|
|
|
|
|
|
最高研发阶段批准上市 |
|
首次获批日期2018-06-25 |
|
|
|
|
|
|
最高研发阶段批准上市 |
|
首次获批日期1985-05-31 |
靶点- |
作用机制- |
|
|
|
非在研适应症- |
最高研发阶段临床阶段不明 |
首次获批国家/地区- |
首次获批日期- |
A Multicenter, Open-Label Study to Assess the Long-Term Safety of Pharmaceutical Grade Synthetic Cannabidiol Oral Solution in Patients With Prader-Willi Syndrome
The objective of this study is to assess the long-term safety and tolerability of Cannabidiol Oral Solution (CBD) in participants with Prader-Willi Syndrome.
A Multicenter, Open-Label, Flexible Dose Study to Assess the Long-Term Safety of Pharmaceutical Grade Synthetic Cannabidiol Oral Solution in Pediatric Patients With Treatment-Resistant Childhood Absence Seizures
The primary purpose of this study is to assess the long-term safety and tolerability of Cannabidiol Oral Solution (CBD) in pediatric participants with treatment-resistant childhood absence seizures.
100 项与 Benuvia Therapeutics, Inc. 相关的临床结果
0 项与 Benuvia Therapeutics, Inc. 相关的专利(医药)
100 项与 Benuvia Therapeutics, Inc. 相关的药物交易
100 项与 Benuvia Therapeutics, Inc. 相关的转化医学