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MechanismNF-kappa-B-repressing factor inhibitors |
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Inactive Indication- |
Drug Highest PhaseApproved |
First Approval Ctry. / Loc.CN |
First Approval Date23 Jul 2004 |
尿多酸肽注射液(CDA-Ⅱ)治疗低危、中危-1 骨髓增生异常综合征(MDS)随机开放、多中心II 期临床研究
[Translation] A randomized, open, multicenter phase II clinical study of CDA-Ⅱ in the treatment of low-risk and intermediate-risk myelodysplastic syndrome (MDS)
主要目的:评价CDA-Ⅱ治疗IPSS 评分为低危、中危-1 的MDS 患者的血液学改善(HI)率; 次要目的:输血需求变化、观察完全缓解(CR)和部分缓解(PR)、血液学改善(HI)维持时间、生活质量(QLQ)和安全性。
[Translation] Primary objective: To evaluate the hematological improvement (HI) rate of MDS patients with low-risk and intermediate-risk-1 IPSS scores treated with CDA-Ⅱ; Secondary objectives: Changes in transfusion requirements, observation of complete remission (CR) and partial remission (PR), duration of hematological improvement (HI), quality of life (QLQ) and safety.
喜滴克(尿多酸肽注射液)联合化疗治疗晚期乳腺癌、非小细胞肺癌开放、多中心IV 期临床试验
[Translation] An open, multicenter Phase IV clinical trial of Xidic (uropolyacitide injection) combined with chemotherapy for the treatment of advanced breast cancer and non-small cell lung cancer
旨在评价国家I 类抗癌新药喜滴克上市后联合化疗用于治疗晚期乳腺癌、非 小细胞肺癌的安全性和临床获益。
[Translation] The aim is to evaluate the safety and clinical benefits of Xidic, a national Class I anticancer new drug, combined with chemotherapy for the treatment of advanced breast cancer and non-small cell lung cancer after its launch.
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