SALTS AND CRYSTALS
    3.
    发明公开
    SALTS AND CRYSTALS 审中-公开

    公开(公告)号:US20240287074A1

    公开(公告)日:2024-08-29

    申请号:US18044190

    申请日:2021-09-07

    摘要: This invention relates to solid forms of 1-methyl-1,4,5, IO-tetrahydropyrazolo[3,4-b][1,5]benzodiazepine freebase possessing desirable pharmacokinetic properties, such as low hygroscopicity and improved thermal stability. These solid forms include a crystalline form of 1-methyl-1,4,5,IO-tetrahydropyrazolo[3,4-b][1,5]benzodiazepine 5 freebase and phosphate and L-tartrate salts of 1-methyl-1,4,5,IO-tetrahydropyrazolo[3,4-b][1,5]benzodiazepine freebase. Pharmaceutical compositions, medicaments and kits comprising these solid forms are also described. Also provided are methods of using these forms to treat various diseases, conditions and disorders.

    METHODS OF TREAMENT
    5.
    发明公开
    METHODS OF TREAMENT 审中-公开

    公开(公告)号:US20240216392A1

    公开(公告)日:2024-07-04

    申请号:US18524124

    申请日:2023-11-30

    IPC分类号: A61K31/5517 A61P25/08

    CPC分类号: A61K31/5517 A61P25/08

    摘要: Provided herein are treatment methods including administering a 5-hydroxytryptamine (HT)2C receptor agonist to a patient in need thereof. An exemplary method includes treating or preventing a 5-hydroxytryptamine (HT)2C receptor-associated disorder in a patient in need thereof, wherein the method comprises administering to the patient (R)—N-(2,2-difluoroethyl)-7-methyl-1,2,3,4,6,7-hexahydro-[1,4]diazepino[6,7,1-hi]indole-8-carboxamide (Compound 1), or a pharmaceutically acceptable salt thereof, wherein Compound 1, or a pharmaceutically acceptable salt thereof, is administered twice daily.

    MIDAZOLAM AND KETAMINE FOR ENHANCED SEDATION

    公开(公告)号:US20240207285A1

    公开(公告)日:2024-06-27

    申请号:US18390923

    申请日:2023-12-20

    发明人: Larry Dillaha

    摘要: Provided herein are pharmaceutical compositions comprising midazolam and ketamine, and methods of inducing sedation (e.g., procedural sedation) in a subject using administration of such compositions, the compositions optionally including a pharmaceutically active compound of a third class. Compositions may be in sublingual or buccal form, or incorporated into vehicles for extended release. Methods for fabricating the compositions and using them for anesthesiological applications are also described.