SAN DIEGO, June 15 /PRNewswire-FirstCall/ -- Favrille, Inc. (Nasdaq: FVRL - News), a biopharmaceutical company developing patient-specific immunotherapies for the treatment of cancer, announced today that its electronic Investigational New Drug (IND) application for FAV-201, a patient-specific immunotherapy for the treatment of T-cell lymphoma, has been cleared by the U.S. Food & Drug Administration (FDA). Initially, FAV-201 will be evaluated in cutaneous T-cell lymphoma (CTCL).
