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U.S. Food and Drug Administration approves Pharmacyclics Inc's IMBRUVICA

Wednesday, 12 Feb 2014 01:18pm EST 

Pharmacyclics Inc:Says that the U.S. Food and Drug Administration (FDA) has approved IMBRUVICA (ibrutinib) as a single agent for the treatment of patients with chronic lymphocytic leukemia (CLL) who have received at least one prior therapy.This indication is based on overall response rate (ORR). An improvement in survival or disease-related symptoms has not been established.Says 1IMBRUVICA is the first once-daily, single-agent, oral kinase inhibitor for patients with CLL who have received one prior therapy1and is being jointly developed and commercialized by Pharmacyclics and Janssen Biotech, Inc. 

Company Quote

3.02 +2.48%
26 Dec 2014