February 16, 2019


FDA Approves Large-Scale Commercial Production of Andexxa
Jennifer Barrett, Associate Editor
Andexxa (coagulation factor Xa [recombinant], inactivated-zhzo) was previously launched under an Early Supply Program with Generation 1 product. 
FDA Approves Dasatinib Approved for Pediatric Lymphoblastic Leukemia
Gina Columbus
Sprycel plus chemotherapy demonstrated a three-year event-free survival benefit during clinical trials.
Breast Cancer Biosimilar Gets FDA Approval
Jennifer Barrett, Associate Editor
The FDA approved trastuzumab-pkrb (Herzuma, Celltrion) as a biosimilar to Herceptin for the treatment of HER2-overexpressing breast cancer. 
Research Highlights Long-Term Efficacy of PCSK9 Inhibitor
Jennifer Barrett, Associate Editor
Evolocumab is approved as an adjunct to diet and other LDL cholesterol-lowering therapies in patients with primary hyperlipidemia and homozygous familial hypercholesterolemia.
Novel Triple Therapy Combination Shows Promise for Relapsed, Refractory Acute Myeloid Leukemia
Jennifer Barrett, Associate Editor
Overall response rate and survival in patients with relapsed AML treated with azacitidine plus nivolumab and ipilimumab may be superior to azacitidine plus nivolumab.
About the Specialty Pharmacy Times Industry Guide

The Specialty Pharmacy Times Industry Guide includes comprehensive editorial content relative to all specialty pharmacy stakeholders. Content includes information relative to market trends, commercialization, distribution, order to cash, HUB Services, managed care strategies and DIR fees. The guide also includes profiles, and a complete list of stakeholders along the patient journey: specialty pharmacies, wholesaler distributors, manufacturers, support services, group purchasing, and trade associations.

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