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公开(公告)号:US20240173294A1
公开(公告)日:2024-05-30
申请号:US18434065
申请日:2024-02-06
CPC分类号: A61K31/4045 , A61K9/0056 , A61K47/12 , A61K47/26 , A61K47/36 , A61K47/46
摘要: The present invention relates to a composition comprising melatonin encapsulated within a calcium alginate hydrogel. It further provides an orally administrable dosage form comprising such a composition held within a gel, wherein the gel is formed using starch as a gelling agent. Processes to produce these compositions, as well as their use in therapy, are also disclosed.
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公开(公告)号:US20240173263A1
公开(公告)日:2024-05-30
申请号:US17793540
申请日:2021-12-28
发明人: Xufa Li , Jiewei Chen
CPC分类号: A61K9/4816 , A61K47/10 , A61K47/26 , A61K47/36
摘要: The invention relates to a soft capsule shell and a soft capsule. The present invention provides soft capsule shells prepared from a film-forming composition including 2 wt % to 5 wt % of a first gelling agent, 10 wt % to 35 wt % of a plasticizer, 18 wt % to 35 wt % of gelatinizable starch, 4 wt % to 17 wt % of granular starch, and 35 wt % to 55 wt % of water, wherein the first gelling agent is a gellan gum having a weight-average molecular weight of 5.0×105 to 8.0×106 g/mol and/or a coefficient of molecular weight distribution of 1.0 to 6.0. The film-forming composition provided by the invention has good film-forming mechanical strength, toughness and viscosity, is good in seaming when being compressed into soft capsules, and can be disintegrated in medium water and simulated gastric juice.
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公开(公告)号:US20240166636A1
公开(公告)日:2024-05-23
申请号:US18471734
申请日:2023-09-21
申请人: Epizyme, Inc.
发明人: Marinus Jacobus VERWIJS , David Jon AM ENDE , Stephen Richard ANDERSON , Andrew Paul George BEEVERS , Mark Kenneth BREAULT , Stephen Richard TUDHOPE , Jamie Ross WOLSTENHULME
CPC分类号: C07D405/12 , A61K9/14 , A61K47/12 , A61K47/26 , A61K47/36 , A61K47/38 , C07B2200/13
摘要: Provided herein are methods for making a crystalline form of N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-5-(ethyl (tetrahydro-2H-pyran-4-yl)amino)-4-methyl-4′-(morpholinomethyl)-[1,1′-biphenyl]-3-carboxamide hydrobromide and related products, compositions and treatment methods.
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公开(公告)号:US20240165190A1
公开(公告)日:2024-05-23
申请号:US18281545
申请日:2022-03-11
摘要: The present disclosure relates to a herbo-mineral metallic pharmaceutical kit for delaying/controlling recurrence and/or metastasis of cancer in Triple Negative Breast Cancer (TNBC) patients. The herbo-mineral metallic pharmaceutical kit comprises a first container containing Suvarna Bhasmadi Vati (SBV), a second container containing Mouktikyukta Kamdudha Vati (MKV), a third container containing Shatavari Vati (SV), a fourth container containing Arogyavardhini Vati (AVV), a fifth container containing Triphala Guggul Vati (TGV) and a sixth container containing jatamansi Oil (JMO). The herbo mineral metallic pharmaceutical kit assists in improving immunomodulatory response and reducing oxidative stress in TNBC patients.
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公开(公告)号:US20240165141A1
公开(公告)日:2024-05-23
申请号:US18291880
申请日:2022-07-25
发明人: David Friend , Jennifer Kiang , Nicolas J. Pacelli , Mark Walters
CPC分类号: A61K31/7056 , A61K9/0034 , A61K9/06 , A61K47/10 , A61K47/36 , A61P15/02
摘要: A pharmaceutical composition for use in the treatment of bacterial vaginosis, wherein said composition comprises a poloxamer, a stabilization polymer, and an active ingredient for treating the bacterial vaginosis, preferably clindamycin, wherein said composition has a viscosity of at least 1.5 million mPa·s.
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公开(公告)号:US20240165024A1
公开(公告)日:2024-05-23
申请号:US18422105
申请日:2024-01-25
CPC分类号: A61K9/0095 , A61K9/0053 , A61K9/10 , A61K47/02 , A61K47/10 , A61K47/14 , A61K47/26 , A61K47/36
摘要: Disclosed herein is a pharmaceutical oral suspension, comprising: mycophenolate mofetil in an amount of about 200 mg/mL; one or more cosolvents comprising ethanol, a polyethylene glycol, a sorbitol, glycerin, propylene glycol, benzyl alcohol, or a combination thereof in an amount of from about 5% w/w to about 30% w/w; one or more pharmaceutically acceptable excipients selected from a suspending agent, a preservative, a sweetener, an antifoaming agent, a wetting agent, a buffering agent, and a flavoring agent; and a vehicle comprising water. The pharmaceutical oral suspension has improved stability, palatability with high dose of active ingredient.
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公开(公告)号:US11986528B2
公开(公告)日:2024-05-21
申请号:US17443485
申请日:2021-07-27
申请人: GATTEFOSSE SAS
发明人: Amandine Forest , Jean-David Rodier
CPC分类号: A61K47/36 , A61K9/1682 , A61K47/10
摘要: The invention concerns the use, as a pharmaceutical or cosmetic excipient, of a composition which is solid at ambient temperature and in the form of individualized particles, said composition comprising:
lauroyl macrogolglyceride,
polyethylene glycol.-
公开(公告)号:US20240157101A1
公开(公告)日:2024-05-16
申请号:US18550371
申请日:2022-03-18
发明人: David H. Gracias , Florin M. Selaru , Arijit Ghosh
CPC分类号: A61M31/002 , A61K9/0031 , A61K9/0053 , A61K47/36
摘要: The present disclosure provides microscale devices, systems, and methods thereof for the delivery of therapeutic and prophylactic active agents (e.g., macromolecules).
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公开(公告)号:US20240156839A1
公开(公告)日:2024-05-16
申请号:US18548741
申请日:2022-03-04
发明人: Sheue-Fang SHIH , Hsin-Yi CHIU
CPC分类号: A61K31/573 , A61K9/0019 , A61K9/0048 , A61K9/06 , A61K9/1272 , A61K47/36 , C07K16/22 , A61K2039/54 , C07K2317/24
摘要: Provided is a pharmaceutical composition for delivery of an active agent to an eye. The pharmaceutical composition may comprise a lipid mixture; an active agent and a biocompatible hydrogel. The pharmaceutical composition achieves a prolonged therapeutic effect as well as reduced side effects. Also provided is a method of delivering an active agent in the pharmaceutical composition to an eye of a subject in need thereof.
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公开(公告)号:US20240156793A1
公开(公告)日:2024-05-16
申请号:US18057941
申请日:2022-11-22
申请人: Lumos Pharma, Inc.
发明人: Alpa B. PARIKH , John C. McKEW
CPC分类号: A61K31/438 , A61K9/2077 , A61K9/2846 , A61K47/24 , A61K47/26 , A61K47/36 , A61K47/38 , A61P5/06
摘要: The present disclosure relates to pharmaceutical solid forms and pharmaceutical compositions comprising ibutamoren or a pharmaceutically acceptable salt thereof, and methods for administering to a pediatric subject for treating growth hormone deficiency.
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