Patent Application
20230051463
The present invention relates to a pharmaceutical dosage form, in particular a solid dosage form for oral administration, comprising an active ingredient such as methotrexate or a pharmaceutically acceptable salt thereof, in particular in the form of pellets, including multiparticulates, mini-tablets and granulate. It further relates to oral dosage forms for which saturation kinetics limits the use of higher dosages of active ingredients.
Methotrexate oral formulations in the form of tablets are common on the market. Tablets comprising 2.5 mg methotrexate are sold by the companies TEVA, Sandoz and others.
According to Goodman et al. (Goodman et al, Outcomes Related to Methotrexate Dose and Route of Administration in Patients with Rheumatoid Arthritis: A Systematic Literature Review, Clin Exp Rheumatol, 2015) efficacy and toxicity of methotrexate appear related to absorbed dose of methotrexate, not to route of administration. While bioavailability is greater for parenteral methotrexate, there is no evidence yet that splitting the oral dose of methotrexate is less advantageous, safer or more tolerable than administering parenteral methotrexate. However, it appears to be beneficial to treat with higher doses of methotrexate, initially, and subsequently to switch to parenteral administration of methotrexate when the clinical response to an oral dose becomes inadequate.
According to Taylor et al (Taylor et al, How to Get the Most from Methotrexate (MTX) Treatment for Your Rheumatoid Arthritis Patients? — MTX in the Treat-to-Target Strategy”, Journal of Clinical Medicine, 2019) parenteral administration of methotrexate has the advantages of maximizing bioavailability, reducing gastrointestinal intolerance and potentially enhancing compliance and adherence.
The international patent application WO2007040997 describes an invention that relates to a pharmaceutical drug delivery system for the controlled release of absorption window active agents which have an absorption window in the gastrointestinal tract, i.e. are usually absorbed in the duodenum and/or jejunum or have a site of treatment in or proximal to the gastrointestinal tract or degrade in the colon.
The controlled-release dosage forms may provide good bioavailability of absorption window active agents. The document describes that anti-tumor agents allegedly suitable for the invention includes 5-cisplatin, doxorubicin, etoposide, fluorouracil, methotrexate, mitomycin, semustine, or mixtures of thereof.
WO2009132050 discloses auris formulations for treating otic diseases and conditions. It is suggested that the pharmaceutical ingredients may be delivered in a pulsatile manner comprising an immediate release and a delayed release of the active ingredient. However, the formulations disclosed are intended for localized, in auris, administration and are not suitable for oral administration.
For certain active ingredients having a narrow therapeutic index, such as methotrexate, the side effects have to be balanced very carefully against the efficacy upon choosing the administration route and administered dosage. For such active ingredients it is desirable to be able to vary the dosage for each individual patient. However, for some active ingredients, such as methotrexate, the use is further restricted by saturation kinetics. Increasing the amount of active ingredient in a single dosage form may only provide little or no improved clinical effect, due to saturation of active transport mechanisms from the gut lumen and into the blood stream, while increasing the side effects, due to uptake in non-target cells. For such active ingredients it may be desirable, not only to be able to vary the amount of active ingredient in a dosage form, but also to change the release profile, e.g. of an oral dosage form, according to the amount of active ingredient in the dosage form.
For the industrial manufacture of drugs, it is expensive and cumbersome to produce a large number of different pharmaceutical formulations with different strengths and release characteristics.
It is envisaged that the present concept may be used with one or more active ingredients, and may also be used with other active ingredients, such as chemotherapeutic agents.
Upon comparing subcutaneous and oral administration of methotrexate, oral administration of an immediate release formulation suffers from the drawback that saturation kinetics becomes prevalent when single dosages are increased above about 10-15 mg methotrexate or pharmaceutically equivalent of methotrexate. However, oral administration is very convenient for the patients.
In the art there exists a general understanding that methotrexate is actively taken up assisted by the folate transporter, and the uptake takes place mainly in the proximal jejunum. It has been described that absorption exhibits saturation when the available amount of methotrexate exceeds a certain limit. See e.g. Bannwarth et al. 1996, Clin. Pharmacokinet. Vol 30 p. 194-210; Grim et al 2003, Clin. Pharmacokinet. Vol 42 p.139-151; Hoekstra et al. 2004, J. Rheumatol. Vol. 31 p. 645-648; and Inoue and Yuasa 2014, Drug Metab. Pharmacokinet. Vol. 29 p 12-19. Some authors, e.g. van Roon and van der Laar 2010, Clin Exp Rheumatol Vol 28 (Suppl 61) p. S27-S32, have suggested to split higher dosages of Methotrexate in order to address this observed limitation in uptake.
Without being bound by theory, the present inventors speculates that methotrexate may also be efficiently taken up in the more distal part of the gastrointestinal tract and suggests that the limitation in methotrexate uptake in the proximal jejunum may be circumvented by formulating pharmaceutical compositions comprising methotrexate, where at least part of the methotrexate is released with a delayed release profile and therefore may be expected to have passed the proximal jejunum before the whole amount of methotrexate is released.
There is a need for an oral pharmaceutical composition with increased bioavailability of methotrexate at higher dose levels, such as 15 mg and more. Further, there is a need for an oral pharmaceutical composition with dose proportional increase in bioavailability of methotrexate at a dose level of 15 mg and more. In addition, there is a need for an oral pharmaceutical composition giving the patient the choice to spread the content of the composition on a meal, thus easing the administration. There is also a need for an easier method of manufacturing of a pharmaceutical product that is expected to be marketed in many different strengths.
Mini-tablet or pellet formulations are developed with immediate release profiles and with lag time/burst release profiles to deliver the dose in the intestine within maximum 4 hours from dosing. These different formulations can then be combined in a capsule or a sachet in an attempt to increase bioavailability compared to conventional tablets. The different mini-tablets or pellets may be combined in a single pharmaceutical formulation, e.g. a capsule or a sachet, in order to obtain a pharmaceutical dosage form with a particular preferred release profile of the active ingredient(s).
Methotrexate exists as either the acid (molecular weight: 454.4 g/mol) or the di-sodium salt (molecular weight: 498.40 g/mol). In pharmaceutical products, methotrexate is declared as the acid, but often added as the di-sodium salt (conversion factor 1.096), as this is freely soluble in water; the acid is practically insoluble in water. Here, in the case of doubt, the term “methotrexate” refers to methotrexate as well as pharmaceutically acceptable salts thereof. Amounts of methotrexate may refer to the acid form, and may also refer to pharmaceutically equivalent amounts of a salt thereof, such as the di-sodium salt.
Methotrexate is also known with names and formulas such as N-[4-[[2,4-Diamino-6-pteridinyl)methyl]methylamino]benzoyl]-L-glutamic acid; 4-amino-N10-methylpteroylglutamic acid, 4-amino-10-methylfolic acid, methylaminopterin, amethopterin, MTX, and C20H22N8O5.
In certain embodiments, the pharmaceutical composition is made by the technology as found in the international patent application WO2018011181, all of which is incorporated by reference in its entirety.
The international patent application WO2018011181 in the name of Contera Pharma and Solural Pharma describes a pulsatile drug delivery system that enables a delayed burst release of levodopa and DOPA decarboxylase inhibitors including carbidopa in the small intestine, thereby providing for improved management of morning akinesia in Parkinson's disease patients. The application comprises an aspect to provide a pulsatile release pharmaceutical composition comprising a. levodopa and a DOPA decarboxylase inhibitor, and b. a pulsatile release component providing for a predetermined lag time followed by a pulse release of said levodopa and said DOPA decarboxylase inhibitor. The application further describes an aspect to provide a pulsatile release pharmaceutical composition comprising, separately or together, a. a first pulsatile release component comprising levodopa, said first pulsatile release component providing for a predetermined lag time followed by a pulse release of levodopa, and b. a second pulsatile release component comprising a DOPA decarboxylase inhibitor, said second pulsatile release component providing for a predetermined lag time followed by a pulse release of said DOPA decarboxylase inhibitor. Mini-tablets comprising 2.8, 3.0, 4.0 mg levodopa and mini-tablets comprising 2.6 mg Carbidopa were described. 33 Levodopa mini-tablets coated to 25% weight gain and ten film coated Carbidopa mini-tablets were mixed and filled into a hard-shell gelatin capsule size 0. The capsule holds a dose of 100 mg levodopa+25 mg Carbidopa and the active component will be released after a lag-time; Carbidopa will be released followed by Levodopa.
According to an aspect, the invention concerns a pharmaceutical composition comprising a plurality of pellets, wherein each pellet has a smallest diameter 5 mm, preferably 3 mm, and wherein each pellet comprises methotrexate or a pharmaceutically acceptable salt thereof, or no methotrexate, and/or another active ingredient. The pellets may comprise one or more active pharmaceutical ingredients. Thus, the pellets may comprise methotrexate or a pharmaceutically acceptable salt thereof as the sole active ingredient.
A pharmaceutical composition is preferably a pharmaceutically acceptable composition, such as suitable for industrial production, marketing approval, and/or administration to humans and/or animals.
A “pellet” may be defined as a rounded, spherical or cylindrical body or medicine. The term “pellet” may further comprise a small ball or tube-shaped piece of any substance. A “pellet” may also refer to a small tablet, i.e. a mini-tablet, granulate, or multiparticulates. A pellet of the present invention is preferably spheronized or spherical, but may in principle have another suitable shape.
The term “smallest diameter” means that the pellet is able to pass through a circular aperture with this diameter, e.g. in the case of a cylindrical body it may be the diameter of the body, and the term diameter does not necessarily imply that the pellet is spherical.
The pyloric sphincter is a band of smooth muscle at the junction between the pylorus of the stomach and the duodenum of the small intestine. It plays an important role in digestion, where it acts as a valve to control the flow of partially digested food from the stomach to the small intestine. Liquids and smaller items get transported quickly through the pyloric sphincter. Larger items get transported during digestion, when the sphincter relaxes intermittently and aperture opens. Thus, a small pharmaceutical composition, preferably having a diameter 3 mm, may be emptied from the stomach independent of gastric emptying and transported to the duodenum irrespective of whether the subject has been eating or not.
According to another aspect, the invention concerns a pharmaceutical composition for oral administration comprising methotrexate or a pharmaceutically acceptable salt thereof, comprising a plurality of pellets, wherein each pellet has a smallest diameter 5 mm and wherein at least 80% of the total amount of methotrexate of said pharmaceutical composition have been released within 4 hours of administration and/or as measured in an USP Dissolution Apparatus 2 in 500 ml 0.1 N HCl at 37° C.±0.5° C.
According to another aspect, the invention concerns a pharmaceutical composition comprising a plurality of pellets, wherein each pellet comprises an active ingredient such as methotrexate or a pharmaceutically acceptable salt thereof, and preferably wherein at least one of the pellets provides immediate release of said active ingredient, such as methotrexate; and preferably wherein at least one of the pellets provides delayed release and/or a predetermined lag time prior to release of said active ingredient for dosages at 10 or 15 mg or above; and wherein at least 80% of the total amount of methotrexate of said pharmaceutical composition have been released within 4 hours of administration and/or as measured in an USP Dissolution Apparatus 2 in 500 ml 0.1 N HCl at 37° C.±0.5° C.
According to another aspect, the invention concerns a pharmaceutical composition comprising a plurality of pellets, wherein each pellet comprises methotrexate or a pharmaceutically acceptable salt thereof, and preferably wherein at least one of the pellets provides immediate release of said methotrexate; and preferably wherein at least one of the pellets provides delayed release and/or a predetermined lag time prior to release of methotrexate; and wherein at least 80% of the total amount of methotrexate of said pharmaceutical composition have been released within 4 hours of administration and/or as measured in an USP Dissolution Apparatus 2 in 500 ml 0.1 N HCl at 37° C.±0.5° C.
The total amount of released methotrexate after administration may preferably be measured in an USP Dissolution Apparatus 2, paddle (37° C.±0.5° C.).
According to another aspect, the invention concerns a pharmaceutical composition comprising
wherein said pharmaceutical composition allow release of at least 80% of the total methotrexate within 4 hours of administration.
According to another aspect, the invention concerns a pharmaceutical composition comprising
wherein said pharmaceutical composition allow release of at least 80% of the total methotrexate within 4 hours of administration.
According to another aspect, the invention concerns a pharmaceutical composition comprising a plurality of pellets, said composition comprising a total dosage of 1-30 mg methotrexate or a pharmaceutically acceptable salt thereof, and wherein said composition comprises:
According to another aspect, the invention concerns a pharmaceutical composition comprising a plurality of pellets, said composition comprising a total dosage of 1-30 mg methotrexate or a pharmaceutically acceptable salt thereof, and wherein said composition comprises:
According to another aspect, the invention concerns a pharmaceutical composition comprising a plurality of at least two, preferably at least three, pellets, providing a total dosage of methotrexate or a pharmaceutically acceptable salt thereof of 1-30 mg, wherein said composition comprises pellets providing immediate release of methotrexate;
and for dosages of 12.5-30 mg further comprises pellets providing delayed release of methotrexate;
and for dosages of 20-30 mg comprises pellets providing an additional delayed release of methotrexate.
According to another aspect, the invention concerns a pharmaceutical composition comprising a total amount of methotrexate, or a pharmaceutically acceptable salt thereof, of 15-50, preferably 20-30 mg, wherein said pharmaceutical composition releases at least 80% of the total amount of methotrexate within 4 hours; and wherein said pharmaceutical composition comprises
According to another aspect, the invention concerns a delayed release pharmaceutical composition comprising a content of methotrexate, or a pharmaceutically acceptable salt thereof, of at least 2.5 mg, more preferred at least 5 mg methotrexate, wherein said delayed release pharmaceutical composition releases less than 50% of said content of methotrexate within 1 hour;
for use in a treatment comprising oral administration of a total amount of methotrexate, or a pharmaceutically acceptable salt thereof, of 15-50, preferably 20-30 mg;
wherein said treatment further comprises administration of at least one immediate release pharmaceutical composition comprising 10-15 mg methotrexate and providing release of at least 8-10 mg of methotrexate within 1 hour, subject to the proviso than said delayed release pharmaceutical dosage forms and said immediate release pharmaceutical composition releases at least 80% of the total amount of methotrexate within 4 hours;
preferably each composition comprises one or more pellets, such as one or more tablets.
According to another aspect, the invention concerns an immediate release pharmaceutical composition comprising 10-15 mg methotrexate, or a pharmaceutically acceptable salt thereof, and providing release of at least 8-10 mg of methotrexate within 1 hour, for use in a treatment comprising oral administration of a total amount of methotrexate, or a pharmaceutically acceptable salt thereof, of 15-50, preferably 20-30 mg;
wherein said treatment further comprises administration of at least one delayed release pharmaceutical composition comprising a content of methotrexate, or a pharmaceutically acceptable salt thereof, of at least 2.5 mg, more preferred at least 5 mg methotrexate, wherein said delayed release pharmaceutical composition releases less than 50% of said content of methotrexate within 1 hour;
subject to the proviso that said delayed release pharmaceutical dosage forms and said immediate release pharmaceutical composition releases at least 80% of the total amount of methotrexate within 4 hours;
preferably each composition comprises one or more pellets, such as one or more tablets.
Having at least two, preferably at least three pellets, in the pharmaceutical formulation, with different release characteristics allow the release of methotrexate to be closer to saturation conditions without exceeding saturation in a subject.
Combining pellets with different release profiles may have the advantage from a manufacturing point of view that various release profiles may be obtained, e.g. for different dosages, by combining a few different types of pellets. As an example, 30 different release profiles for 30 different dosages may be obtained by mixing two or three different types of pellet. This provides a simplified production process as compared to the situation where 30 different tablets with different strengths and release profiles have to be manufactured, each with a specific composition. Using only a few different types of pellets to produce a large number of different pharmaceutical dosage forms simplifies logistics and storage, and/or may reduce the waste associated with having to handle a large number of different pharmaceutical dosage forms.
Further, the fact that the pharmaceutical compositions comprising different amount of methotrexate are available in similar pharmaceutical dosage forms may increase the patient compliance because patients can continue using the same dosage form that they are familiar with, even when the amount of methotrexate is changed. In this way patients may continue to take the same dosage form, which is familiar to them, throughout the whole lifetime, even though the amount of active ingredient(s) may be adjusted from time to time.
The ability to adjust the release profile to the strength of the dosage form allows for minimizing saturation kinetics and/or adverse effects and/or improving efficacy of the treatment.
According to an embodiment, pellet formulations are developed with immediate release and with lag time/burst release to deliver the dose in the intestine within maximum 4 hours from dosing. These different formulations can then be combined in a capsule or a sachet. The combination of immediate release and delayed release of methotrexate may increase bioavailability compared to conventional tablets.
According to another aspect, the invention concerns a pharmaceutical composition comprising a plurality of at least two, preferably at least three, pellets, providing a total dosage of methotrexate of 1-30 mg, wherein said composition comprises pellets providing immediate release of methotrexate; and for dosages of 7.5-20 mg further comprises pellets providing delayed release of methotrexate; and for dosages of 15-30 mg comprises pellets providing an additional delayed release of methotrexate.
According to another aspect, the invention concerns a method for the manufacture of a pharmaceutical composition according to the invention.
According to another aspect, the invention concerns a method for the manufacture of a pharmaceutical composition according to the invention comprising:
The method of manufacture according to the invention even allows for the manufacture of a pharmaceutical composition comprising low amounts of methotrexate, amounts below the limit where uptake is limited by uptake saturation, e.g. 1-10 mg methotrexate such a 1 mg, 2.5 mg or 5 mg; comprising only pellets providing for immediate release of the active ingredient(s).
According to another aspect, the invention concerns use of the pharmaceutical composition according to the invention in the manufacturing of a medicament for the treatment of a disease, wherein said disease is a disease according to the invention.
According to another aspect, the invention concerns a method of treating a disease according to the invention, comprising administering a therapeutically effective amount of the composition of the invention.
According to another aspect, the invention concerns a method of oral administration of a dosage form comprising a total amount of methotrexate, or a pharmaceutically acceptable salt thereof, of 15-50, preferably 20-30 mg, wherein said dosage form comprises
According to another aspect, the invention concerns a pharmaceutical composition comprising a plurality of pellets, wherein each pellet comprises methotrexate or a pharmaceutically acceptable salt thereof, and wherein at least one of the pellets provides immediate release of said methotrexate; and preferably wherein at least one of the pellets provides delayed release and/or a predetermined lag time prior to release of methotrexate;
and wherein at least 80% of the total amount of methotrexate of said pharmaceutical composition have been released within 4 hours of administration and/or as measured in an USP Dissolution Apparatus 2 in 500 ml 0.1 N HCl at 37° C.±0.5° C.
According to an aspect, the invention concerns a pharmaceutical composition obtainable according to a method of the invention.
According to an embodiment, the invention concerns a pharmaceutical composition comprising a plurality of pellets, wherein each pellet has a smallest diameter 5 mm, preferably 3 mm, and wherein each pellet comprises methotrexate or a pharmaceutically acceptable salt thereof.
According to an embodiment, the invention concerns a pharmaceutical composition for oral administration comprising methotrexate or a pharmaceutically acceptable salt thereof, comprising a plurality of pellets, wherein each pellet has a smallest diameter 5 mm and wherein at least 80% of the total amount of methotrexate of said pharmaceutical composition have been released within 4 hours of administration and/or as measured in an USP Dissolution Apparatus 2 in 500 ml 0.1 N HCl at 37° C.±0.5° C.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, comprising at least 10 mg methotrexate or a pharmaceutically acceptable salt thereof, wherein at least one of the pellets provides immediate release of said methotrexate; and at least one of the pellets provides delayed release and/or a predetermined lag time prior to release of methotrexate.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, comprising at least 15 mg methotrexate or a pharmaceutically acceptable salt thereof comprising:
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said at least one pellet providing immediate release of methotrexate, allows release of at least 90% of the active ingredient of said pellet in in 500 ml 0.1 N HCl, measured in a USP Dissolution Apparatus 2, Paddle, (37° C.±0.5° C.), within 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minute or within 30 minutes.
According to an embodiment, the invention concerns a pharmaceutical composition comprising a plurality of pellets, wherein each pellet comprises methotrexate or a pharmaceutically acceptable salt thereof, and preferably wherein at least one of the pellets provides immediate release of said methotrexate; and preferably wherein at least one of the pellets provides delayed release and/or a predetermined lag time prior to release of methotrexate; and wherein at least 80% of the total amount of methotrexate of said pharmaceutical composition have been released within 4 hours of administration and/or as measured in an USP Dissolution Apparatus 2 in 500 ml 0.1 N HCl at 37° C.±0.5° C.
The term “delayed release” refers to oral medicines that do not immediately disintegrate and release the active ingredient(s) into the body and may also refer to burst release or extended release.
The term “immediate release” refers to oral medicines that release the active ingredient(s) into the body without delay. Preferably immediate release means that at least 90% of the active ingredient is released within 30 minutes, more preferred at least 95% within 15 minutes, preferably at least 98% within 5 minutes.
The total amount of released methotrexate after administration may preferably be measured in an USP Dissolution Apparatus 2, paddle (37° C.±0.5° C.).
The amount of released active ingredient, such as methotrexate, may be measured in for example 500 ml 0.1 N HCl; 500 ml phosphate buffer pH 6.8; or 500 ml 0.9% saline.
According to an embodiment the invention concerns a pharmaceutical composition comprising
wherein said pharmaceutical composition allows release of at least 80% of the total methotrexate within 4 hours of administration.
According to an embodiment the invention concerns a pharmaceutical composition comprising
wherein said pharmaceutical composition allows release of at least 80% of the total methotrexate within 4 hours of administration.
According to an embodiment the invention concerns a pharmaceutical composition comprising a plurality of pellets, said composition comprising a total dosage of 1-30 mg methotrexate or a pharmaceutically acceptable salt thereof, and wherein said composition comprises:
According to an embodiment the invention concerns a pharmaceutical composition comprising a plurality of pellets, said composition comprising a total dosage of 1-30 mg methotrexate or a pharmaceutically acceptable salt thereof, and wherein said composition comprises:
Combining pellets with different release profiles has the advantage from a manufacturing point of view that various release profiles may be obtained, e.g. for different dosages, by combining a few different types of pellets. As an example, 30 different release profiles for 30 different dosages may be obtained by mixing two or three different types of pellet, instead of having to manufacture 30 different tablets with different strengths and release profiles.
The ability to adjust the release profile to the strength of the dosage form allows for minimizing saturation kinetics and/or adverse effects and/or efficacy of the treatment.
According to an embodiment, pellet formulations are developed with immediate release and with lag time/burst release to deliver the dose in the intestine within maximum 4 hours from dosing. These different formulations can then be combined in e.g. a capsule or sachet. The combination of immediate release and delayed release of methotrexate may increase bioavailability compared to conventional tablets.
According to an embodiment, the invention concerns a pharmaceutical composition comprising a plurality of at least one, preferably two, and optionally at least three, pellets, providing a total dosage of methotrexate or a pharmaceutically acceptable salt thereof of 1-30 mg, wherein said composition comprises pellets providing immediate release of methotrexate; and for dosages of 7.5-20 mg further comprises pellets providing delayed release of methotrexate; and for dosages of 15-30 mg preferably comprises pellets providing an additional delayed release of methotrexate.
According to an embodiment, the invention concerns a pharmaceutical composition comprising a plurality of at least two, preferably at least three, pellets, providing a total dosage of methotrexate or a pharmaceutically acceptable salt thereof of 1-30 mg, wherein said composition comprises pellets providing immediate release of methotrexate; and for dosages of 12.5-30 mg further comprises pellets providing delayed release of methotrexate; and for dosages of 20-30 mg preferably comprises pellets providing an additional delayed release of methotrexate.
According to an embodiment, the invention comprises a pharmaceutical composition comprising a total amount of methotrexate, or a pharmaceutically acceptable salt thereof, of 15-50 mg, preferably 20-30 mg, wherein said pharmaceutical composition releases at least 80% of the total amount of methotrexate within 4 hours; and wherein said pharmaceutical composition comprises
wherein said delayed release pharmaceutical composition releases less than 50% of said content of methotrexate within 1 hour; preferably each composition comprises one or more pellets, such as one or more tablets.
According to an embodiment, the invention comprises a delayed release pharmaceutical composition comprising a content of methotrexate, or a pharmaceutically acceptable salt thereof, of at least 2.5 mg, more preferred at least 5 mg methotrexate, wherein said delayed release pharmaceutical composition releases less than 50% of said content of methotrexate within 1 hour; for use in a treatment comprising oral administration of a total amount of methotrexate, or a pharmaceutically acceptable salt thereof, of 15-50, preferably 20-30 mg; wherein said treatment further comprises administration of at least one immediate release pharmaceutical composition comprising 10-15 mg methotrexate and providing release of at least 8-10 mg of methotrexate within 1 hour, subject to the proviso that said delayed release pharmaceutical dosage forms and said immediate release pharmaceutical composition releases at least 80% of the total amount of methotrexate within 4 hours; preferably each composition comprises one or more pellets, such as one or more tablets.
According to an embodiment, the invention comprises an immediate release pharmaceutical composition comprising 10-15 mg methotrexate, or a pharmaceutically acceptable salt thereof, and providing release of at least 8-10 mg of methotrexate within 1 hour, for use in a treatment comprising oral administration of a total amount of methotrexate, or a pharmaceutically acceptable salt thereof, of 15-50 mg, preferably 20-30 mg; wherein said treatment further comprises administration of at least one delayed release pharmaceutical composition comprising a content of methotrexate, or a pharmaceutically acceptable salt thereof, of at least 2.5 mg, more preferred at least 5 mg methotrexate, wherein said delayed release pharmaceutical composition releases less than 50% of said content of methotrexate within 1 hour; subject to the proviso that said delayed release pharmaceutical dosage forms and said immediate release pharmaceutical composition releases at least 80% of the total amount of methotrexate within 4 hours; preferably each composition comprises one or more pellets, such as one or more tablets.
According to an embodiment the invention provides a pharmaceutical composition comprising 2.5 mg, 5 mg, 7.5 mg, 10 mg, 12.5 mg, 15 mg, 17.5 mg, 20 mg, 22.5 mg, 25 mg, 27.5 mg, 30 mg or even higher amounts of methotrexate.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein each pellet has a size of less than 5.00 mm, 4.75 mm, 4.50 mm, 4.25 mm, 4.00 mm, 3.75 mm, 3.50 mm, 3.25 mm, 3.00 mm, 2.75 mm, 2.50 mm, 2.25 mm, 2.00 mm, 1.75 mm, 1.50 mm, 1.25 mm, 1.00 mm, 0.75 mm, 0.50 mm or less than 0.25 mm.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said pellets have a size selected among 0.01-5 mm, 0.1-4.5 mm, 0.2-4 mm, 0.3-3.5 mm, 0.4-3 mm, 0.5-2.5 mm, 0.6-2 mm, 0.75-1.5 mm, and about 1 mm.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein at least one of said pellets provides immediate release of methotrexate.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention comprising at least 10 or 15 mg methotrexate, wherein at least one of said pellets provides a predetermined delay of release of methotrexate.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention comprising at least 10 mg, preferably at least 12.5 mg, more preferred at least 15 mg methotrexate, wherein at least one of said pellets provides a predetermined delay of release of methotrexate.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein 0-40%, more preferred 5-35%, preferably 10-30%, more preferred 15-25%, preferably about 20% of the total amount of methotrexate has been released after 1 hour.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein 20-80%, more preferred 25-70%, preferably 30-60%, more preferred 35-50%, preferably about 40% of the total amount of methotrexate has been released after 2 hours.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein 30-100%, more preferred 40-90%, preferably 50-80%, more preferred 60-70%, preferably about 60% of the total amount of methotrexate has been released after 3 hours.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein 40-100%, more preferred 50-95%, preferably 60-90%, more preferred 70-85%, preferably about 80% of the total amount of methotrexate has been released after 4 hours.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein 20-90%, more preferred 30-80%, preferably 40-70%, more preferred at least 50% of the total amount of methotrexate has been released after 1 hour.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein 50-100%, more preferred 60-95%, preferably 65-90%, more preferred at least 70% of the total amount of methotrexate has been released after 2 hours.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein 60-100%, more preferred 70-99%, preferably 80-98%, more preferred more than 85% of the total amount of methotrexate has been released after 3 hours.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein 80-100%, more preferred 85-99%, preferably 90-98%, more preferred 93-97.5% of the total amount of methotrexate has been released after 4 hours.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention comprising an amount of methotrexate selected among at least 10, 12.5, 15, 20, 25 and 30 mg.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein the upper limit of release is valid for the total contents of the pharmaceutical composition selected among at least 10, 15, 20, 25 and 30 mg methotrexate.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein at least 80% of the total amount of methotrexate has been released within 4 hours, preferably 3 hours, of administration.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said at least one pellet providing immediate release of methotrexate, allows release of at least 80% or 90% of the active ingredient of said pellet in 500 ml 0.1 N HCl, measured in a USP Dissolution Apparatus 2, Paddle, (37° C.±0.5° C.), within 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes, 35 minutes, 40 minutes, 45 minutes, 50 minutes, 55 minutes, or within 60 minutes.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said at least one pellet providing immediate release of methotrexate, allows release of at least 80% or 90% of the active ingredient of said pellet in 500 ml 0.1 N HCl, measured in a USP Dissolution Apparatus 2, Paddle, (37° C.±0.5° C.), within 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, or within 30 minutes.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention comprising at least 15 mg methotrexate, wherein said at least one pellet providing delayed release and/or a predetermined lag time prior to release of methotrexate, allows release of at least 80% or 90% of the active ingredient of said pellet in 500 ml 0.1 N HCl, measured in an USP Dissolution Apparatus 2, Paddle, (37° C.±0.5° C.), within 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes, 35 minutes, 40 minutes, 45 minutes, 50 minutes, 55 minutes, 60 minutes, 65 minutes, 70 minutes, 75 minutes, 80 minutes, 85 minutes, 90 minutes, 95 minutes, 100 minutes, 105 minutes, 110 minutes, 115 minutes, 120 minutes, 125 minutes, 130 minutes, 135 minutes, 140 minutes, 145 minutes, 150 minutes, 155 minutes, 160 minutes, 165 minutes, 170 minutes, 175 minutes, 180 minutes, 185 minutes, 190 minutes, 195 minutes, 200 minutes, 205 minutes, 210 minutes, 215 minutes, 220 minutes, 225 minutes, 230 minutes, 235 minutes or within 240 minutes.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said at least one pellet providing delayed release and/or a predetermined lag time prior to release of methotrexate, allows release of at least 80% of the active ingredient of said pellet in 500 ml 0.1 N HCl, measured in an USP Dissolution Apparatus 2, Paddle, (37° C.±0.5° C.), within 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes, 35 minutes, 40 minutes, 45 minutes, 50 minutes, 55 minutes, 60 minutes, 65 minutes, 70 minutes, 75 minutes, 80 minutes, 85 minutes, 90 minutes, 95 minutes, 100 minutes, 105 minutes, 110 minutes, 115 minutes, 120 minutes, 125 minutes, 130 minutes, 135 minutes, 140 minutes, 145 minutes, 150 minutes, 155 minutes, 160 minutes, 165 minutes, 170 minutes, 175 minutes, 180 minutes, 185 minutes, 190 minutes, 195 minutes, 200 minutes, 205 minutes, 210 minutes, 215 minutes, 220 minutes, 225 minutes, 230 minutes, 235 minutes or within 240 minutes.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said at least one pellet providing delayed release and/or a predetermined lag time prior to release of methotrexate, allows release of at least 80% of the active ingredient of said pellet in 500 ml 0.1 phosphate buffer pH 6.8, measured in an USP Dissolution Apparatus 2, Paddle, (37° C.±0.5° C.), within 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes, 35 minutes, 40 minutes, 45 minutes, 50 minutes, 55 minutes, 60 minutes, 65 minutes, 70 minutes, 75 minutes, 80 minutes, 85 minutes, 90 minutes, 95 minutes, 100 minutes, 105 minutes, 110 minutes, 115 minutes, 120 minutes, 125 minutes, 130 minutes, 135 minutes, 140 minutes, 145 minutes, 150 minutes, 155 minutes, 160 minutes, 165 minutes, 170 minutes, 175 minutes, 180 minutes, 185 minutes, 190 minutes, 195 minutes, 200 minutes, 205 minutes, 210 minutes, 215 minutes, 220 minutes, 225 minutes, 230 minutes, 235 minutes or within 240 minutes.
According to an embodiment, the invention concerns the pharmaceutical composition according to any of the preceding claims, wherein said at least one pellet providing delayed release and/or a predetermined lag time prior to release of methotrexate, provides release of at least 80% of the active ingredient in 0.9% saline, measured in an USP Dissolution Apparatus 2, Paddle, (37° C.±0.5° C.), within 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes, 35 minutes, 40 minutes, 45 minutes, 50 minutes, 55 minutes, 60 minutes, 65 minutes, 70 minutes, 75 minutes, 80 minutes, 85 minutes, 90 minutes, 95 minutes, 100 minutes, 105 minutes, 110 minutes, 115 minutes, 120 minutes, 125 minutes, 130 minutes, 135 minutes, 140 minutes, 145 minutes, 150 minutes, 155 minutes, 160 minutes, 165 minutes, 170 minutes, 175 minutes, 180 minutes, 185 minutes, 190 minutes, 195 minutes, 200 minutes, 205 minutes, 210 minutes, 215 minutes, 220 minutes, 225 minutes, 230 minutes, 235 minutes or within 240 minutes.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention comprising at least 10 or 15 mg methotrexate, wherein said at least one pellet providing delayed release and/or a predetermined lag time prior to release of methotrexate, allows release of at least 80% or 90% of the active ingredient of said pellet in 500 ml 0.1 N HCl, measured in an USP Dissolution Apparatus 2, Paddle, (37° C.±0.5° C.), within 60 minutes, 65 minutes, 70 minutes, 75 minutes, 80 minutes, 85 minutes, 90 minutes, 95 minutes, 100 minutes, 105 minutes, 110 minutes, 115 minutes, 120 minutes, 125 minutes, 130 minutes, 135 minutes, 140 minutes, 145 minutes, 150 minutes, 155 minutes, 160 minutes, 165 minutes, 170 minutes, 175 minutes, 180 minutes, 185 minutes, 190 minutes, 195 minutes, 200 minutes, 205 minutes, 210 minutes, 215 minutes, 220 minutes, 225 minutes, 230 minutes, 235 minutes or within 240 minutes.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention comprising at least 10 or 15 mg methotrexate, wherein said at least one pellet providing delayed release and/or a predetermined lag time prior to release of methotrexate, provides release of less than 20% of the active ingredient of said pellet in 500 ml 0.1 N HCl, measured in an USP Dissolution Apparatus 2, Paddle, (37° C.±0.5° C.), within 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes, 35 minutes, 40 minutes, 45 minutes, 50 minutes, 55 minutes, 60 minutes, 65 minutes, 70 minutes, 75 minutes, 80 minutes, 85 minutes, 90 minutes, 95 minutes, 100 minutes, 105 minutes, 110 minutes, 115 minutes, 120 minutes, 125 minutes, 130 minutes, 135 minutes, 140 minutes, 145 minutes, 150 minutes, 155 minutes, 160 minutes, 165 minutes, 170 minutes, 175 minutes, 180 minutes, 185 minutes, 190 minutes, 195 minutes, 200 minutes, 205 minutes, 210 minutes, 215 minutes, 220 minutes, 225 minutes, 230 minutes, 235 minutes or within 240 minutes.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention comprising at least 10 or 15 mg methotrexate, wherein said at least one pellet providing delayed release and/or a predetermined lag time prior to release of methotrexate, provides release of less than 20% of the active ingredient of said pellet in 500 ml 0.1 N HCl, measured in an USP Dissolution Apparatus 2, Paddle, (37° C.±0.5° C.), within 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes, 35 minutes, 40 minutes, 45 minutes, 50 minutes, 55 minutes, or within 60 minutes.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said composition allows release of at least 80% of the active ingredient in 500 ml 0.1 N HCl, measured in an USP Dissolution Apparatus 2, Paddle, (37° C.±0.5° C.), within 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes, 35 minutes, 40 minutes, 45 minutes, 50 minutes, 55 minutes, 60 minutes, 65 minutes, 70 minutes, 75 minutes, 80 minutes, 85 minutes, 90 minutes, 95 minutes, 100 minutes, 105 minutes, 110 minutes, 115 minutes, 120 minutes, 125 minutes, 130 minutes, 135 minutes, 140 minutes, 145 minutes, 150 minutes, 155 minutes, 160 minutes, 165 minutes, 170 minutes, 175 minutes, 180 minutes, 185 minutes, 190 minutes, 195 minutes, 200 minutes, 205 minutes, 210 minutes, 215 minutes, 220 minutes, 225 minutes, 230 minutes, 235 minutes or within 240 minutes.
HCl may be referred to as hydrochloric acid.
A dissolution experiment may evaluate the rate and extent that a compound dissolves to form a solution under carefully controlled conditions.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said composition allows release of at least 80% of the active ingredient in 500 ml 0.1 N HCl, measured in an USP Dissolution Apparatus 2, Paddle, (37° C.±0.5° C.), within 60 minutes, 65 minutes, 70 minutes, 75 minutes, 80 minutes, 85 minutes, 90 minutes, 95 minutes, 100 minutes, 105 minutes, 110 minutes, 115 minutes, 120 minutes, 125 minutes, 130 minutes, 135 minutes, 140 minutes, 145 minutes, 150 minutes, 155 minutes, 160 minutes, 165 minutes, 170 minutes, 175 minutes, 180 minutes, 185 minutes, 190 minutes, 195 minutes, 200 minutes, 205 minutes, 210 minutes, 215 minutes, 220 minutes, 225 minutes, 230 minutes, 235 minutes or within 240 minutes.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said composition allows release of at least 80% of the active ingredient in 500 ml phosphate buffer pH 6.8, measured in a USP Dissolution Apparatus 2, Paddle, (37° C.±0.5° C.), within 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes, 35 minutes, 40 minutes, 45 minutes, 50 minutes, 55 minutes, 60 minutes, 65 minutes, 70 minutes, 75 minutes, 80 minutes, 85 minutes, 90 minutes, 95 minutes, 100 minutes, 105 minutes, 110 minutes, 115 minutes, 120 minutes, 125 minutes, 130 minutes, 135 minutes, 140 minutes, 145 minutes, 150 minutes, 155 minutes, 160 minutes, 165 minutes, 170 minutes, 175 minutes, 180 minutes, 185 minutes, 190 minutes, 195 minutes, 200 minutes, 205 minutes, 210 minutes, 215 minutes, 220 minutes, 225 minutes, 230 minutes, 235 minutes or within 240 minutes.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said composition allows release of at least 80% of the active ingredient in 500 ml phosphate buffer pH 6.8, measured in a USP Dissolution Apparatus 2, Paddle, (37° C.±0.5° C.), within 60 minutes, 65 minutes, 70 minutes, 75 minutes, 80 minutes, 85 minutes, 90 minutes, 95 minutes, 100 minutes, 105 minutes, 110 minutes, 115 minutes, 120 minutes, 125 minutes, 130 minutes, 135 minutes, 140 minutes, 145 minutes, 150 minutes, 155 minutes, 160 minutes, 165 minutes, 170 minutes, 175 minutes, 180 minutes, 185 minutes, 190 minutes, 195 minutes, 200 minutes, 205 minutes, 210 minutes, 215 minutes, 220 minutes, 225 minutes, 230 minutes, 235 minutes or within 240 minutes.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said composition allows release of at least 80% of the active ingredient in 0.9% saline, measured in a USP Dissolution Apparatus 2, Paddle, (37° C.±0.5° C.), within 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes, 35 minutes, 40 minutes, 45 minutes, 50 minutes, 55 minutes, 60 minutes, 65 minutes, 70 minutes, 75 minutes, 80 minutes, 85 minutes, 90 minutes, 95 minutes, 100 minutes, 105 minutes, 110 minutes, 115 minutes, 120 minutes, 125 minutes, 130 minutes, 135 minutes, 140 minutes, 145 minutes, 150 minutes, 155 minutes, 160 minutes, 165 minutes, 170 minutes, 175 minutes, 180 minutes, 185 minutes, 190 minutes, 195 minutes, 200 minutes, 205 minutes, 210 minutes, 215 minutes, 220 minutes, 225 minutes, 230 minutes, 235 minutes or within 240 minutes.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said composition allows release of at least 80% of the active ingredient in 0.9% saline, measured in a USP Dissolution Apparatus 2, Paddle, (37° C.±0.5° C.), within 60 minutes, 65 minutes, 70 minutes, 75 minutes, 80 minutes, 85 minutes, 90 minutes, 95 minutes, 100 minutes, 105 minutes, 110 minutes, 115 minutes, 120 minutes, 125 minutes, 130 minutes, 135 minutes, 140 minutes, 145 minutes, 150 minutes, 155 minutes, 160 minutes, 165 minutes, 170 minutes, 175 minutes, 180 minutes, 185 minutes, 190 minutes, 195 minutes, 200 minutes, 205 minutes, 210 minutes, 215 minutes, 220 minutes, 225 minutes, 230 minutes, 235 minutes or within 240 minutes.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention comprising at least 10 or 15 mg methotrexate, wherein at least one of the pellets comprises at least one excipient and/or coating controlling the release of said methotrexate.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein at least one of the pellets comprises at least one excipient and/or coating controlling the release of said methotrexate.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein at least one of the pellets comprises a coating controlling the release of methotrexate, wherein said coating comprises at least two excipients:
a. A first coating excipient; and
b. A second coating excipient, wherein said second coating excipient preferably has higher solubility than said first coating excipient; preferably said solubility is measured in an aqueous solvent, such as selected among water, 0.1 N HCl, phosphate buffer pH 6.8, and 0.9% saline.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein said first coating excipient is selected among ethyl cellulose, shellac, cellulose acetate, Eudragit RL (acrylic polymer), Eudragit RS, Eudragit NE (acrylcopolymer), Kollicoat SR 30 D (poly vinyl acetate), and a mixture of any of these.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein said second coating excipient is selected among hypromellose, methylcellulose, Polyethylene glycol (6000), Eudragit L, hypromellose acetate succinate, polyvinyl alcohol, and a mixture of any of these.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein said first coating excipient comprises ethyl cellulose and/or said second coating excipient comprises hypromellose.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein said coating comprises at least 15%, 14%, 13%, 12%, 11%, 10%, 9%, 8%, 7%, 6%, 5%, 4.5%, 4%, 3.5%, 3%, 2.9%, 2.8%, 2.7%, 2.6%, 2.5%, 2.4%, 2.3%, 2.2%, 2.1%, 2%, 1.9%, 1.8%, 1.7%, 1.6%, 1.5%, 1.4%, 1.3%, 1.2%, 1.1%, 1%, 0.9%, 0.8%, 0.7%, 0.6%, 0.5%, 0.4%, 0.3%, 0.2% or at least 0.1% w/w of said first coating excipient and/or said second coating excipient.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein said coating comprises more than 15%, 14%, 13%, 12%, 11%, 10%, 9%, 8%, 7%, 6%, 5%, 4.5%, 4%, 3.5%, 3%, 2.9%, 2.8%, 2.7%, 2.6%, 2.5%, 2.4%, 2.3%, 2.2%, 2.1%, 2%, 1.9%, 1.8%, 1.7%, 1.6%, 1.5%, 1.4%, 1.3%, 1.2%, 1.1%, 1%, 0.9%, 0.8%, 0.7%, 0.6%, 0.5%, 0.4%, 0.3%, 0.2% or at least 0.1% w/w of said first coating excipient and/or said second coating excipient.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein said first plurality of pellets comprises an amount selected among 2-20, 4—15, 6-10, and about 8% w/w of said first coating excipient and/or said second coating excipient.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein said second plurality of pellets comprises an amount selected among 0.1-15, 0.25-10, 0.5-5, 1-4, 1.5-3, and about 2% w/w of said first coating excipient and/or said second coating excipient.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein said third plurality of pellets comprises about an amount selected among 0.1-15, 0.25-10, 0.5-5, 1-4, 1.5-3, and about 1.8% w/w of said first coating excipient and/or said second coating excipient.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein at least one of the pellets comprises a core, such as a tablet, wherein said core comprises:
According to an embodiment, the invention concerns the pharmaceutical composition, wherein said at least one binder and/or filler is selected among the group consisting of saccharides and their derivatives, such as disaccharides (sucrose, lactose); polysaccharides and their derivatives, such as starches, cellulose or modified cellulose, such as microcrystalline cellulose, and cellulose ethers, such as hydroxypropyl cellulose (HPC); sugar alcohols such as xylitol, sorbitol or mannitol; protein such as gelatin; synthetic polymers, such as polyvinylpyrrolidone (PVP) and polyethylene glycol (PEG); and a mixture of any of these.
Preferably at least one excipient has suitable binding properties, and at least one excipient has suitable filling properties. It may be the same excipient which has both suitable binding and filling properties.
According to a preferred embodiment, at least one first excipient has suitable binding properties, while at least one second excipient has suitable filling properties.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein said at least one binder and/or filler is selected among the group consisting of microcrystalline cellulose, lactose monohydrate, and a mixture of these.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein said at least one disintegrant and/or dissolution excipient is selected among the group consisting of sodium starch glycolate, crosslinked polymers, such as crosslinked polyvinylpyrrolidone (crospovidone) or crosslinked sodium carboxymethyl cellulose (croscarmellose sodium), and a mixture of any of these.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein said at least one disintegrant and/or dissolution excipient is sodium starch glycolate.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein said at least one lubricant is selected among the group consisting of talc, silica, and fats, such as vegetable stearin, magnesium stearate or stearic acid, and a mixture of any of these.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein said at least one lubricant is magnesium stearate.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein the total amount of binder and filler is selected among 10—90, 20-80, 30-70, 40-60, 50-55, and about 52% w/w.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein the total amount of disintegrant and dissolution excipient is selected among 5-95, 10-90, 15-80, 20-70, 25-60, 30-50, 35-45 and about 40% w/w.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein the total amount of lubricant is selected among 0.1-5, 0.2-3, 0.3-2, 0.5-1.5 and about 1% w/w.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein said excipient and/or coating controlling the release of said methotrexate is ethyl cellulose and/or Hypromellose. Hypromellose may be referred to as HPMC.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said excipient and/or coating controlling the release of said methotrexate is ethyl cellulose added Hypromellose.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said coating comprises at least 15%, 14%, 13%, 12%, 11%, 10%, 9%, 8%, 7%, 6%, 5%, 4.5%, 4%, 3.5%, 3%, 2.9%, 2.8%, 2.7%, 2.6%, 2.5%, 2.4%, 2.3%, 2.2%, 2.1%, 2%, 1.9%, 1.8%, 1.7%, 1.6%, 1.5%, 1.4%, 1.3%, 1.2%, 1.1%, 1%, 0.9%, 0.8%, 0.7%, 0.6%, 0.5%, 0.4%, 0.3%, 0.2% or at least 0.1% Hypromellose.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said coating comprises more than 15%, 14%, 13%, 12%, 11%, 10%, 9%, 8%, 7%, 6%, 5%, 4.5%, 4%, 3.5%, 3%, 2.9%, 2.8%, 2.7%, 2.6%, 2.5%, 2.4%, 2.3%, 2.2%, 2.1%, 2%, 1.9%, 1.8%, 1.7%, 1.6%, 1.5%, 1.4%, 1.3%, 1.2%, 1.1%, 1%, 0.9%, 0.8%, 0.7%, 0.6%, 0.5%, 0.4%, 0.3%, 0.2% or at least 0.1% Hypromellose.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said first plurality of pellets comprises about 8% Hypromellose (This may be a Pellet A).
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said second plurality of pellets comprises about 2% Hypromellose (This may be a Pellet B).
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said third plurality of pellets comprises about 1.8% Hypromellose (This may be a Pellet C).
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said pharmaceutical composition is for oral administration.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein at least 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or at least 100% of the total methotrexate have been released within 4 hours.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said pellet comprises 0.1 mg-5 mg methotrexate, 0.15 mg-2 mg, 0.2 mg-1.5 mg, 0.25 mg-1 mg, 0.3 mg-0.8 mg, 0.35 mg-0.6 mg, 0.4 mg-0.5 mg, 0.45 mg-0.5 mg or about 0.45 mg methotrexate.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said composition comprises at least 2.5 mg, 5 mg, 7.5 mg, 10 mg, 12.5 mg, 15 mg, 17.5 mg, 20 mg, 22.5 mg, 25 mg, 27.5 mg or at least 30 mg methotrexate.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said composition comprises 2.5 mg, 5 mg, 7.5 mg, 10 mg, 12.5 mg, 15 mg, 17.5 mg, 20 mg, 22.5 mg, 25 mg, 27.5 mg, 30 mg or more than 30 mg methotrexate.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said composition comprises between 1 mg-50 mg methotrexate, between 2 mg-49 mg, 3 mg-48 mg, 4 mg-47 mg, 5 mg-46 mg, 6 mg-45 mg, 7 mg-44 mg, 8 mg-43 mg, 9 mg-42 mg, 10 mg-41 mg, 11 mg-40 mg, 12 mg-39 mg, 13 mg-38 mg, 14 mg-37 mg, 15 mg-36 mg, 16 mg-35 mg, 17 mg-34 mg, 18 mg-33 mg, 19 mg-32 mg, 20 mg-31 mg, 21 mg-30 mg, 22 mg-29 mg, 23 mg-28 mg, 24-27 mg, 25-26 mg or about 25 mg methotrexate.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein a plurality of pellets providing immediate release comprises a total of at least 2.5 mg, 5 mg, 7.5 mg, 10 mg, 12.5 mg, 15 mg, 17.5 mg, 20 mg, 22.5 mg, 25 mg, 27.5 mg or a total of at least 30 mg methotrexate.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein a plurality of pellets providing immediate release comprises a total of no more than 2.5 mg, 5 mg, 7.5 mg, 10 mg, 12.5 mg, 15 mg methotrexate.
Pharmaceutical compositions of the invention may have improved and/or excellent storage stability.
In one embodiment at least 80%, preferably at least 85%, more preferred at least 90% of the total amount of methotrexate in the pharmaceutical composition have been released within 4 hours of administration and/or as measured in an USP dissolution apparatus 2 in 500 mL 0.1 N HCl at 37° C.±0.5° C. after storage of said pharmaceutical composition at room temperature for 3 months.
In another embodiment at least 80%, preferably at least 85%, more preferred at least 90% of the total amount of methotrexate in the pharmaceutical composition have been released within 4 hours of administration and/or as measured in an USP dissolution apparatus 2 in 500 mL 0.1 N HCl at 37° C.±0.5° C. after storage of said pharmaceutical composition at room temperature for 6 months.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said composition is for use in a method of treatment of a disease and/or for use in a prophylaxis of a disease and/or for alleviating the symptoms of a disease.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said disease is an arthritis.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said arthritis is selected among Rheumatoid arthritis, juvenile idiopathic arthritis (and subsets thereof, such as Polyarticular) and or psoriasis arthritis.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said disease is selected among psoriasis, Crohn's disease and or a cancer.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said cancer is selected among a breast cancer, a cancer vesicae urinariae, choriocarcinoma, a head and neck cancer, a lymphoma and a leukemia.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention for use in a treatment, wherein the subject is a child or less than 18 years old.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein the pellets have color depending on their release characteristics.
Using different colors for different pellets depending on the release characteristics makes it possible to make quality check by visual inspection after the pellets have been mixed together to form the pharmaceutical composition. Further, patients may be able to verify the dosage, and different colors may increase patient compliance, in particular among younger patients such as children and for their parents assisting them in taking the treatment.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein each of said pellets is a tablet.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein a plurality of said pellets are compressed to form a tablet.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein said tablet is adapted to disintegrate in the stomach and/or small intestine of a subject.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said pellets are in a capsule or a sachet.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said composition comprises or is obtainable by combining a number of pellets selected among 1-200, 1-150, 1-120, 1-100, 1-90, 1-80, 1-70, 1-66, 1-60, 2-50, 3-40, 4-30, 5-25, 6-20, 7-18, 8-16, 9-14, 10-12, and 11 pellets.
According to an embodiment, the invention concerns the pharmaceutical composition according to the invention, wherein said composition is administered once a week, or twice within 12, preferably 8 hours, once a week.
According to an embodiment, the invention concerns a method for the manufacture of a pharmaceutical composition according to the invention.
According to an embodiment, the invention concerns a method for the manufacture of a pharmaceutical composition according to the invention comprising:
According to an embodiment, the invention concerns the method or pharmaceutical formulation according to the invention, wherein methotrexate is replaced or accompanied with one or more active ingredients, preferably wherein at least one active ingredient is a chemotherapeutic agent.
According to an embodiment, the invention concerns the method or pharmaceutical formulation according to the invention, wherein the composition further comprising one or more active ingredients in addition to methotrexate of a pharmaceutical acceptable salt thereof, preferably selected among chemotherapeutic agents.
According to an embodiment, the invention concerns the method or pharmaceutical formulation according to the invention, wherein the composition comprises 1-15 mg methotrexate or a pharmaceutically acceptable salt thereof and wherein the composition only comprises pellets providing immediate release of methotrexate.
According to an embodiment, the invention concerns the method or pharmaceutical formulation according to the invention, wherein the composition comprises 10-30 mg methotrexate or a pharmaceutically acceptable salt thereof and wherein the composition comprises pellets providing immediate release of methotrexate and pellets providing delayed release or a predetermined lag time before release of methotrexate.
According to an embodiment, the invention concerns the method or pharmaceutical formulation according to the invention, wherein the composition comprises 15-50 mg methotrexate or a pharmaceutically acceptable salt thereof, and wherein the composition comprises first pellets providing immediate release of methotrexate, second and one or more further pellets providing delayed release or a predetermined lag time before release of methotrexate and wherein the release of the one or more further pellets are slower than the release of methotrexate of the second pellets.
According to an embodiment, the invention concerns the use of methotrexate or a pharmaceutically acceptable salt thereof for the manufacture of a medicament for the treatment of a disease, such as a pharmaceutical composition according to the invention.
According to an embodiment, the invention concerns a method of treating the disease according to the invention, comprising administering a therapeutically effective amount of a composition of the invention.
According to an embodiment, the invention concerns a method of oral administration of a dosage form comprising a total amount of methotrexate, or a pharmaceutically acceptable salt thereof, of 15-50 mg, preferably 20-30 mg, wherein said dosage form comprises
wherein said delayed release pharmaceutical composition releases less than 50% of said content of methotrexate within 1 hour; subject to the proviso that said dosage form releases at least 80% of the total amount of methotrexate within 4 hours; preferably each composition comprises one or more pellets, such as one or more tablets.
According to an embodiment, the invention concerns a pharmaceutical composition comprising a plurality of pellets, wherein each pellet comprises methotrexate or a pharmaceutically acceptable salt thereof, and wherein at least one of the pellets provides immediate release of said methotrexate; and preferably wherein at least one of the pellets provides delayed release and/or a predetermined lag time prior to release of methotrexate;
and wherein at least 80% of the total amount of methotrexate of said pharmaceutical composition have been released within 4 hours of administration and/or as measured in an USP Dissolution Apparatus 2 in 500 ml 0.1 N HCl at 37° C.±0.5° C.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein at least 50% of the total amount of methotrexate has been released after 1 hour.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein 60-100% of the total amount of methotrexate has been released after 2 hours.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein 80-100% of the total amount of methotrexate has been released after 3 hours.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein 80-100% of the total amount of methotrexate has been released after 4 hours.
According to an embodiment, the invention concerns the pharmaceutical composition, comprising an amount of methotrexate selected among at least 10, 12.5, 15, 20, 25 and 30 mg.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein said disease is an inflammatory disease or a cancer.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein said inflammatory disease is selected among Rheumatoid arthritis, juvenile idiopathic arthritis, psoriasis and or psoriasis arthritis and said cancer is selected among
Acute Lymphocytic Leukemia or Chronic Lymphocytic Leukemia.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein said pellets are in a capsule or a sachet.
According to an embodiment, the invention concerns the pharmaceutical composition, for use in a treatment wherein said composition is administered once a week or twice within 12, preferably 8 hours once a week.
According to an embodiment, the invention concerns the pharmaceutical composition, comprising methotrexate, or a pharmaceutically acceptable salt thereof, as the sole active ingredient.
According to an embodiment, the invention concerns the pharmaceutical composition for oral administration.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein said pharmaceutical composition is or comprises a solid dosage form.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein the composition is formulated as a single dose formulation, such as a tablet, capsule or sachet.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein at least 80% of the total amount of methotrexate have been released within 4 hours of administration and/or as measured in an USP dissolution apparatus 2 in 500 mL 0.1 N HCl at 37° C.±0.5° C. after storage of said pharmaceutical composition at room temperature for 3 months.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein at least 85% of the total amount of methotrexate have been released within 4 hours of administration and/or as measured in an USP dissolution apparatus 2 in 500 mL 0.1 N HCl at 37° C.±0.5° C. after storage of said pharmaceutical composition at room temperature for 3 months.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein at least 90% of the total amount of methotrexate have been released within 4 hours of administration and/or as measured in an USP dissolution apparatus 2 in 500 mL 0.1 N HCl at 37° C.±0.5° C. after storage of said pharmaceutical composition at room temperature for 3 months.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein at least 80% of the total amount of methotrexate have been released within 4 hours of administration and/or as measured in an USP dissolution apparatus 2 in 500 mL 0.1 N HCl at 37° C.±0.5° C. after storage of said pharmaceutical composition at room temperature for 6 months.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein at least 85% of the total amount of methotrexate have been released within 4 hours of administration and/or as measured in an USP dissolution apparatus 2 in 500 mL 0.1 N HCl at 37° C.±0.5° C. after storage of said pharmaceutical composition at room temperature for 6 months.
According to an embodiment, the invention concerns the pharmaceutical composition, wherein at least 90% of the total amount of methotrexate have been released within 4 hours of administration and/or as measured in an USP dissolution apparatus 2 in 500 mL 0.1 N HCl at 37° C.±0.5° C. after storage of said pharmaceutical composition at room temperature for 6 months.
The straight line shows what the profile would look like if the release was linear.
All cited references are incorporated by reference.
The accompanying Figures and Examples are provided to explain rather than limit the present invention. It will be clear to the person skilled in the art that aspects, embodiments, claims and any items of the present invention may be combined.
Unless otherwise mentioned, all percentages are in weight/weight. Unless otherwise mentioned, all measurements are conducted under standard conditions (ambient temperature and pressure). Unless otherwise mentioned, test conditions are according to European Pharmacopoeia 8.0.
Development of Methotrexate Mini Tablets
Mini-tablet (or pellet) formulations are developed with immediate release and with lag time/burst release to deliver the dose in the intestine within maximum 4 hours from dosing. These different formulations can then be combined in a capsule and may increase bioavailability compared to conventional tablets. Different formulations may provide the desired amount of methotrexate and desired release profile(s).
Substances: Methotrexate disodium, Microcrystalline cellulose, Lactose monohydrate, Lactose Monohydrate (spraydried), Sodium starch glycolate, Magnesium stearate, Ethycellulose 7 cps, Hypromellose 3 cps, Ethanol 96%, Purified water.
Methotrexate exists as either the acid (molecular weight: 454.4) or the di-sodium salt (molecular weight: 498.40). In pharmaceutical products, Methotrexate is declared as the acid, but often added as the di-sodium salt (conversion factor 1.096), as this is freely soluble in water; the acid is practically insoluble in water.
Methotrexate di-sodium salt was sourced from Fermion, Finland.
Placebo mini-tablets for initial film coating experiments were produced in-house and were composed by Lactose monohydrate (67%), Microcrystalline cellulose (27%), Croscarmellose sodium (5%) and Magnesium stearate (1%) and compressed at a tooling similar to the size used for the Methotrexate mini-tablets.
Major Equipment Used is Listed in Table 1
Methods
The aim is a dose of 15 mg Methotrexate given with two or three release profiles, the first profile being immediate release (IR). Later profiles must deliver the dose within three-four hours post dosing.
With up to three release profiles, each profile can hold 5 mg dose. This was formulated in 11 mini-tablets each with tablet weight of 7.0 mg to be contained in a small capsule size (3*11 mini-tablets).
Excipients were chosen from those used in marketed products (e.g. Emthexate (TEVA) containing Microcrystalline cellulose, starch, magnesium stearate, silicon dioxide and lactose monohydrate).
Methotrexate Dissolution
Methotrexate dissolution was tested using the following parameters:
USP dissolution <711>, apparatus 2
Dissolution medium: 0.1 N HCl
500 mL dissolution medium, 75 RPM
Sample times: every half hour up to 6 hours.
Samples were quantified using HPLC or UV absorption at 303 nm.
Results and Discussion
Laboratory Experiments
First mixing experiments were a test of whether direct compression was possible or a granulation had to be introduced. Formulations were based on earlier experience with similar formulation principle (Table 2). In the second formulation Microcrystalline cellulose had been exchanged with Lactose monohydrate, otherwise formulations were identical.
The ingredients except magnesium stearate were mixed in the Turbula mixer at 22 rpm for 5 minutes in a 350 mL container. Magnesium stearate was added and mixed in for 1 minute.
Mini-tablets were compressed on the Diaf single punch tablet press using 2 mm tooling. In-process control was tablet weight (40 mini-tablets) and tablet thickness and friability (1 g product tested for 5 minutes at 45 rpm in Turbula mixer). The mix's compressed well; data are presented in Table 3.
A third batch, RD1907-3-T1, was compressed with same composition as RD1907-1-T1 to have enough mini-tablets for coating experiments.
Active mini-tablets were mixed with placebo mini-tablets to allow film coating in the STREA fluid-bed. As the active tablets were yellow from the API, mini-tablets could easily be sorted after coating. Typically, 10 g active mini-tablets were used; coating batch size was 300 g.
To achieve an IR formulation, mini-tablets were coated with a HPMC film (Table 4). Different barrier films based on ethylcellulose added hypromellose to form pores in the film, were produced and coated onto mini-tablets to achieve delayed burst release. By decreasing the content of hypromellose in the film, the film improved in delaying release.
Table 5 gives standard process parameters for film coating in STREA fluid-bed. At specified weight gains, the fluid-bed was stopped and samples drawn to be tested for dissolution.
IR Product
Batch RD1907-1-T1 was coated with the HPMC film as batch RD1907-1-T1-C1. The coating process was stopped at 15% weight gain, and the mini-tablets were tested in dissolution in three media: 0.1 N HCl, phosphate buffer pH 6.8 and 0.9% saline. 11 mini-tablets corresponding to 5 mg methotrexate were tested in 500 mL media at 75 rpm. Results are presented in
Delayed Release Products
Batch RD1907-1-T1 and RD1907-2-T1 were coated with the 20% HPMC film as batch RD1907-1-T1-C2 and RD1907-2-T1-C1 respectively, with sampling after 15%, 17.5% and 20% weight gain (
To achieve steeper release and a lag time, Batch RD1907-1-T1 and RD1907-3-T1 were coated with first 25% HPMC film (
With the 25% HPMC film, a lag time with no release was achieved with 15% weight gain or more. The release when first started was faster than for the 20% HPMC film but decreased with thickness of the film/weight gain.
With 20% weight gain, a lag time of 1-1½ hour was achieved and 80% of the dose was released after 3 hours. However, release rate from 2 hours onwards was low (10% every 30 min).
Very similar results were achieved with the 22.5% HPMC film but with lower weight gain. 15% weight gain with this film gave same result as 20% weight gain with the 25% HPMC film. With the 22.5% HPMC film it was possible to achieve longer lag-time and still have a acceptable release rate.
Mini-tablets with different release profiles all releasing the Methotrexate between 15 minutes and 4 hours have been developed. From these formulations, two or three release profiles can be selected to deliver the dose at intervals over the stomach and intestine.
A combination of two equal doses of immediate release MTX (ka=1,48) and slow release MTX (simulated to be released (ka=0.22) at two hours after first dose) seems to give high exposure of MTX. The second dose is expected to have a lower bioavailability of 80% in comparison to the first dose, due to less effective absorption from the lower part of the small intestine. A release that gives rise to a plasma concentration lower than approximately 200 ng/ml is believed to be in the linear range of absorption from the gut of MTX. A combination of mini-tablets with different in-vitro release profiles may result in better bioavailability mimicking the pharmacokinetic profiles of subcutaneous dosing of MTX.
The experiments and calculations indicate an immediate release profile in combination with RD1907-3-T1-C1 20% as well as RD1907-3-T1-C2 17.5% WG is believed to offer the best combination of mini-tablets.
Profile 1 may be substituted with profile 2, profile 6 may be substituted with profile 3, 4, 5 or 6B and profile 10 may be substituted with profile 7, 8 or 9.
The simulated and proposed combinations have been based on the following data and results:
In this example minitablets were prepared using methods essentially as described in example 1.
A mixture of the following ingredients was prepared:
The mixture was obtained by mixing all ingredients except magnesium stearate for 5 minutes in a Turbala mixer for 5 minutes, whereafter magnesium stearate was added and mixing continued for another 60 s.
The mixture was compressed into minitablets using the Diaf single punch tablet press using 2 mm tooling.
The formed mini-tablets each comprised 0.417 mg methotrexate (corresponding to that 12 mini-tablets in total comprise 5 mg methotrexate). The minitablets were coated and colored according to the release profile. The following mini-tablets were prepared:
The ER minitablets provided delayed release of methotrexate and the release of methotrexate were slower for ER minitablets B in comparison with ER minitablets A.
Subsequent pharmaceutical compositions, in form of capsules, were prepared using combinations of these mini-tablets:
Capsules comprising 5 mg or 10 mg metothrexate, comprising only immediate release pellets and capsules comprising 15 mg, 20 mg or 25 mg, comprising both immediate release pellets and delayed release pellets were provided as described in Example 1.
Capsules were placed in closed containers at room temperature (25° C.) and 60% relative humidity, and stored for 3 months.
The dissolution profiles were determined for the capsules in the beginning (T=0) and after 3 months storage.
Dissolution profiles at time 0:
Dissolution profile after 3 months storage at 25° C. and 60% relative humidity:
The results show that the pharmaceutical composition have the desired release profiles, more than 80% release after 4 hours, and maintain the desired release profiles after 3 months storage under the selected conditions (25° C., 60% relative humidity).
| Number | Date | Country | Kind |
|---|---|---|---|
| 20153818.8 | Jan 2020 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/DK2021/050025 | 1/26/2021 | WO |
