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相关临床试验
35
1 进行中
药物批准
0
批准总数
监管机构
监管机构数
成立时间
N/A
已完成
19
54.3%
尚未招募
1
2.9%
招募中
14
40.0%
撤回
暂无批准数据
- Lumosa Therapeutics' LT3001 demonstrated a robust safety profile and tolerability in a Phase II clinical trial for acute ischemic stroke patients. - The trial, conducted by Shanghai Pharma, showed comparable adverse event rates between LT3001 and placebo groups over 90 days. - Preliminary efficacy data indicated a promising proportion of patients achieving favorable outcomes on the modified Rankin Scale (mRS) at Day 90 post-treatment. - Lumosa plans to collaborate with Shanghai Pharma and seek international licensing to advance LT3001's global development for stroke treatment.