原研机构 |
非在研机构- |
最高研发阶段临床3期 |
首次获批日期- |
最高研发阶段(中国)临床3期 |
特殊审评- |
开始日期2024-04-30 |
申办/合作机构 |
开始日期2023-12-06 |
申办/合作机构 |
开始日期2023-11-06 |
申办/合作机构 |
适应症 | 最高研发状态 | 国家/地区 | 公司 |
---|---|---|---|
特应性皮炎 | 临床3期 | 中国 更多 | |
慢性鼻窦炎伴鼻息肉 | 临床申请批准 | 中国 更多 | |
哮喘 | 终止 | 中国 更多 |
研究 | 分期 | 人群特征 | 评价人数 | 分组 | 结果 | 评价 | 发布日期 |
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临床1期 | IL-4 | IL-13 | 40 | 夢願鏇憲蓋選範糧積鬱(齋鏇窪簾顧鬱顧願構餘) = A total of 28 (87.5%) subjects received AK120 treatment and 7 (77.8%) subjects received placebo experienced at least one treatment-emergent adverse event (TEAE). All TEAEs were mild and moderate in severity. 12 (37.5%) subjects experienced at least one treatment-related TEAEs in the AK120 treatment group, and 4 (44.4%) subjects in the placebo group. The most common TEAEs occurred in AK120 treatment group were skin infection (12.5%) and injection site pain (12.5%). There was no death, no serious adverse event (SAE) or treatment-related SAE in the study. 積築範遞鏇願襯簾觸遞 (鹽蓋範糧築願餘餘鑰選 ) | 积极 | 2023-10-11 | ||
Placebo | |||||||
临床1期 | IL-4 receptor alpha (IL-4Rα) | IL-4 | IL-13 | 40 | 廠鹽網遞襯衊淵夢構壓(壓構簾鏇範衊願憲糧夢) = 構顧蓋觸遞艱糧艱鬱廠 齋齋簾鏇夢醖衊顧窪蓋 (廠製鹹鏇鹹鑰鹹醖鑰遞 ) 更多 | 积极 | 2022-09-07 | ||
廠鹽網遞襯衊淵夢構壓(壓構簾鏇範衊願憲糧夢) = 鹽選齋構衊艱廠範積選 齋齋簾鏇夢醖衊顧窪蓋 (廠製鹹鏇鹹鑰鹹醖鑰遞 ) 更多 |