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隶属于 C.H. Boehringer Sohn AG & Co. KG
相关临床试验
358
190 进行中
药物批准
252
批准总数
监管机构
3
监管机构数
成立时间
N/A
进行中(未招募)
184
51.4%
已完成
53
14.8%
尚未招募
6
1.7%
招募中
107
29.9%
暂停
2
0.6%
Unknown
4
1.1%
NMPA
National Medical Products Administration
102
EMA
European Medicines Agency
27
CIMA_AEMPS
Spanish Agency for Medicines and Medical Devices
123
- Phase 2 AIRLEAF trial results indicate that BI 1291583, a cathepsin C inhibitor, reduces the risk of pulmonary exacerbations in adults with bronchiectasis. - The study showed a dose-dependent benefit of BI 1291583 compared to placebo in time to first pulmonary exacerbation over 48 weeks. - A 29% decreased risk of initial pulmonary exacerbation was observed with the 5 mg dose of BI 1291583 compared to placebo, though statistical significance was not reached. - A phase 3 trial (AIRTIVITY) is planned for 2025 to further evaluate BI 1291583 in bronchiectasis patients.