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Drug Highest PhaseApproved |
First Approval Ctry. / Loc.US |
First Approval Date15 Oct 2014 |
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MechanismM3 receptor antagonists [+1] |
Active Org.- |
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Active Indication- |
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Drug Highest PhaseDiscontinued |
First Approval Ctry. / Loc.- |
First Approval Date- |
在一线化疗失败的晚期非小细胞肺癌患者中,评价BIBF 1120或安慰剂联合多西他赛治疗的有效性和安全性
[Translation] To evaluate the efficacy and safety of BIBF 1120 or placebo combined with docetaxel in patients with advanced non-small cell lung cancer who have failed first-line chemotherapy
在接受一线化疗失败后的IIIB/IV期或复发性非小细胞肺癌患者中,比较接受BIBF 1120加标准多西他赛治疗与安慰剂加标准多西他赛治疗的有效性和安全性,生活质量和BIBF1120药代动力学的数据也将进行分析。
[Translation] The efficacy and safety of BIBF 1120 plus standard docetaxel versus placebo plus standard docetaxel in patients with stage IIIB/IV or recurrent NSCLC who have failed first-line chemotherapy will also be analyzed, as will data on quality of life and pharmacokinetics of BIBF1120.
100 Clinical Results associated with Meilaipu (Beijing) Pharmaceutical Research Co., Ltd.
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100 Deals associated with Meilaipu (Beijing) Pharmaceutical Research Co., Ltd.
100 Translational Medicine associated with Meilaipu (Beijing) Pharmaceutical Research Co., Ltd.