one typically uses materials which are known to prolong the release from a dosage form comprising e.g. a prolonged release matrix and/or prolonged release coating. Typical examples are set out further below. The nature of the “prolonged release material” may depend on whether the release properties are attained by a “prolonged release matrix” or a “prolonged release coating”. The term “prolonged release materials” thus describes both types of materials. The term “prolonged release matrix material” indicates that a material is used for obtaining a prolonged release matrix. Likewise, the term “prolonged release coating material” indicate that a material is used for obtaining a prolonged release coating.
The term “prolonged release matrix formulation” refers to a pharmaceutical composition including at least one prolonged release material, and at least oxycodone and naloxone as the two pharmaceutically active agents. In a “prolonged release matrix formulation”, the “prolonged release materials” are combined with the pharmaceutically active agents to form a mixture from which the pharmaceutically active agents are released over prolonged periods of time, such as e.g. 8, 10, 12, 14, 16, 18, 20, 22 or 24 hours.
It is to be understood that a material will be considered to act as prolonged release material if the dissolution profile of the pharmaceutically active agents is slowed down compared to an immediate or conventional release formulation. If a prolonged release material can be used for manufacturing a prolonged release matrix, it will be considered as a prolonged release matrix material.
Pharmaceutically acceptable excipients which are used to adjust an already prolonged release to a specific profile are not necessarily considered to be prolonged release materials.
It is to be understood that a prolonged release matrix does not necessarily consist only of the pharmaceutically active agents and the prolonged release material. The prolonged release matrix may comprise in addition pharmaceutically acceptable excipients such as fillers, lubricants, glidants, etc. Examples of such excipients are set out below.
The term “prolonged release coating formulation” refers to a pharmaceutical composition including at least one prolonged release material, and oxycodone and naloxone as the two pharmaceutically active agents. In a “prolonged release coating formulation”, the “prolonged release materials” are disposed on the pharmaceutically active agents to form a diffusion barrier. Other than in prolonged release matrix formulation, the actives are not intimately mixed with the prolonged release material and the prolonged release coating does not form a three dimensional structure within which the actives are distributed. As the term implies, the prolonged release material forms a layer above the actives. The pharmaceutically active agents are released from a prolonged release coating formulation over prolonged periods of time, such as e.g. 8, 10, 12, 14, 16, 18, 20, 22 or 24 hours.
It is to be understood that a material will be considered to act as prolonged release material if the dissolution profile of the pharmaceutically active agents is slowed down compared to an immediate or conventional release formulation. If a prolonged release material can be used for manufacturing a prolonged release coating, it will be considered as a prolonged release coating material.
Pharmaceutically acceptable excipients which are used to adjust an already prolonged release to a specific profile are not necessarily considered to be prolonged release materials.
When it is mentioned that a prolonged release coating is disposed on pharmaceutically active agents, this is not to be construed as meaning that such a coating will necessarily be directly layered on such active pharmaceutically agents. Of course, if the pharmaceutically active agents oxycodone and naloxone are layered on a carries such as nu-Pareil beads, the coating may be disposed directly thereon.
However, the pharmaceutically active agents may also be first embedded in a polymer layer or e.g. a prolonged release matrix. Subsequently the prolonged release coating may be disposed on e.g. granules which comprise a prolonged release matrix or on tablets which are made from such granules by compression for example.
A pharmaceutical composition with a prolonged release coating may be obtained by combining the pharmaceutically active agents with a carries such as non-Pareil beads and disposing a prolonged release coating on said combinations. Such coating may be made from polymers such cellulose ethers with ethyl cellulose being preferred, acrylic resins, other polymers and mixtures thereof. Such prolonged release coatings may comprise additional excipients such as pore-formers, binders and the like.
It is further to be understood, that the term “prolonged release matrix formulation” does not exclude pharmaceutical compositions with a prolonged release matrix and an additional prolonged release coating being disposed on the matrix. Likewise the term “prolonged release coating formulation” does not exclude pharmaceutical compositions with a prolonged release coating which is disposed on prolonged release matrix.
The term “prolonged release dosage form” refers to the administration form of a pharmaceutical composition of the present invention comprising the two pharmaceutically active agents, i.e. oxycodone and naloxone, in prolonged release form as e.g. in form of a “prolonged release matrix formulation”, in the form of a “prolonged release coating formulation”, combinations thereof or in other prolonged release formulations such as osmotic formulations. The terms “prolonged release matrix formulation” and “prolonged release dosage form” can be used interchangeably if the prolonged release dosage form consists essentially of the prolonged release matrix formulation. This means that a prolonged release dosage form can comprise in addition to the prolonged release matrix e.g. cosmetic coatings and pharmaceutically acceptable excipients such fillers, lubricants, etc.
For some embodiments, the term “prolonged release matrix dosage form” may indicate that the dosage form comprises a prolonged release matrix as the sole structure being responsible for prolonging the release. This, however, does not exclude that the dosage form may comprise an immediate release portion.
For some embodiments, the term “prolonged release coating dosage form” may indicate that the dosage form comprises a prolonged release coating as the sole structure being responsible for prolonging the release. This, however, does not exclude that the dosage form may comprise an immediate release portion.
The release rates indicated always refer to the formulation such as a monolithic tablet or multi-particulates. The release rates will be chosen such that a pharmaceutical composition can be administered e.g. on a twice a day or once a day basis, i.e. every 12 hours or every 24 hours. Typically, the release will occur by diffusion through the prolonged release matrix and/or coating, erosion of the prolonged matrix and/or coating or combinations thereof.
Release Materials
The following description of suitable materials is to be understood as being not limiting. Rather, the release material may be any material that is known to be capable of imparting prolonged release properties on the active agents, oxycodone and naloxone, when being formulated into a dosage form.
Prolonged Release Matrix Materials
Suitable materials for inclusion in a prolonged release matrix in order to provide a prolonged release matrix dosage form comprising an opioid agonist and an opioid antagonist include:
In a preferred embodiment, the pharmaceutical dosage forms as described in the present invention will use a diffusion matrix for achieving prolonged release of oxycodone and naloxone from the pharmaceutical dosage form.
To this end, the diffusion matrix may be made from a hydrophobic polymer and/or a C12-C36 fatty alcohol.
As regards the hydrophobic polymer, use of a hydrophobic cellulose ether and particularly ethyl cellulose may be preferred.
As regards the fatty alcohol, use of lauryl, myristyl, stearyl, cetylstearyl, ceryl and/or cetylalcohol will be preferably considered. The use of stearyl alcohol is particularly preferred.
A particularly preferred embodiment relates to pharmaceutical dosage forms in which the prolonged release properties of oxycodone and naloxone are provided by a diffusion matrix which is made from a hydrophobic polymer such as from ethyl cellulose and a fatty alcohol. The matrices of some of the preferred embodiments of the invention, which may e.g. be made from the aforementioned combination of ethyl cellulose and stearyl alcohol, will be a substantially non-swellable diffusion matrix.
The term “substantially non-swellable diffusion matrix” indicates that the matrix will be substantially non-erosive, i.e. that the size of the matrix will not significantly increase upon contact with fluids. Typically, the volume of a substantially non-swellable diffusion matrix will increase at maximum up to 100%, preferably at maximum up to 75%, more preferably at maximum up to 50%, even more preferably at maximum up to 25% and most preferably at maximum up to 10% or at maximum up to 5% in volume upon contacting an aqueous solution.
Pharmaceutical dosage forms which comprise a hydrophobic polymer with hydrophobic cellulose ethers such as ethyl cellulose being preferred as the sole or one of the components for providing a prolonged release (non-swellable) diffusion matrix, will use an amount of such polymer of between 5 to 20%, preferably of between 6 and 15% by weight and more preferably of between 7 to 10% by weight. The percentages indicate the amount of the matrix-forming material with respect to the total weight of the pharmaceutical dosage form.
Pharmaceutical dosage forms, which comprise a fatty alcohol as the sole or one of the components for providing a prolonged release diffusion matrix, will use an amount of fatty alcohol in the matrix of between 10 to 40%, preferably of between 15 to 35% and more preferably of between 17 to 25% by weight. These percentages again indicate the amount of fatty alcohol based on the total weight of the dosage form.
The person skilled in the art is further aware that such a prolonged release matrix may also contain other pharmaceutically acceptable ingredients and excipients which are conventional in the pharmaceutical art such as lubricants, fillers, binders, flowing agents, colorants, flavorings, surfactants, pH-adjusters, anti-tacking agents and granulating aids. These excipients will typically have no substantial impact on the overall release behavior of the pharmaceutical dosage form.
Typical examples of fillers (diluents) comprise lactose, preferably anhydrous lactose, glucose, saccharose, starch and their hydrolysates, microcrystalline cellulose, cellatose, sugar alcohols such as sorbitol or mannitol, calcium salts like calcium hydrogen phosphate, dicalcium- or tricalcium phosphate. Granulating aids comprise inter alia povidone. Flowing agents and lubricants comprise inter alia highly dispersed silica, talcum, magnesium oxide, calcium stearate, magnesium stearate, sodium stearyl fumarate, fast like hydrated castor oil and glyceryl dibehenate. Binders can include hyproxypropylmethyl cellulose (hypromellose), hydroxypropyl cellulose (HPC), hydroxyethyl cellulose, polyvinyl pyrollidone (povidone), acetic acid vinyl ester (copovidone) and carboxymethycellulose sodium. Anti-tacking agents may include glycerol monostearate. Furthermore, a matrix-based dosage form may e.g. comprise a cosmetic coating.
Prolonged Release Coating Materials
As mentioned above, prolonged release characteristics of a pharmaceutical dosage form may also be achieved by a film coating that governs the release of the active agents from the dosage form. To this end, the pharmaceutical dosage form may comprise a carrier, which is associated with the oxycodone and naloxone. For example, one may use nonpareil beads, sugar beads etc. on and/or into which the pharmaceutically active agents are disposed.
Such active-associated carriers may then be overcoated with a coating that provides prolonged release characteristics. Suitable prolonged release coating materials include hydrophobic polymers such as cellulose ethers and/or acrylic polymer resins. Ethylcellulose may be preferred.
The prolonged release coatings may comprise other components such as hydrophilic substances including hydrophilic polymers such hydroxypropylmethylcellulose (HPMC), polyethylenglycols etc. These components may be used to adjust the prolonged release characteristics of the coatings. In case of e.g. HPMC, the substances may act as pore formers. The coating may, of course, also comprise additional pharmaceutically acceptable excipients, e.g. as set out above for the matrices.
Immediate Release Materials
Typical pharmaceutically acceptable excipients used in immediate release dosage forms are disintegrants, diluents, lubricants, glidants, anti-tacking agents, plasticizers, colorants, flavorants, binders, pH adjusters and the like. These excipients (with the exception of disintegrants) are to be chosen such that they do not substantially alter the immediate release in vitro release rates.
It can be preferred for the pharmaceutical compositions of the present invention to comprise at least a diluent and optionally a disintegrant as pharmaceutically acceptable excipients, particularly if the pharmaceutical compositions of the present invention are provided as a tablet. It can also be preferred for the pharmaceutical compositions of the present invention to comprise at least a disintegrant and optionally a diluent as pharmaceutically acceptable excipients, particularly if the pharmaceutical compositions of the present invention are provided as a tablet. It can further be preferred to use excipients which act both as a disintegrant and a diluent.
The disintegrant, for example, will ensure that the tablet after administration will rapidly disintegrate so that the active agents become readily available for absorption.
Diluents may be selected from but are not limited to lactose such as lactose monohydrate, lactose anhydrous, starch such as maize starch, pregelatinized starch, microcrystalline cellulose, glucose, Mannitol, Maltitol, StarLac® (85% spray dried lactose, 15% maize starch), saccharose, calcium salts like calcium hydrogen phosphate or any combinations of the above.
Disintegrants may be selected from but are not limited to inter alia StarLac® (85% spray dried lactose, 15% maize starch), croscarmellose such as croscarmellose sodium, sodium starch glycolate, crospovidone, alginic acid, or low substituted hydroxypropyl cellulose.
A combination of lactose and starch such as the Starlac® product can be particularly preferred as it combines the properties of a filler and a disintegrant.
Glidants and lubricants may be selected but are not limited to inter alia highly dispersed silica, talcum, magnesium oxide, magnesium stearate, sodium stearyl fumarate etc.
Flowing agents and lubricants comprise inter alia highly dispersed silica, talcum, magnesium oxide, magnesium stearate, sodium stearyl fumarate etc.
If pharmaceutical compositions of the present invention are provided as a tablet, they may be coated for identification purposes with a cosmetic coating. Such coatings will have no substantial impact on the immediate release properties of the pharmaceutical compositions in accordance with the invention.
Preferably, one can use a combination of e.g. starch and lactose as disintegrant. Lactose alone may at the same time function as a filler. A particularly preferred embodiment relies on the product Starlac®, a combination of lactose 85% and starch 15%, which may function both as a disintegrant and as a filler. The combined filler/disintegrant may be comprised within the pharmaceutical composition in an amount of about 40% to about 90%, preferably in an amount of about 50% to about 85% and even more preferably in an amount of about 60% to about 80% by weight based on the weight of the composition. These numbers particularly apply if an excipient having a dual function both as a disintegrant and a filler such as Starlac® is used.
Further particularly preferred embodiments of the present invention are mentioned in the following:
Influence of codeine on the gastrointestinal (GI) microbiota, the GI metagenome (i.e. the whole genetic information of the microbial community) and the host metabolome (i.e. products and/or metabolites produced by the microbial community).
The main goal of this example resides in the determination of upper and mid GI activity and structural integrity and several GI microbiota parameters including metabolomic parameters of plasma (as a result of bacterial metabolism in the upper/mid GI tract) in healthy subjects comparing the situation prior to and after opioid administration (see also
Ten healthy volunteers will be recruited and a codeine-dose of 120 mg/d (30 mg four times daily) will be given for ten days. Diet will not be restricted and the bowel/stool behavior will be noted daily by the volunteers. Before the first dose and after the last dose, individuals will undergo upper- and lower-GI tract endoscopy and luminal contents and mucosal biopsies will be taken. Luminal contents will additionally be preserved with glycerol for subsequent transplantation into gnotobiotic mice (see Example 2). Plasma and urine samples will be collected. Volunteers will also undergo a H2 breath test with oral lactulose to assess microbial metabolic activity (especially methane production) and orocoecal transit time. Since bowel preparation for lower GI endoscopy influences the results of H2 breath tests, only a sigmoidoscopy without previous oral lavage will be performed for these experiments.
All of the following objectives are based on the comparison between day 0 and day 10 (see also
Objective 1: Comparison of the small-bowel microbiota based on comparative 16S rDNA-based microbial community profiling.
Objective 2: Comparative metagenome and metatranscriptome (i.e. the transcriptome of the microbiota) analyses of individual samples (luminal contents only).
Objective 3: Comparative metabolome analyses by assessing the plasma and urine-samples for metabolome signatures based on MS-techniques. The comparison of the metabolome spectra will reveal altered metabolite profiles, which may then be correlated to changes in the individual metagenomes/metatranscriptomes to identify the molecular basis of microbiota caused changes in metabolism.
Objective 4: Assessing the epithelial barrier function of mucosal biopsies and performing a mucosal immune-phenotyping based on IHC and FACS; assessing of selected targets of barrier function (such as e.g. claudins) and the mucosal immune system (pro- vs. anti-inflammatory) based on qRT-PCR.
Objective 5: Transplantation of microbiota into gnotobiotic mice and analysis of gut motility, mucosal barrier function and the mucosal immune-system on the basis of this animal-model.
Influence of oxycodone/naloxone on murine gut function, the GI microbiota and the gut-brain axis.
The main goal of this example resides in the determination of GI microbiota parameters and GI structural parameters including impact on local and systemic immune response/inflammation influenced thereby in an animal model comparing the effects of codeine, oxycodone, naloxone and oxycodone/naloxone on said parameters.
C57BL/6 mice (n=10/group) will receive either codeine (40 mg/kg twice daily), oxycodone (10 mg/kg twice daily) or naloxone (15 mg/kg twice daily), alone or in combination, by gavage for 10 days, the readouts being taken during days 8 to 10. A washout experiment will be conducted in which the mice will first be treated with the opioid agonist or antagonist for 10 days, followed by a 20 day washout period, the readouts being taken during days 18 to 20 of the washout period.
Objective 1: After sacrifice, GI specimen (stomach, upper small intestine, lower small intestine, caecum and colon) will be taken and comparative 16S rDNA-based microbial community profiling will be performed.
Objective 2: To test for GI transit time, expulsion of carmine red-stained faeces following transgastric administration of carmine red by gavage will be assessed. Further, to test for mucosal permeability, blood to gut lumen ratio of rhodamine-dextran following intragastric administration of rhodamine-dextran by gavage will be assessed.
Objective 3: To assess the impact of treatment on the gut-brain axis in the different experimental groups, corresponding tests will be performed with the animals: pain sensitivity, anxiety-like behavior, depression-like behavior and activity of the hypothalamus-pituitary-adrenal axis activity. Further, immunological parameters such as spleen weight and plasma levels of cytokines such as IL-6 will be assessed.
Effects on intestinal microflora composition and bacterial translocation following multiple oral doses of oxycodone and oxycodone/naloxone combination in male C57BL/6 RAG1 knockout mice.
The main goal of this example resides in the determination of several GI microbiota parameters and GI structural parameters including impact on local and systemic immune response/inflammation in an animal model comparing the effects of oxycodone and oxycodone/naloxone on said parameters to baseline and placebo.
Groups and dosing regimens are depicted in
Male mice of the strain C57BL/6 RAG −/− (Taconic Model 4175-M, Taconic Laboratories) with an approximal weight at arrival of 20±7 g at an approximal age of 5 to 10 weeks were used in the present study.
Appropriate amounts of oxycodone and naloxone were dissolved in sterile water to make two dose formulations containing the following nominal concentrations of oxycodone and naloxone: (i) 1 mg/mL Oxycodone and (ii) 1 mg/mL Oxycodone+0.5 mg/mL Naloxone. The formulations were prepared on Day 0 and used for Day 1 to Day 8 dosing. Sterile water was used as vehicle. Each of the two dose formulations was transferred into eight individual sterile vials through sterilization filters, one designated for each day of dosing. The dose formulations were stored refrigerated and protected from light.
Dosing Procedures:
Animals were administered the dose by oral gavage three times a day (˜4 hours apart) for 7 days and once on the 8th day. Prior to the first dose administration of the day, the dose formulation vials designated for that day were removed from the refrigerator, briefly mixed, and allowed to come to room temperature, where the vials remained throughout the day. After the third dose on day 7, all animals fasted through euthanasia. The dose volume was based on the animal's body weight on Day 1. Dose volume was recorded.
Observation of Animals:
Antemortem Observations
During the post-dose, in-life portion of the study, observation of animals for general health and mortality were performed twice daily (AM and PM) on weekdays and once daily on weekends. During the acclimation period, animals were observed once daily. Only healthy animals were dosed.
Body Weights
Individual body weights were recorded prior to administration of the first dose on Day 1. The body weight determinations prior to Day 1 dose administration was used to determine the dose administered for all subsequent doses. Subsequent body weights were recorded daily after the 2nd dose of the day on Days 2 through 7.
Sample Collection:
Groups 2, 4, and 5: Charcoal Test of Intestinal Motility
Fifteen minutes after the eighth day morning dosing, 0.1 mL of charcoal suspension (5% activated charcoal powder, 10% gum Arabic in water) were delivered to the stomach of each mouse using a gavage needle.
Thirty minutes after charcoal delivery, animals were euthanized by an overdose of CO2. The abdominal cavity of each mouse was opened and the edge of the charcoal meal was tied off. The entire small intestine (from the stomach at the pylorus to the caecum) was removed. Its full length and the length of charcoal meal traveled were measured in centimeters. Intestinal transit was expressed as the percentage of intestine length containing the meal, i.e. 100×(pylorus to meal front/pylorus to caecum length). Following measurements, the small intestine was discarded, along with the carcass.
Groups 1, 3, 6, and 7: Serum; Mesenteric Lymph Nodes; Gastrointestinal Tract Luminal Content and Mucosal Scrapings
In order to minimize contamination during sample collection, the following measures were invoked:
Immediately after the eighth day dosing, each animal was anesthetized with CO2 and blood (maximum obtainable volume) was collected by cardiac puncture into a syringe. Blood was transferred into centrifuge tubes and allowed to clot at room temperature for a minimum of 5 minutes, after which the blood was centrifuged for 10 min at 10,000 rpm at room temperature. Serum was collected and placed on dry ice prior to storage in a −80° C. freezer. Following blood collection, animals were euthanized via CO2 overdose.
Mesenteric Lymph Nodes (MLNs)
Following euthanasia, the abdomen was opened. The mesenteric root was presented and the mesenteric net unfolded. The mesenteric lymph nodes (MLNs) were removed and surrounding fat was removed. The MLNs were then weighed into sterilized tubes. Following weighing, the MLNs were frozen in liquid nitrogen. Following freezing, the MLNs were placed on dry ice prior to storage in a −70° C. freezer (lymph nodes at −20° C.).
Stomach and Intestine
Following removal of the mesenteric lymph nodes, the gastrointestinal tract (from the stomach through the colon) was removed. The intestine was uncoiled with removal of mesenteric adhesions. The gastrointestinal tract was divided into the following sections: stomach; small intestine; caecum; colon. The stomach was discarded. The small intestine was spread in a meandering pattern and the colon was spread to its length. The small intestine and colon were placed alongside a ruler or similar reference, and photographed separately. The lengths of the small intestine and colon were recorded.
Luminal Contents (Small Intestine, Caecum, Colon)
The small intestine, caecum, and colon were cut longitudinally. The contents of each were individually collected into separate containers with a small spatula or similar instrument, taking care to cause as little injury to the tissue as possible. The weight of the contents collected from each portion was recorded. The weights of the small intestine, caecum, and colon following removal of the contents were also recorded. Collected luminal contents samples were then frozen in liquid nitrogen. Luminal contents samples were then placed on dry ice before transfer to a −80° C. freezer.
Mucosal Scraping (Small Intestine, Caecum, Colon)
A buffer solution for collection, storage, and shipment of collected mucosal scraping samples was prepared: RLT buffer (Qiagen; catalog number 79216) was fortified with 1% beta-Mercaptoethanol (Applichem; catalog number A1108) and thoroughly mixed, then filter sterilized into a sterile RNAse free Eppendorf cup, yielding sterile mucosal scraping buffer solution.
Following removal of the luminal contents from the small intestine, caecum, and colon, the small intestine were divided into the duodenum, jejunum, and ileum. Residual luminal content was removed from the duodenum, jejunum, ileum, caecum, and colon by swaying in phosphate buffered saline (PBS) 10% fetal calf serum (FCS) at approximately 37° C. Following removal of residual luminal contents, an approximately 2 cm length of the mucosa was separated from the remaining tissue by sweeping or scraping along the luminal tissue from proximal to distal using a long thin metal spatula or similar instrument. These mucosal scrapings were collected separately by organ (duodenum, jejunum, ileum, caecum, colon) and weighed into individual sterilized Eppendorf CABE safelock snap-cap tubes or similar containing 350 μL of the prepared sterile mucosal scraping buffer solution. The tubes were closed, vortexed, and the samples frozen in liquid nitrogen. Samples were then placed on dry ice before transfer to a −80° C. freezer. Remaining gastrointestinal tissue was discarded, along with the carcasses.
Read Out: The body weight was assessed daily; for the baseline group and the study end, the following parameters will be determined: length and weight of intestine/intestinal microbiota composition by 16SrDNA (small intestine and caecum)/microbial count in mesenteric lymph nodes (translocation)/concentration of LPS, sCD14, LBP, TNF-α (heart blood)/IL-6, TNFα mRNA expression in mucosal scrapings (small intestine, colon, caecum)/metabolome analysis.
Results:
Charcoal Test of Intestinal Motility
The results of the study relating to GI transit are shown in
Body Weights
The results of the body weights over 7 days are shown in
Analysis of the Mesenteric Lymph Nodes (as Parameter for Bacterial Translocation)
MLNs were obtained as indicated above and the amount of bacteria in the MLNs was analyzed by determining colony forming units (CFUs) per g MLN in different media and under different conditions as indicated in
Analysis of the Contents of the Small Intestine
The contents of the small intestine of the different groups were obtained as described above. The presence and the amount of bacteria of different phyla was then determined in the oxycodone (G6) and in the oxycodone/naloxone (G7) treated groups according to standard methods. The results are shown in
As can be derived from the graph of the G6-group, there is a clear increase in (pathogenic) proteobacteria compared to the G7-group. This increase has thus far not been described as a result of the administration of oxycodone. Further, a clear decrease in bacterioides in the G6-group compared to the G7-group can be observed. Again, such a change has thus far not been described as a result of the administration of oxycodone. Naloxone is capable of reversing these negative changes in the bacterial composition induced by oxycodone.
The results of the small intestine samples are shown in the following on an individual level for the mice of the two different groups (n=7 for G6 [oxycodone only] and n=4 for G7 [oxycodone/naloxone]).
As can be derived from the above table, the two mice 03-SI and 04-SI of the G6-group show a completely altered small intestine composition hardly displaying any bacteroidetes but rather firmicutes and also proteobacteria. It is noted that mice 03 SI, 04SI, 06SI, 07SI and 08SI all show a significant amount of proteobacteria (0.5 to 17%). These data suggest that oxycodone can alter the composition of the small intestine microbiome dramatically (2/7) and give yield to pathogenic populations such as proteobacteria (5/7).
As can be derived from the above table, no completely altered composition was observed upon administration of the oxycodone/naloxone combination. Further, no pathogenic populations such as proteobacteria were detected in the mice treated with the oxycodone/naloxone combination.
Analysis of the Colon
The contents of the colon of the different groups were obtained as described above. The presence and the amount of bacteria of different phyla was then determined in the control [untreated] (G1), the vehicle-treated (G3), the oxycodone-treated (G6) and in the oxycodone/naloxone-treated (G7) groups according to standard methods. The results are shown in
An increase in proteobacteria in the G6-group was observed compared to the remaining groups. The addition of naloxone thus reverses the effect on the microbiome in the colon induced by oxycodone.
Analysis of the Mucosal Scraping of the Jejunum of the Small Intestine: TLR2-Expression
The mucosal scraping of the jejunum was obtained as described above and the expression level of the TLR2-mRNA was determined by a quantitative RT-PCR according to standard methods using β-actin mRNA as normalization control.
Clearly, TLR2-expression is upregulated in the jejunum in the oxycodone-treated mice, whereas the level of TLR2 is back to normal in the oxycodone/naloxone-treated mice. Naloxone is thus preventing an oxycodone-induced TLR2 upregulation. As can inter alia be derived from the publication by Meng et al., supra, a TLR2 upregulation is supposed to be involved in mucosal barrier defects resulting in bacterial translocation.
An exploratory, double-blind, double-dummy, randomized, 2-period, crossover, Phase IIa study to assess the influence of oxycodone/naloxone prolonged release tablets (OXN PR) compared to oxycodone prolonged release tablets (OxyPR) on intestinal microbiota and other gastrointestinal (GI) parameters in subjects suffering from non-malignant pain requiring an equivalent of 20 to 50 mg oxycodone PR per day.
The main goal of this example resides in the comparison of several GI parameters in patients suffering from pain and constipation and being either treated with oxycodone or oxycodone/naloxone. Patients suffering from pain and opioid-induced constipation were chosen since it appears likely that other GI parameters apart from constipation (e.g. the microbiota) may also be altered in these patients and that a comparison of the effects of oxycodone and of oxycodone/naloxone on such other GI parameters may also be carried out and allow an analysis of the potential reversibility if a combination of oxycodone and naloxone is administered.
Objectives of main interest:
This study is a multi-centre, exploratory, double-blind, double-dummy, randomized, 2-period, cross-over, Phase IIa study in subjects with severe non-malignant pain requiring a WHO step II/III opioid therapy in a daily dose of 20-50 mg oxycodone PR at randomization. During the Run-in Period subjects prestudy opioid treatment will be terminated and switched to oxycodone PR, which will be titrated to an effective analgesic dose between 20-50 mg/day of OxyPR. Oxycodone immediate release (OxyIR) is permitted as analgesic rescue medication during the study up to a maximum of 6 dosages per day. From Visit 2 (start of Run-in Period) onwards subjects will be allowed to take bisacodyl suppository only as rescue medication for constipation. Subjects will be randomized in a 1:1 ratio to two treatment groups and will receive study medication (either OXN PR or OxyPR). The starting dose is the OxyPR dose the subjects received at the end of the Run-in Period. The Double-blind Phase consists of 2 Periods of 24 days (Period 1: 24 days; Period 2: 24 days) and during each Period subjects will receive study medication. Subjects receiving OXN PR during the first Period will receive OxyPR in the subsequent Period and subjects receiving OxyPR during the first Period will receive OXN PR during the second one. During the Double-blind Phase no titration of the study medication dose is permitted. At the Follow-up Visit (AE-FU), which can be performed as an investigational site visit or telephone visit, safety assessment will be performed.
Study Design: See
Number of Subjects: The planned total number is 80 evaluable subjects. With respect to an assumed dropout rate of 20% of subjects, approximately 100 subjects will be randomized in total, and about 120-130 subjects will be screened.
Indication and Criteria for Inclusion/Exclusion:
Inclusion Criteria:
Reference Treatment, Dose, and Mode of Administration:
During the Run-in Period dosing is fixed and symmetrical (20, 30, 40 and 50 mg/day OxyPR). The OxyPR dose should be titrated until an effective analgesic dose has been established.
During the Double-blind Phase dosing is fixed and symmetrical (20, 30, 40 and 50 mg/day OxyPR for subjects receiving OxyPR and 20/10, 30/15, 40/20 and 50/25 mg/day for subjects receiving OXN PR). Subjects will start the Double-blind Phase with the OxyPR dose, which they received at the end of the Run-in Period.
Concomitant Medication Including Rescue:
All other medications not prohibited by the protocol and considered necessary for the subject's welfare may be administered and/or continued under the supervision of the investigator.
Duration of Treatment and Study Duration:
Pre-randomization Phase:
Double-blind Phase:
AE Follow-up Period: 7 Days
Total Duration: Up to approximately 97 days
Treatment Schedule (Procedure):
Pre-randomization Phase (up to 42 days):
Screening (Up to 14 Days): At Visit 1, after written informed consent is obtained, subjects will undergo complete evaluation for eligibility. Subjects meeting the predefined assessment criteria (inclusion/exclusion) may continue the study. A blood sample for genetic analysis will be drawn at Visit 3 from those subjects who voluntarily provide a separate informed consent. Subjects will stay with their prestudy medication until Visit 2.
Run-in Period (7 to 28 Days): At Visit 2, subjects will have their opioid therapy converted to open-label OxyPR, which will be titrated to an effective analgesic dose between 20-50 mg/day of OxyPR. OxyIR will be available as analgesic rescue medication. Subjects will also have their prestudy laxative therapy converted to the study laxative (bisacodyl suppository) to be used per the study routine for constipation during this period (no sooner than 72 hours after their most recent BM as rescue medication for constipation). The 7-day baseline assessment in the Run-In Period will start no sooner than the day of the initial dose conversion to OxyPR.
Double-blind Phase (7 Weeks):
Subjects will be randomised at Visit 3 to OXN PR or OxyPR in a 1:1 ratio. Subjects will start the Double-blind Phase at the same dose of OxyPR that they received at the end of the Run-in Period. Subjects will receive during Period 1 either OXN PR or OxyPR. After approximately 3.5 weeks of treatment subjects will enter Period 2 of the Double-blind Phase, in which the treatment will be switched. Subjects receiving OXN PR in Period 1 will receive OxyPR in Period 2, while Subjects receiving OxyPR in Period 1 will receive OXN PR in Period 2. Double-blind study medication will be administered in a double-dummy manner. Subjects will be permitted to take OxyIR as analgesic rescue; it may be dosed every 4 hours as needed.
Titration of the study medication dose is not permitted during the Double-blind Phase. During the Double-blind Phase subjects will follow the laxative regimen.
Other laxatives, except for regular natural dietary fibre supplementation, will not be permitted. During each crossover period the subject will attend 4 investigational site visits and 2 telephone visits. The subjects will attend the investigational site visits at a pain management clinic 7 (Visit 6 and 12), 14 (Visit 7 and 13) and 24 (Visit 9 and 15) days following the start of each period. Furthermore, 21 days (Visit 8 and 14) following the start of each period the subject will attend a visit at the gastroenterologist site.
Safety Follow-up (7 days): Subjects will be followed up for safety 7 days after receiving the last dose of study medication.
General Guidance for Breath Test:
Enrolled Population—The enrolled population is defined as all subjects who signed informed consent;
Full Analysis Population—The full analysis population is defined as all randomized subjects who receive at least one dose of IMP and have at least one post-baseline endpoint;
Run-in Period Safety Population—The safety population is defined as all subjects who receive at least one dose of study medication in Run-in Period;
Double-blind Safety Population—The safety population is defined as all randomized subjects who receive at least one dose of IMP in Double-blind Phase.
Parameters of Main Interest:
Intestinal Microbiota Analysis: For each subject stool samples will be collected during the week prior to randomization, between Visit 7 and 8 during Period 1, and between Visit 13 and 14 during Period 2. The effect of OXN PR and OxyPR on intestinal microbiota will be explored. 16S rRNA based deep-sequencing technique will be used for the quantitative gene expression analysis to examine the diversity of gut microbiota targeting specific bacterial phylogenetic groups (phylum-level classification) and selected species (genus or species-level classification). Analyses will be performed for the following bacterial groups/individual bacteria: Bacteroides (B. vulgates or B. fragilis), Bifidobacteria, Enterococci, Escherichia coli, Lactobacilli, Clostridia (C. perfringes, C. difficile) and Eubacteria.
Combined Measurement of Orocaecal Transit Time and Gastric Emptying:
Lactulose—H2 breath test: Lactulose is a synthetic disaccharide which cannot be hydrolyzed and absorbed in human small intestine. It is fermented by the colonic bacterial flora producing acids, water and gases (H2, CH4, CO2 etc.). Appearance of H2 (or CH4) in alveolar gas (expired air) after ingestion of lactulose reflects that lactulose has reached the cecum and has been fermented by the colonic anaerobic bacteria. Thus, the lactulose-H2-breath test is used as a marker/measure of orocecal transit time. Early ascent of H2 in alveolar gas indicates accelerated orocecal transit usually associated with increased small bowel motility. However, it can also be the result of small intestinal bacterial overgrowth (SIBO). Retarded increase in H2 concentration in the alveolar gas usually indicates decreased small intestinal motility resulting in prolonged orocaecal transit time.
CH4-breath test (based on lactulose—H2 breath test): CH4 is produced by methanogenic colonic flora instead of H2 producing bacteria in colon. Therefore measurement of CH4 along with H2 concentration in alveolar air will enhance the accuracy and reliability of lactulose—H2 breath test. CH4 appears to slow down intestinal transit time and its production is associated with constipation as symptom.
13C-acetate breath test (gastric emptying of liquids): Once 13C-acetate passes from the stomach, it is absorbed in the duodenum and metabolized in the liver forming 13C-carbon dioxide (13CO2) which is exhaled rapidly. Appearance of 13C in breath CO2 reflects the rate of gastric emptying of liquid and semi solid food.
To determine the effect of OXN PR and OxyPR on gastric emptying and orocecal transit time a combined breath test with lactulose and 13C-acetate will be performed at investigational site visits (Visit 8 and 14) at gastroenterologist's clinic. Following an overnight fast, breath samples will be collected before and after the ingestion of a solution containing 10 g lactulose, 150 mg 13C-acetate and 15 g glucose in 200 ml water. The time of a predefined increase in breath H2-concentration will serve as marker of orocecal transit time. In patients who do not exhale H2 (2-5% of population), CH4 exhalation will serve to estimate orocecal transit time. Based on the kinetics of appearance of 13C in breath CO2, rate of gastric emptying will be estimated. Moreover, small bowel transit time will be calculated by subtracting gastric emptying time from orocecal transit time.
Further Parameters:
Intestinal Metabolomics: For each subject stool samples will be collected during the week prior to randomization, between Visit 7 and 8 during Period 1, and between Visit 13 and 14 during Period 2 (same stool samples will be used as for microbiota analyses). The effect of OXN PR and OxyPR on intestinal metabolome will be explored. Metabolomic technology will be used to assess the biochemical composition of intestine based on metabolite assessment and mapping of respective compounds to corresponding metabolic pathways.
Serum Metabolomics: For each subject blood samples will be collected at Visit 1, 9 and 15. The effect of OXN PR and OxyPR on serum metabolome will be explored. Metabolomic technology will be used to assess the biochemical composition of the serum based on metabolite assessment and mapping of respective compounds to corresponding metabolic pathways.
Abdominal Girth: Abdominal girth of each patient will be measured before and 2 hours after the ingestion of test meal at Visit 8 and Visit 14. Any change in the buildup of intestinal gas, abdominal distension and bloating in subjects receiving OXN PR or Oxy PR will be determined. Abdominal girth will be measured as distance around the abdomen at the level of navel (belly button).
Stool Consistency: Stool consistency will be assessed at randomization (Visit 3), and end of Period 1 (Visit 9) and Period 2 (Visit 15) of Double-blind Phase.
Subjective Assessment of Constipation: This will be measured by BFI, a validated scale for the assessment of opioid-induced constipation. BFI will be measured at Screening (Visit 1), start of Run-in Period (visit 2), randomization (Visit 3), and Visit 6, 7, 9, 12, 13 and 15. BFI will be the mean of the following items (assessed at each visit): Ease of defecation (numerical analogue scale [NAS], 0=easy/no difficulty; 100=severe difficulty), Feeling of incomplete bowel evacuation (NAS, 0=not at all, 100=very strong), Personal judgment of constipation (NAS, 0=not at all, 100=very strong).
DoloTest®: DoloTest® is a validated visual health related (HR) QoL measurement tool used in pain patients providing subjective pain assessment and its impact on QoL. The test is composed of 8 domains represented by 8 Visual Analogue Scale (VAS) lines arranged in a radar plot. The radar plot shape of the test provides a graphical presentation of the test called DoloTest® Profile. The VAS lines are used to score the corresponding domains including pain. Addition of each scored domain provides a sum score called DoloTest® Score. To compare the impact of pain on QoL in subjects treated with OXN PR compared to those treated with Oxy PR, DoloTest® will be conducted at Screening (Visit 1), randomization (Visit 3), and end of Period 1 (Visit 9) and Period 2 (Visit 15) of Double-blind Phase.
Intestinal Microbiota and GI Parameters (Breath Tests) Correlation: The results of intestinal microbiota analysis will be correlated with the results of breath tests in an exploratory manner. The result of OXN PR and OxyPR treatments will be compared.
Intestinal Microbiota and BFI Correlation: The results of intestinal microbiota analysis will be correlated with the results of BFI in an exploratory manner. The result of OXN PR and OxyPR treatments will be compared.
Intestinal Microbiota and Metabolome Correlation: The results of intestinal microbiota analysis will be correlated with the results of intestinal metabolome analysis in an exploratory manner. The result of OXN PR and OxyPR treatments will be compared.
Immune and Inflammatory Response Parameters (Microbiota Correlation): For each subject blood samples will be collected at Screening (Visit 1), Visit 9 and Visit 15. To compare the effect of OXN PR with OxyPR serum level of following parameters will be estimated: TNFα (acts as inflammatory mediator in acute-phase, produced by macrophages), CRP (a classical acute-phase protein synthesized by the liver in response to factors released by fat cells), IL-6 (acute-phase cytokine produced by T cells and macrophages), LPS (plasma endotoxin and major component of the cell wall of gram-negative bacteria), LBP (acute-phase protein produced mainly by hepatocytes), sCD14 (CD14 exists in two forms, a membrane fixed CD14 (mCD14) glycophosphatidylinosital anchored protein also found on the surface of human intestinal epithelial cell lines (Funda D P, 2001) and a soluble form (sCD14). mCD14 acts as a receptor for LPS (endotoxin)-LBP (septin)-complex and the presence of LPS in blood increases synthesis of mCD14 in that region. Apart from protease-mediated shedding from leucocytes, sCD14 is also produced by hepatocytes (Matsuura K 1994; Fearns C, 1995; Liu S, 1998; Su G L, 1999; Pan Z, 2000; Bas S, 2004), which represents the major source of acute-phase protein (Baumann H, 1994). Synthesis of sCD 14 in the liver is regulated by IL-6 (Dinarello C A, 1984; Baumann H, 1987), IL-1β (Dinarello C A, 1984; Baumann H, 1990), TNFα (Perlmutter D H, 1986), and glucocorticoids (dexamethasone) (Baumann H, 1987; Gabay C, 1999). sCD 14 can interact directly with T and B cells (Arias M A, 2000; Rey Nores J E, 1999) leading to immune and/or inflammatory response. [LPS, LBP and sCD14 are described as ‘signs of endotoxin-signaling cascade activation’], GLP-2 (GLP-2 is secreted by enteroendocrine cells in a nutrient dependent-manner (Orskov C, 1987; Brubaker P L, 1997). It is trophic to the intestinal mucosa, reduces epithelial permeability, and decreases meal-stimulated gastric acid secretion and gastrointestinal motility (Drucker D J, 2002, online 2007)).
Immune and Inflammatory Response Parameters and GI Parameters (Breath Tests) Correlation: There is evidence that gastric emptying is impaired in patients with inflammatory bowel disease and diverticulitis (Keller J, 2009). The results of immune and inflammatory parameters will be correlated with the results of breath tests in an exploratory manner. The result of OXN PR and OxyPR treatments will be compared.
Safety Assessments: Safety will be assessed by documentation of adverse events (AEs), clinical laboratory results, vital signs, physical examinations, electrocardiograms (ECGs).
Statistical Methods:
Efficacy Analyses: All parameters will be analyzed in a descriptive/exploratory manner. Statistics including 95% CI by treatment will be provided. At least for the parameters of main interest an ANCOVA with treatment, period and/or sequence factors will also be performed.
Safety Analyses: The number and percentage of subjects reporting AEs will be summarized by treatment group. In addition, AEs by severity, AEs by relationship to study medication, AEs leading to discontinuation from the study, and serious AEs will be summarized. AE rates in relation to study day, e.g. cumulative incidence, will also be summarized. Clinical laboratory parameters and vital signs will be summarized descriptively. The frequency of laboratory and vital signs results with respect to normal ranges will also be presented.
Sample Size Rationale:
The sample size of 80 evaluable subjects was not statistically estimated as this study serves as an exploratory hypothesis generating study, but this sample size is considered as providing sufficient evidence from clinical point of view.
| Number | Date | Country | Kind |
|---|---|---|---|
| 13177646 | Jul 2013 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2014/065816 | 7/23/2014 | WO | 00 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2015/011189 | 1/29/2015 | WO | A |
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| Number | Date | Country | |
|---|---|---|---|
| 20160184293 A1 | Jun 2016 | US |
