Patent Application
20210052703
The present disclosure relates to the use of various doses of an aqueous parenteral pharmaceutical composition containing Glucagon-like peptide 1 (GLP-1) for treating obesity, weight management, and other conditions.
GLP-1 is an insulinotropic peptide acting on GLP-1 receptor distributed through the whole body, and particularly on pancreatic insulin-secreting β cells. This type of hormones can promote insulin secretion, and also stimulates insulin signaling independently, resulting a glucose hypoglycemic effect. Instability of GLP-1 includes two general aspects, i.e., physical and chemical aspects. Physical instability includes, for example, denaturation, surface adsorption, aggregation, precipitation, gelatination, and the like, and chemical instability includes, for example, hydrolysis, deamination, oxidization, racemization, isomerization, β-elimination, disulfide bond exchange, and the like. Instability not only shortens the shelf life but also affects the efficacy of GLP-1 compositions. To solve the instability problem, either nanoparticles are used to deliver GLP-1 or GLP-1 is modified to improve stability. However, nanoparticle delivery increases the production cost and formulation complexity, and modification of GLP-1 is often associated with increased toxicity. See Lee, Basic Clin. Pharmacol. Toxicol. 118(3): 173-180 (2016).
Accordingly, a composition containing GLP-1 in its natural, unmodified form with increased stability and improved efficacy at a low dose is highly desirable. The technology and methods disclosed herein satisfy this need in the art.
In one aspect, the present disclosure provides a method of treating obesity or overweight by administering to a subject suffering from obesity or overweight a therapeutically effective amount of a composition comprising a GLP-1 peptide (e.g., GLP-1 (7-36), GLP-1 (7-36)NH2, GLP-1 (7-35), or GLP-1 (7-37)), the therapeutically effective amount of the GLP-1 peptide is from about 10 μg/kg to about 60 μg/kg body weight, or about 0.11 mg/day to about 0.66 mg/day (e.g., in a human subject). In some embodiments, the GLP-1 peptide is a recombinant human GLP-1 peptide. In some embodiments, the GLP-1 peptide is a chemically synthesized GLP-1 peptide. In some embodiments, the composition comprising a GLP-1 peptide (the GLP-1 composition) is administered by parenteral injection. In some embodiments, the GLP-1 composition is administered by intravenous injection, intramuscular injection, or subcutaneous injection. In some embodiments, the GLP-1 composition is administered for an extended period of time, up to 1 year, up to 2 years, up to 3 years, up to 4 years, up to 5 years, up to 6 years, up to 7 years, up to 8 years, up to 9 years, up to 10 years, up to 11 years, up to 12 years, up to 13 years, up to 14 years, up to 15 years, up to 16 years, up to 17 years, up to 18 years, up to 19 years, up to 20 years, up to 21 years, up to 22 years, up to 23 years, up to 24 years, up to 25 years, up to 26 years, up to 27 years, up to 28 years, up to 29 years, up to 30 years, or up to 31 years by continuous or periodic administration.
In some embodiments, the therapeutically effective amount of the GLP-1 composition for treating obesity or overweight in a female subject is lower than that in a male subject. In some embodiments, the therapeutically effective amount of the GLP-1 for treating obesity or overweight in a female subject is at least 10%, at least 20%, at least 30%, at least 40%, at least 50%, at least 60%, or at least 70% lower than that for treating obesity or overweight in a male subject to achieve the same or similar therapeutic effects. In some embodiments, the therapeutically effective amount of the GLP-1 for treating obesity or overweight in a female subject is from about 10 μg/kg to about 60 μg/kg body weight, or about 0.11 mg/day to about 0.66 mg/day (e.g., in human subjects). In some embodiments, the therapeutically effective amount of the GLP-1 for treating obesity or overweight in a male subject is from about 30 μg/kg to about 60 μg/kg body weight, about 0.33 mg/day to about 0.66 mg/day (e.g., in human subjects).
In another aspect, the disclosure relates to a method of managing body weight by administering to a subject in need thereof a therapeutically effective amount of a composition comprising GLP-1 (7-36) or GLP-1 (7-36)NH2, preferably a recombinant human GLP-1 (7-36) or GLP-1 (7-36)NH2, the therapeutically effective amount of the GLP-1 composition is from about 10 μg/kg to about 60 μg/kg body weight, or about 0.11 mg/day to about 0.66 mg/day (e.g., in a human subject). In some embodiments, the GLP-1 peptide is a chemically synthesized GLP-1 peptide. In some embodiments, the GLP-1 composition is administered by parenteral injection. In some embodiments, the GLP-1 composition is administered by intravenous injection, intramuscular injection, or subcutaneous injection. In some embodiments, the GLP-1 composition is administered for an extended period of time, up to 1 year, up to 2 years, up to 3 years, up to 4 years, up to 5 years, up to 6 years, up to 7 years, up to 8 years, up to 9 years, up to 10 years, up to 11 years, up to 12 years, up to 13 years, up to 14 years, up to 15 years, up to 16 years, up to 17 years, up to 18 years, up to 19 years, up to 20 years, up to 21 years, up to 22 years, up to 23 years, up to 24 years, up to 25 years, up to 26 years, up to 27 years, up to 28 years, up to 29 years, up to 30 years, or up to 31 years by continuous or periodic administration. In some embodiments, the body weight loss of the subject the GLP-1 composition is less than 100%, less than 95%, less than 90%, less than 85%, less than 80%, or less than 75% of the body weight loss of the subject receiving the GLP-1 composition. In some embodiments, the therapeutically effective amount of the GLP-1 for weight management in a female subject is from about 10 μg/kg to about 60 μg/kg body weight, or about 0.11 mg/day to about 0.66 mg/day. In some embodiments, the therapeutically effective amount of the GLP-1 for weight management in a male subject is from about 30 μg/kg to about 60 μg/kg body weight, or about 0.33 mg/day to about 0.66 mg/day.
Surprisingly, at a significantly lower dose, the GLP-1 composition described herein achieves pharmacokinetics significantly different from the liraglutide composition in treating overweight and obesity. Additionally, the therapeutically effective amount of the GLP-1 composition for a female subject is significantly lower than the therapeutically effective amount of the GLP-1 composition for a male subject to achieve the same or similar therapeutic effects.
The World Health Organization (WHO) has listed obesity as a disease since 1948. The worldwide occurrence of obesity has more than doubled since 1980. Ng et al., Lancet. 384: 766-781 (2014). Overweight or obesity is described as an abnormal or overly accumulation of body fat due to long-term energy intake exceeding energy expenditure. Overweight and obesity are significant risk factors for non-contagious diseases such as cardiovascular diseases, type 2 diabetes (T2DM), skeletal muscle abnormalities, and certain cancers. Van Bloemendaal et al., J. Endocrinol. 221: T1-T16 (2014). These diseases and conditions associated with overweight or obesity place a significant financial burden on public healthcare.
The native form of GLP-1 is secreted by intestinal L-cells after a meal, and is a strong peptide stimulator of insulin secretion. GLP-1 is a potential therapy for type 2 diabetes. Holst, Physiol. Rev. 87: 1409-1439 (2007). GLP-1 has two active forms, GLP-1 (7-36)-NH2 and GLP-1 (7-37). Upon entry into circulation, GLP-1 is rapidly degraded by dipeptidyl peptidase-4 (DPP4), resulting in a short half-life of about 2 minutes. Kieffer et al., Endocrinology 136: 3585-3596 (1995). Besides its effect on controlling blood sugar, GLP-1 and its analogs were found to have effects on inducing body weight loss, slowing stomach emptying, and increasing satiety. Monami et al., Exp. Diabetes Res. 2012: 672658 (2012). FDA approved Saxenda (liraglutide 3 mg) in December 2014, which is the first NDA application for GLP-1 analogs, and which is a long-term weight management supplemented with low-calorie diet and increase of physical activity for obesity adults having at least one disease or condition associated with overweight, such as type 2 obesity.
In the context of this disclosure, the phrase a “therapeutically effective amount” or an “effective amount” of a pharmaceutical composition comprising GLP-1 as used herein is an amount of the pharmaceutical composition that produces a desired therapeutic effect in a subject, such as treating obesity or overweight, weight management, inducing weight loss, etc. In certain embodiments, the therapeutically effective amount is an amount of the pharmaceutical composition that yields maximum therapeutic effect. In other embodiments, the therapeutically effective amount yields a therapeutic effect that is less than the maximum therapeutic effect. For example, a therapeutically effective amount may be an amount that produces a therapeutic effect while avoiding one or more side effects associated with a dosage that yields maximum therapeutic effect. In some embodiments, a therapeutically effective amount is the minimal amount that produces a therapeutic effect. A therapeutically effective amount for a particular composition will vary based on a variety of factors, including but not limited to the characteristics of the therapeutic composition (e.g., activity, pharmacokinetics, pharmacodynamics, and bioavailability), the physiological condition of the subject (e.g., age, body weight, sex, disease type and stage, medical history, general physical condition, responsiveness to a given dosage, and other present medications), the nature of any pharmaceutically acceptable carriers, excipients, and preservatives in the composition, and the route of administration. One skilled in the clinical and pharmacological art will be able to determine a therapeutically effective amount through routine experimentation, namely by monitoring a subject's response to administration of the pharmaceutical composition and adjusting the dosage accordingly. For additional guidance, see, e.g., Remington: The Science and Practice of Pharmacy, 22nd Edition, Pharmaceutical Press, London, 2012, and Goodman & Gilman's The Pharmacological Basis of Therapeutics, 12th Edition, McGraw-Hill, New York, N.Y., 2011, the entire disclosures of which are incorporated by reference herein.
In some embodiments, a therapeutically effective amount of a pharmaceutical composition comprising GLP-1 disclosed herein is in the range from about 10 μg/kg to about 60 μg/kg body weight of the active ingredient, GLP-1, or from about 0.11 mg/day to about 0.66 mg/day of GLP-1 (e.g., in a human subject). In some embodiments, a therapeutically effective amount of a pharmaceutical composition comprising GLP-1 disclosed herein for a male subject is from about 30 μg/kg to about 60 μg/kg body weight of the active ingredient, GLP-1, or from about 0.33 mg/day to about 0.66 mg/day of GLP-1 (e.g., in a human subject). In some embodiments, a therapeutically effective amount of a pharmaceutical composition comprising GLP-1 disclosed herein for a female subject is from about 10 μg/kg to about 60 μg/kg body weight of the active ingredient, GLP-1, or from about 0.11 mg/day to about 0.66 mg/day of GLP-1 (e.g., in a human subject).
The terms “treat,” “treating,” and “treatment” as used herein with regard to a condition refers to alleviating the condition partially or entirely, preventing the condition, decreasing the likelihood of occurrence or recurrence of the condition, slowing the progression or development of the condition, or eliminating, reducing, or slowing the development of one or more symptoms associated with the condition.
As used herein, the term “subject” refers to a mammalian subject, preferably human. A “subject in need thereof” refers to a subject who has been diagnosed with obesity or overweight, who is at a risk of weight gain, or who desires to control weight gain or induce weight loss. The phrases “subject” and “patient” can be used interchangeably herein.
As used herein, the term “comprising” with regard to a composition or method means that the composition or method includes at least the recited elements. The term “consisting essentially of” means that the composition or method includes the recited elements, and may further include one or more additional elements that do not materially affect the novel and basic characteristics of the composition or method. For example, a composition consisting essentially of recited elements may include those recited elements plus one or more trace contaminants from the isolation and purification method, pharmaceutically acceptable carriers such as phosphate buffered saline, preservatives, and the like. The term “consisting of” means the composition or method includes only the recited elements. Embodiments defined by each of the transitional terms are within the scope of this invention.
In some embodiments, the GLP-1 composition disclosed herein comprises a recombinant human GLP-1 (7-36) peptide having the sequence of: His-Ala-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Val-Ser-Ser-Tyr-Leu-Glu-Gly-Gln-Ala-Ala-Lys-Glu-Phe-Ile-Ala-Trp-Leu-Val-Lys-Gly-Arg (SEQ ID NO: 1), e.g., referred to as Beinaglutide in this disclosure. Beinaglutide has a molecular formula of C149H225N39O46, and a molecular weight of 3298.7. This peptide is essentially the same as the active form of circulating GLP-1 except for the endogenous amidation, where NH2 in the natural form is replaced by OH group in the recombinant peptide. Beinaglutide includes a C-terminal free carboxyl group, similar to glycine-extended GLP-1 (7-37). In other embodiments, GLP-1 (7-35) or GLP-1 (7-37) can be used in the disclosed technology. The sequences of GLP-1 (7-35) and GLP-1 (7-37) are as follows: His-Ala-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Val-Ser-Ser-Tyr-Leu-Glu-Gly-Gln-Ala-Ala-Lys-Glu-Phe-Ile-Ala-Trp-Leu-Val-Lys-Gly (SEQ ID NO: 2), and His-Ala-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Val-Ser-Ser-Tyr-Leu-Glu-Gly-Gln-Ala-Ala-Lys-Glu-Phe-Ile-Ala-Trp-Leu-Val-Lys-Gly-Arg-Gly (SEQ ID NO: 3).
In clinical pharmacokinetic studies using monkey models, Beinaglutide demonstrated a half-life of about 15-30 minutes when administered subcutaneously. In clinical trial phase III in China for treating diabetes, 346 diabetes patients who received Beinaglutide (0.2 mg, TID) for 12 weeks demonstrated significant body weight loss as well as a decrease of glycated hemoglobin level in the blood, compared to a control group of 113 patients. The most common side effects for these patients were nausea and vomiting, however, these side effects were temporary and not worse than other similar GLP-1 analog therapies.
Beinaglutide can be isolated after expression in E. coli, and subsequently formulated into an injectable formulation. In the pharmaceutical composition of the present disclosure, the GLP-1 peptide has a concentration of about 0.1 to about 20 mg/mL, about 0.2 to about 10 mg/mL, about 0.05 to about 0.5 mg/mL, about 0.5 to about 5 mg/mL, about 1 to about 5 mg/mL, or about 2 to about 4 mg/mL. Unless specifically defined otherwise, “about” refers to the difference from a stated numerical value in a range of ±10%. For example, in the formulation of the present disclosure, the GLP-1 concentration is up to 2 mg/m, and can be stored in dark for about 2 years at 2-8° C.
The pharmaceutical composition of the present disclosure has a pH value of about 3.5 to about 5.0, about 3.5 to about 4.5, about 3.6 to about 4.2, about 3.6 to about 4.1, about 3.6 to about 4.0, or about 3.6 to about 3.9. At this pH range, stability of the GLP-1 composition is improved, and the composition can be stored in dark for about 2 years or more at 2 to 8° C.
The GLP-1 composition disclosed herein may contain one or more buffer salt to maintain the desired pH range of the composition, including sodium acetate, acetic acid, etc. Additional ingredients for the GLP-1 composition may include one or more of a preservative (e.g., phenols and the like), an isotonic agent (e.g., mannitol, propylene glycol, and the like), and a dissolution enhancer (e.g., propylene glycol and the like).
In some embodiments, Beinaglutide can be administered to patients suffering from overweight or obesity by subcutaneous injection to reduce body weight. Other suitable injection routes can be used as well. The effects of Beinaglutide on controlling or reducing body weight are demonstrated by the working examples.
Prophylactic and/or Therapeutic Use of the GLP-1 Composition
The present disclosure provides use of the pharmaceutical composition comprising GLP-1 for treating or preventing various conditions, including obesity, bulimia, and/or overweight. This disclosure also relates to the use of the pharmaceutical composition comprising GLP-1 for weight management, slowing gastric emptying, and/or improving satiety.
According to the standard published by Centers for Disease Control and Prevention (CDC) and World Health Organization (WHO), a BMI below 18.5 indicates underweight, a BMI between 18.5 and 24.9 indicates normal or healthy weight, a BMI between 25.0 and 29.9 indicates overweight, and a BMI at 30.0 or above indicates obesity.
Treatment of Obesity
In one aspect, provided herein is a method of treating obesity comprising administering to the subject a therapeutically effective amount of the pharmaceutical composition comprising GLP-1, the therapeutically effective amount is in the range from about 10 μg/kg to about 60 μg/kg body weight of the active ingredient, GLP-1, or from about 0.11 mg/day to about 0.66 mg/day of GLP-1 (e.g., in a human subject).
Treatment of Bulimia
In one aspect, provided herein is a method of treating bulimia comprising administering to the subject a therapeutically effective amount of the pharmaceutical composition comprising GLP-1, the therapeutically effective amount is in the range from about 10 μg/kg to about 60 μg/kg body weight of the active ingredient, GLP-1, or from about 0.11 mg/day to about 0.66 mg/day of GLP-1 (e.g., in a human subject).
Body Weight Management
In another aspect, provided herein is a method of managing body weight in a subject comprising administering to the subject a therapeutically effective amount of the pharmaceutical composition comprising GLP-1 such that the body mass index (BMI) is decreased by at least 0.5%, at least 1%, at least 2%, or at least 3%, the therapeutically effective amount is in the range from about 10 μg/kg to about 60 μg/kg body weight of the active ingredient, GLP-1, or from about 0.11 mg/day to about 0.66 mg/day of GLP-1 (e.g., in a human subject). Alternatively, provided herein is a method of managing body weight in a subject comprising administering to the subject a therapeutically effective amount of the pharmaceutical composition comprising GLP-1 such that the body weight is decreased by at least 2%, at least 5%, at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, or at least 50%, the therapeutically effective amount is in the range from about 10 μg/kg to about 60 μg/kg body weight of the active ingredient, GLP-1, or from about 0.11 mg/day to about 0.66 mg/day of GLP-1 (e.g., in a human subject).
In some embodiments, body weight management includes inducing weight loss. In some embodiments, the body weight of the subject receiving the GLP-1 composition is less than 100%, less than 95%, less than 90%, less than 85%, less than 80%, less than 75% of the body weight of the subject who does not receive the GLP-1 composition.
Slowing Gastric Emptying
In another aspect, provided herein is a method of slowing gastric emptying comprising administering to the subject a therapeutically effective amount of the pharmaceutical composition comprising GLP-1, the therapeutically effective amount is in the range from about 10 μg/kg to about 60 μg/kg body weight of the active ingredient, GLP-1, or from about 0.11 mg/day to about 0.66 mg/day of GLP-1 (e.g., in a human subject).
Dosage of GLP-1
To achieve the same or a similar therapeutic effect for various conditions disclosed herein, the dosage of the GLP-1 composition is significantly lower than a pharmaceutical composition containing liraglutide. Additionally, the minimal dosage of GLP-1 to elicit a therapeutic effect in a female subject is significantly lower than the minimal dosage of GLP-1 to elicit the same or similar therapeutic effect in a male subject. In some embodiments, the minimal dosage of GLP-1 for a female subject is about 95%, about 90%, about 85%, about 80%, about 75%, about 70%, about 65%, about 60%, about 55%, about 50%, about 45%, about 40%, about 35%, about 30%, or about 25% of the minimal dosage of GLP-1 for a male subject to achieve the same or similar therapeutic effects. In general, a human dose is about 1/12 of the mouse dose, about ⅙ of the rat dose, or about ⅓ of the monkey dose. In some embodiments, provided herein is a product comprising a dose of 0.1 mg-0.4 mg once per day of GLP-1 peptide.
The following examples are provided to better illustrate the embodiments and are not to be interpreted as limiting the scope of any claimed embodiment. To the extent that specific materials are mentioned, it is merely for purposes of illustration and is not intended to limit the invention. One skilled in the art may develop equivalent means or reactants without the exercise of inventive capacity and without departing from the scope of the invention. It will be understood that many variations can be made in the procedures herein described while still remaining within the bounds of the present invention. It is the intention of the inventors that such variations are included within the scope of the invention.
This example demonstrates the effect of Beinaglutide injectable formulation on slowing stomach emptying. The Beinaglutide injectable formulation contains Beinaglutide of SEQ ID NO: 1 at 4.2 mg (42,000 U) in 2.1 ml.
Fifty 8-week old Sprague-Dawley (SD) rats having a body weight of between 248 g and 308 g (male) or between 184 g and 218 g (female) were on adaptive feeding for 7 days, weight of each taken, and then divided into 5 groups: buffer only control, low dose of Beinaglutide (15 μg/kg), medium dose of Beinaglutide (30 μg/kg), high dose of Beinaglutide (60 μg/kg), and liraglutide control (270 μg/kg). Each group had 10 rats, half male and half female. The tails of the rats were labeled as follows:
The dose selection is calculated based on human dose. The clinical human dose is estimated to be about 0.4 mg/injection, one injection per day, which corresponds to 36 μg/kg rat dose, calculated based on the body surface area. Accordingly, the rats were tested at a medium dose of 30 μg/kg, a low dose at 50% of the medium dose, and a high dose at 200% of the medium dose. The clinical human dose of liraglutide for treating obesity is 3.0 mg/injection, one injection per day, which corresponds to 270 μg/kg rat dose, calculated based on the body surface area.
Beinaglutide injectable formulation was provided by Shanghai Benemae Pharmaceutical Corporation (Benemae), which was a colorless, transparent liquid in 2.1 mL, containing 4.2 mg (42,000 U) of Beinaglutide. The Beinaglutide injectable formulation was stored in dark, at 2-8° C. The buffer only control is a clinical placebo of the Beinaglutide injectable formulation, also provided by Benemae as a colorless, transparent liquid and stored at 2-8° C. The positive control was liraglutide injectable formulation, which was stored in dark, sealed condition. The rats were raised and kept at the Laboratory Animal Center, Shanghai University of Traditional Chinese Medicine.
The injectable formulations were made and diluted at the time of experiment, as follows:
The rats were fasted for 16 hours with only water provided. Before being divided into groups, the rats were weighed and weights were recorded (cage numbering and tail labeling). Based on the body weight, the rats were randomly divided into 5 groups, 10 in each group, half male and half female. After grouping, the rats were labeled as shown in Table 1.
The rats were administered with appropriate amounts of Beinaglutide or liraglutide based on their body weights by subcutaneous injection. Female rats were injected after male rats, in the order of their group numbers: 101, 201, 301, 401, 501, 102, 202, 302, 402, 502, etc. The formulations were injected to the rats by lifting the skin in the back, placing the needle of the syringe subcutaneously and injecting. When retrieving the needle, the site of injection was pressed with hand to avoid leakage of the formulation. The amount of injection is about 0.1 ml/100 g body weight.
Five minutes after subcutaneous injection, gavage was conducted using 5% carbon powder suspension (in 2% carboxymethylcellulose solution) at 1.5 ml/100 g body weight. After 15 minutes, the rats were sacrificed, and the abdominal cavity was cut open, and cardia and pylorus of the stomach were ligatured immediately. The stomach was wiped dry with filter paper and weighed for the gross weight of the stomach. Then the content of the stomach was removed and the stomach was weighed for the net weight. The respective distance from the pyloric sphincter to the front of carbon powder suspension and to the distal end of the large intestine was measured.
As shown in Tables 3 and 4 and
This example demonstrates the activation effect of Beinaglutide on GLP-1 receptor signaling pathway.
GLP-1 receptor belongs to the family of G-protein coupled receptors and has seven transmembrane domains. The effects of Beinaglutide and the positive control GLP-1 (7-36)-NH2 on GLP-1 receptor were analyzed using CHO-K1 cells stably expressing GLP-1 receptor via a fluorescence detection of intracellular calcium levels. Beinaglutide induced intracellular calcium flow in the CHO-K1 cells in a concentration-dependent manner. Beinaglutide and the positive control GLP-1 (7-36)-NH2 exhibited similar EC50, at 118±48 and 141±18 nM, respectively. Both Beinaglutide and GLP-1 (7-36)-NH2 fully demonstrated activation effects on the GLP-1 receptor signaling pathway.
This example demonstrates the effect of Beinaglutide on blood sugar levels in animals in normal and diabetic animal models.
Beinaglutide was able to lower glucose-induced high blood sugar in mice and rabbits with normal glycemic index (GI), as well as to reduce the increase of blood sugar induced by alloxan and streptozotocin in mice and rats with normal GI, demonstrating its effects on lowering blood sugar. Animals having increased blood sugar had a normal GI, and when the blood sugar decreased, insulin level increased significantly and correlated with the decrease of blood sugar. However, in animals having a normal level of blood sugar, Beinaglutide neither decreased blood sugar nor increased blood insulin level, indicating that Beinaglutide promoted insulin secretion was dependent on the concentration of glucose.
This example demonstrates the effect of Beinaglutide on reducing body weight in diet-induced obesity cynomolgus monkeys.
Beinaglutide injectable formulation was subcutaneously administered to diet-induced obesity cynomolgus monkeys twice or three times a day, for a period of three weeks to evaluate the effects on decreasing appetite and body weight loss as well as the continuous effects and reversibility once the treatment was terminated.
Two male (10.5-11.5 kg) and two female (6.0-6.5 kg) obesity cynomolgus monkeys between 14-19 years old and having a BMI greater than 40 kg/m2 were used in this study. As shown in
The study included three periods: baseline period (the first week), treatment period (the second week through the seventh week), and recovering period (the eighth week). After the monkeys adapted to the meal time for at least 30 days, the body weight, BMI, and body composition of each animal was determined at day 7 of the first baseline period. These indexes were used as the baseline for evaluating the efficacy of Beinaglutide.
During the treatment period (second to seventh week), Group 1 monkeys were subcutaneously administered with blank control three times a day during week 2 through week 4, with Beinaglutide injectable formulation twice a day during week 5 through week 7. Group 2 monkeys were subcutaneously administered with Beinaglutide injectable formulation three times a day during week 2 through week 4, with blank control twice a day during week 5 through week 7. To improve tolerance of Beinaglutide and to determine the maximum tolerance dose for Beinaglutide, the dose of Beinaglutide was increased gradually during the study. Group 2 animals were administered three times a day at a dose of 10 μg/kg each time during week 2, three times a day at a dose of 20 μg/kg each time during week 3, and three times a day at a dose of 40 μg/kg each time during the first three days of week 4. Due to severe anorexia observed, the dose was reduced to 20 μg/kg each time during the remaining 4 days of week 4, shown in Table 6.
The dose for Group 1 animals during week 5 through week 7 was determined based on the dose given to Group 2 animals during week 2 through week 4. Group 1 animals were administered twice a day at a dose of 10 μg/kg each time during week 5, twice a day at a dose of 20 μg/kg each time during week 6, and twice a day at a dose of 20 μg/kg each time during week 7 (same dose as week 6). During the 6-week treatment period, the body weight and crown-rump height of each animal were measured at the end of each week. The body fat content was measured at week 4 and week 7. No administration was given during week 8.
During the eight weeks of this study, the amount of the food intake of each meal for each animal was recorded. The effects of Beinaglutide of Group 1 on affecting the food intake, body weight and BMI were evaluated by comparing to the baseline levels during week 4 and week 7. The effects of Beinaglutide of Group 2 on affecting the food intake, body weight and BMI were evaluated by comparing to the baseline levels during week 1 and week 4.
Beinaglutide was diluted 30 minutes prior to injection from 2 mg/ml to 0.2, 0.4, or 0.8 mg/ml for injection in a volume of 0.05 ml/kg. The animals were given three meals a day, including monkey feed in the morning (around 8:30) and in the afternoon (around 16:00) and fruits in between (around 14:00). Each animal was given 150 g monkey feed. After half an hour, if all monkey feed was consumed, the animal was given an extra 50 g of monkey feed. The animals were given about one hour to finish each meal and the leftover was weighed and recorded to calculate the food intake. Each animal was provided with the same calories of fruits, based on Table 7.
The body weight was measured once a week, and crown-rump height was measured at the end of week 1, week 4, and week 7 when Dual-Energy X-ray Absorptiometry (DEXA) scan was taken. The animals were anesthetized by intramuscular administration of 0.02 m/kg Shumianning. While resting on one side, the animals were measured from the top of the head to the bottom of tail as the crown-rump height. BMI was calculated using the formula: BMI=body weight (kg)/crown-rump height (m){circumflex over ( )}2. DEXA scan was conducted while the animals were anesthetized and body compositions were analyzed based on DEXA scan.
During the study, the animals were observed for at least three times a day before and during feeding for any abnormal behavior, or signs of pain or tension. After being administered with Beinaglutide or blank control, the animals were observed for any of the following symptoms, including loss of appetite, sleepiness, diarrhea, constipation, indifference, vomiting, inflammation or any other conditions around the injecting area. If symptoms of low blood sugar, such as shivering or coma, were observed, the blood glucose test was given to the animals to confirm low blood sugar and the animals were given conservative treatment.
The daily food intake for each animal was monitored during the entire study period. As shown in
The calories intake for each animal was calculated based on the food intake and the values before, during and after treatment with Beinaglutide were compared, as shown in
Accordingly, two or three subcutaneous injections of Beinaglutide per day significantly reduced food intake in both male and female obesity monkeys. In fact, Group 2 animals showed severe signs of anorexia when administered with a dose of 40 μg/kg Beinaglutide in the first three days of week 4, and therefore, the dose had to decrease to 20 μg/kg during the remaining days of week 4. It was estimated that the maximum tolerance dose of Beinaglutide for diet induced obesity cynomolgus monkeys was three times a day, 20-40 μg/kg each time.
During the entire study period, each monkey was weighed on a weekly basis and all body weigh information was recorded in Table 8.
The male and female animals in Group 1 did not show any substantial change in body weight during week 2 through week 4 while blank control was administered; in contrast, the monkeys in Group 2 showed continuous weight loss since Beinaglutide was administered, as shown in
Crown to rump height of each animal was measured by the end of week 1, week 4, and week 7, and BMI was calculated based on the body weight and crown to rump height. BMI decreased in the two groups of animals after three weeks of Beinaglutide treatment.
DEXA scan was performed on each animal at week 1, week 4, and the end of week 7 and information about body composition is shown in Table 9.
At the end of week 4, Group 1 animals which were administered with blank control had a slight increase in body fat content compared to the baseline level, however, Group 2 animals which were administered with Beinaglutide had a significant decrease in body fat content. At the end of week 7, Group 1 animals which were administered with Beinaglutide also had a decrease in body fat content compared to the baseline level. The body fat percentage was calculated based on the percentage of body fat in total body weight.
In trial 5A, Beinaglutide (four dose groups of 0 mg, 0.1 mg, 0.15 mg, and 0.2 mg, three times a day, 0 mg, 0.1 mg, 0.15 mg or 0.2 mg each time) and/or glipizide (glipizide controlled release tablets (Rui Yining), 5 mg once a day orally) was administered to type 2 diabetic patients (96 patients) with poor glycemic control of sulfonylureas (e.g., glipizide). To observe the changes in body weight and BMI, and adverse reactions such as gastrointestinal reactions in the subjects treated with Beinaglutide and glipizide alone or in combination at different doses.
The drug of choice for the treatment of diabetes is metformin. In trial 5B, Beinaglutide (0 mg, 0.1 mg, 0.15 mg, and 0.2 mg in four dose groups, three times a day, 0 mg, 0.1 mg, 0.15 mg or 0.2 mg each time) and metformin (oral monotherapy, therapeutic dose ≥1,000 mg/day, the dose has been stabilized for at least 3 months) was administered to type 2 diabetic patients (240 patients) with poor metformin control alone. Systematic observation of the effects of Beinaglutide and metformin administered alone or in combination was conducted respectively.
The results of trials 5A and 5B showed that the effect of Beinaglutide was fast after injection, and the peak time was 20 minutes after administration. Despite its short duration of action (half-life of approximately 15 minutes), when combined with glipizide or metformin, it showed a better therapeutic effect than glipizide or metformin alone. Adverse events in Beinaglutide clinical trials were mainly mild to moderate nausea and vomiting, most of which can be tolerated by the subjects and relieved during medication.
Trial 5C was based on trial 5B, increasing the number of patients with type 2 diabetes, designing an expanded multicenter clinical trial protocol to further evaluate the effectiveness and safety of the combination of Beinaglutide (0.2 mg dose, three times a day, 0.2 mg each time) and oral hypoglycemic agents (metformin).
Table 10 (Trial 5A, in combination with glipizide), Table 11 (Trial 5B, in combination with metformin) and Table 12 (Trial 5C, in combination with metformin) showed 12-week BMI changes in patients with type 2 diabetes.
The body mass index of the three Beinaglutide groups (0.1 mg, 0.15 mg, and 0.2 mg) showed statistically significant (P<0.05) body weight loss at weeks 8 and 12 of treatment. In the 0.2 mg group, the body mass index (kg/m2) at the 12th week of treatment decreased by 0.79±0.79 (P<0.001), and the decrease was significantly different from the 0 mg dose group (P<0.05) (
The changes in body mass index of the three groups in the trial 5B were basically consistent with the changes in body weight. A 12-week comparison between groups showed that the body mass index of the 0.2 mg group reduced most significantly, with significant differences between the 0 mg and 0.1 mg groups (P=0.0000 and P=0.0020). There was no significant difference between the 0 mg and 0.1 mg groups (P=0.2317) (
As shown in Tables 10-11, when Beinaglutide was used in combination with glipizide or metformin, the BMI of the subject was significantly reduced in a dose-dependent manner.
Data from trial 5C were analyzed according to BMI criteria for overweight subjects (27.9≥BMI≥24.0 kg/m2) and obese patients (BMI≥28.0 kg/m2) (12 weeks of treatment (84 days)). Tables 12A, 12B and 13 show the effects of Beinaglutide on overweight and obese subjects, respectively (
Note: Covariance analysis was used for comparison between groups. The dependent variable was the change in body weight relative to baseline, and the covariate was baseline.
Body weight change from baseline=post-treatment−baseline. Data from 5C test data.
As shown in Tables 12 and 13, after 12 weeks of treatment, the proportion of subjects in the Beinaglutide+metformin group with the weight loss from the baseline ≥3% was 40.32%, and the proportion of subjects with weight loss ≥5% was 20.97. %, the decline rate of the control group (metformin alone group) was 27.27% and 10.39%, respectively. Paired T test and covariance analysis between groups were performed for the changes from baseline after treatment. All the p values were <0.05, and the differences were statistically significant. Statistical analysis showed that the Beinaglutide+metformin treatment group was superior to the control group in weight loss.
This example demonstrates the effects of various dosages of Beinaglutide injectable formulation on slowing stomach emptying in male and female rats. The Beinaglutide injectable formulation contains Beinaglutide of SEQ ID NO: 1 at 4.2 mg (42000 U) in 2.1 ml.
One hundred and twelve 8-week old Sprague-Dawley (SD) rats having a body weight of between 240 g and 287 g (male) or between 194 g and 227 g (female) were divided into 7 groups: Group 1 (buffer only control), Group 2 (Beinaglutide 10 μg/kg), Group 3 (Beinaglutide 12.5 μg/kg), Group 4 (Beinaglutide 15 μg/kg), Group 5 (Beinaglutide 30 μg/kg), Group 6 (Beinaglutide 45 μg/kg), and Group 7 (Beinaglutide 60 μg/kg). Various dosages of Beinaglutide solutions were prepared from the Beinaglutide injectable formulation, kept at room temperature for at least 3 hours before injecting the animals. The animals were fasted 29-33 hours before injection, and the animals were not given any water 5-7 hours before injection. Injections were made by subcutaneous administration to the neck, at 0.1 ml/100 g body weight. The experiment was carried as described in Example 1.
As shown in Tables 14 and 15 and
This example demonstrates the effects of various dosages of Beinaglutide injectable formulation on slowing stomach emptying in male diet induced obesity (DIO) mice. Except that a different animal model was used, the experiment was performed in the same way as described in Example 6.
Fifty-six C57BL6J mice between 4-6 weeks old were fed with high-fat diet (60% fat in calorie) and low-fat diet (10% fat in calorie), respectively, for 15 weeks until the body weight of the mice fed with high-fat diet significantly increased to 39.2-47.9 g.
As shown in Table 16 and
| Number | Date | Country | Kind |
|---|---|---|---|
| 201810198521.0 | Mar 2018 | CN | national |
This application is a continuation of International Patent Application No. PCT/CN2019/077541, filed Mar. 8, 2019, which claims the benefit of Chinese Patent Application No. 201810198521.0, filed Mar. 9, 2018, both of which are incorporated herein by reference in their entirety.
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/CN2019/077541 | Mar 2019 | US |
| Child | 17015500 | US |
