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最高研发阶段批准上市 |
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首次获批日期2010-06-17 |
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最高研发阶段批准上市 |
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首次获批日期2004-05-19 |
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最高研发阶段批准上市 |
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首次获批日期1999-06-16 |
A multicenter, randomized, open label, two treatment, two period,two sequence, single-dose, crossover, bioequivalence study ofMethotrexate Tablets 2.5 mg (manufactured for Actavis LLC) withMethotrexate Tablets USP 2.5 mg (DAVA Pharmaceuticals, Inc.,Fort Lee, NJ 07024 USA) in patients with mild to severe psoriasisor rheumatoid arthritis (RA), who are already on establishedregimens of 2.5 mg every 12 hours under fasting condition. - NA
A randomized, open label, multi centric, two treatment, two period, two sequence, single dose, crossover, bioequivalence study of Paclitaxel protein-bound particles for injectable suspension (albumin-bound) 100 mg/vial manufactured by Sindan Pharma for Actavis LLC, USA and Abraxane 100 mg/vial (Albumin bound Paclitaxel 260 mg/m2) intravenous infusion Abraxis BioScience LLC, New Jersey in patients with metastatic breast cancer
100 项与 Actavis South Atlantic LLC 相关的临床结果
0 项与 Actavis South Atlantic LLC 相关的专利(医药)
100 项与 Actavis South Atlantic LLC 相关的药物交易
100 项与 Actavis South Atlantic LLC 相关的转化医学