February 16, 2019


Cablivi Gets FDA Approval for Rare Blood Clotting Disorder
Jennifer Barrett, Associate Editor
Caplacizumab-yhdp treats adults with acquired thrombotic thrombocytopenic purpura, a rare and life-threatening blood clotting autoimmune disorder.  
FDA Expands Alimta Label With Keytruda for Front Line Treatment of Non-Small Cell Lung Cancer
Jennifer Barrett, Associate Editor
Pemetrexed plus pembrolizumab is indicated for use along with platinum chemotherapy for the first-line treatment of patients with metastatic nonsquamous non-small cell lung cancer with no EGFR or ALK genomic tumor aberrations.
Rituximab Biosimilar Shows Equivalent Efficacy in Clinical Trials
Cecilia Pessoa Gingerich
There is currently no rituximab biosimilar approved by the FDA for rheumatoid arthritis.
Herceptin Biosimilar Gets FDA Approval
SPT Staff
Ontruzant (trastuzumab-dttb) is indicated for the treatment of HER2-positive breast cancer and HER2 overexpressing gastric cancer.
Sickle Cell Disease Drug Gets FDA Breakthrough Designation
Jennifer Barrett, Associate Editor
Crizanlizumab under evaluation for the prevention of vaso-occlusive crises in patients of all genotypes with sickle cell disease.
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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