FDA Approves Acalabrutinib to Treat CLL/SLL
As part of Project Orbis, The FDA has approved acalabrutinib (Calquence) for the treatment of adult patients with chronic lymphocytic leukemia or small lymphocytic lymphoma.
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FDA Accepts Biologics License Application for Bevacizumab Biosimilar
The FDA has accepted a biologics license application (BLA) under the 351(k) pathway for SB8, a biosimilar candidate for bevacizumab (Avastin), according to Samsung Bioepis, the developer of the agent.
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IN CASE YOU MISSED IT
 
Patient-Reported Outcomes Bolster Breast Cancer Treatment
Survival of patients with metastatic breast cancer has improved substantially over recent decades, but a new study shows that there is substantial regional variation in survival and in the improvement in survival.
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