Kiadis Pharma has said that the FDA has approved company's investigational new drug application to allow the start of a clinical phase III study for its product Reviroc in the US.
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Reviroc is under development for the elimination of cancer cells from an autologous graft in bone marrow transplantations for end-stage blood cancer patients. This approval follows the successful end of phase II meeting with the FDA for Reviroc and the subsequent submission of the IND package to the FDA.
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