• Mashup Score: 1

    The FDA has approved olutasidenib (Rezlidhia) capsules for adult patients with relapsed or refractory acute myeloid leukemia with a susceptible IDH1 mutation as detected by an FDA-approved test.

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    • ICYMI: The FDA has approved olutasidenib (Rezlidhia) capsules for adult patients with relapsed or refractory acute myeloid leukemia with a susceptible IDH1 mutation as detected by an FDA-approved test. #fdaapproved #oncology #leusm https://t.co/PSZ5Zp2vPb

  • Mashup Score: 7

    The FDA has granted accelerated approval to teclistamab-cqyv (Tecvayli) for adult patients with relapsed or refractory multiple myeloma who have received at least 4 previous lines of therapy, including a proteasome inhibitor, an immunomodulatory agent, and an anti-CD38 monoclonal antibody.

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    • BREAKING: @US_FDA Approves Teclistamab-cqyv for Relapsed or Refractory Multiple Myeloma #mmsm #FDAApproved #oncology https://t.co/gkXYeGEsMb https://t.co/dmzCFjN8t5

  • Mashup Score: 0

    The FDA approved eflapegrastim-xnst injection to reduce incidence of infection, as manifested by febrile neutropenia, in adults with nonmyeloid malignancies taking certain anticancer drugs, according to a company-issued press release.The approval of eflapegrastim-xnst (Spectrum Pharmaceuticals), a long-active granulocyte colony-stimulating factor with a novel formulation, applies to patients who

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    • .@US_FDA approves Rolvedon to reduce infection incidence among adults taking certain anticancer drugs. https://t.co/T18SlCickD #FDAApproved #MedEd #MedEducation #MedTwitter #OncoAlert @sppirx

  • Mashup Score: 0

    PODCAST Ophthalmology Journal dives deep into research articles, editorials, and more from the American Academy of Ophthalmology’s journal family: Ophthalmology, Ophthalmology Retina, Ophthalmology Glaucoma, and Ophthalmology Science. Join our rotating hosts of social media editors every other Thursday as they interview authors and editors about their groundbreaking…

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    • New #OphthalmologyJournal #Podcast! @DrLorraineEyeMD interviews Michael Snyder on the #FDAapproved #CustomFlex Artificial #Iris device https://t.co/rs9xvIbS7T https://t.co/b3BloblmmY