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Anemia

FDA clears study of HEMOLINK as a treatment for chemotherapy-induced anemia

Published in Blood Weekly, May 2nd, 2002

Hemosol, Inc., (HMSL) announced that it has received clearance from the U.S. Food and Drug Administration (FDA) to begin a phase II clinical trial of its flagship product, Hemolink (hemoglobin raffimer), as a treatment for chemotherapy-induced anemia.

The single-blind, dose-comparison study will evaluate the safety and tolerability of a short course of HEMOLINK in 50 patients with lung or ovarian cancer who are being treated with erythropoietin for chemotherapy-induced anemia. The multicenter study will be led by investigators at Duke University and is expected to begin enrolling patients in June of 2002.

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