Alfred Garfall, MD, discusses updated safety and efficacy data from a phase I trial evaluating teclistamab, a bispecific BCMA x CD3 antibody, for the treatment of patients with relapsed and/or refractory multiple myeloma.
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The U.S. Food and Drug Administration has lifted its full clinical hold on Protagonist Therapeutics’ clinical studies of rusfertide. The clinical hold was announced...
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In October, the U.S. Food and Drug Administration (FDA) held a workshop on the regulation of artificial intelligence (AI) in health care.
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White House Will Invest $100M in Addressing the Health Care Worker Shortage
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Current Issue
October 2021, Volume 7, Issue 12
This issue tells the long story of drug shortages, demystifies transfusion services, and more.