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Bristol-Myers melanoma drug meets primary endpoint

Bristol-Myers Squibb Company has announced that a clinical trial of its investigational compound ipilimumab has met the primary endpoint of improving overall survival in previously-untreated patients with metastatic melanoma.

The study was designed to evaluate the overall survival in unresectable stage III or stage IV melanoma patients who have not received prior therapy.

The study compared ipilimumab 10mg/kg in combination with chemotherapy (dacarbazine) versus chemotherapy alone.

A regulatory filing for ipilimumab, based on a study known as 020, is currently under review by the US Food and Drug Administration and other health authorities around the world.

Study 020 assessed the overall survival in previously-treated unresectable stage III or stage IV melanoma patients, and it compared ipilimumab 3 mg/kg + gp100 vaccine, gp100 vaccine alone + ipilimumab alone, and gp100 vaccine alone.