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CollaGenex seeks UK approval for Oracea

The marketing authorization application (MAA) was based primarily upon safety and efficacy results from two phase III clinical trials for Oracea. In the two studies, patients receiving Oracea

ViroPharma to develop C difficile treatment

ViroPharma plans to initially focus its efforts on the opportunity to prevent recurrence of clostridium difficile-associated disease (CDAD) following treatment with Vancocin. The company is currently conducting feasibility

Genitope initiates MyVax leukemia trial

MyVax personalized immunotherapy is based on the unique genetic makeup of a patient’s own tumor, and is designed to activate the patient’s immune system to fight cancer. Nine