FDA Approves Revumenib as Therapy for Relapsed or Refractory AML
Pune, India | October 27, 2025 The U.S. Food and Drug Administration (FDA) recently approved revumenib, an innovative oral menin inhibitor, to treat relapsed or
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February 3, 2026
Pune, India | October 27, 2025 The U.S. Food and Drug Administration (FDA) recently approved revumenib, an innovative oral menin inhibitor, to treat relapsed or
Read MorePune, India | October 24, 2025 The recent U.S. Food and Drug Administration (FDA) approval of Blenrep (belantamab mafodotin-blmf) for adults with relapsed or refractory
Read MoreBy Mursalin Pathan – Content Writer Pune, India | October 20, 2025 Zynex, a prominent developer of non-invasive medical technologies, has received clearance from the
Read MorePune, India | October 07, 2025 The U.S. Food and Drug Administration (FDA) has officially approved a new maintenance therapy for adults with extensive-stage small
Read MorePune, India | October 03, 2025 The U.S. Food and Drug Administration (FDA) has approved Evkeeza® (evinacumab‑dgnb) for children as young as one year diagnosed
Read MorePune, India | August 26, 2025 Regeneron Pharmaceuticals received a Complete Response Letter (CRL) from the FDA that denied its request to expand the EYLEA HD®
Read MorePune, India | August 21, 2025 The U.S. Food and Drug Administration (FDA) has granted accelerated approval for a new targeted treatment that combines avutometinib
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