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A major milestone for the Primary Immunodeficiency community: the FDA approval of Rocket Pharmaceuticals' KRESLADI™, marking an important advancement for children living with severe Leukocyte Adhesion Deficiency-I (LAD-I). This innovative gene therapy represents meaningful progress toward addressing the underlying cause of disease — offering new hope for improved outcomes and quality of life. We’re also proud to share that Vanessa Tenembaum, CEO of the Jeffrey Modell Foundation, was featured in the announcement, noting: “The approval of KRESLADI represents a significant development for individuals affected by severe LAD-I and the broader primary immunodeficiency community.” At JMF, we remain committed to advancing research, early diagnosis, and access to life-changing treatments for patients worldwide. 👩‍💻 Read the full press release here: bit.ly/4va2Fdq #PrimaryImmunodeficiency #GeneTherapy #LADI #MedicalInnovation #FDApproval #Immunology #PatientAdvocacy #GlobalHealth #JeffreyModellFoundation
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4 Sep 2025
We’re thrilled to announce FDA approval for the Globe® Pulsed Field System, our groundbreaking solution for treating atrial fibrillation. Welcome to the future of integrated mapping and ablation. bit.ly/4g0aOtq #FDApproval #EPeeps x.com/KardiumInc/status/1963…
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A lot of people are not getting vaxed because it hasn't been tested long enough. Y'all keep making it political:for us it's NOT. I was in R&D for 10 yrs. The issue of testing any drug for just 1 yr & then MANDATING everyone take this exp'mental drug. FDApproval takes 3-5 yrs MIN.
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In the urgent context of medical cures, three-week approval cycle wasn’t sustainable. Implementing new digital policy procedures that take place “where the work happens” reduced approval cycles from 21-days to just three. Via @kpodnar 👇 #fdapproval simplea.com/Articles/improvi…

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In the urgent context of medical cures, three-week approval cycle wasn’t sustainable. Implementing new digital policy procedures that take place “where the work happens” reduced approval cycles from 21-days to just three. Via @kpodnar 👇 #fdapproval simplea.com/Articles/improvi…

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The @US_FDA granted accelerated approval to #Blenrep @GSKUS for adults with relapsed or refractory multiple myeloma. pharmacypracticenews.com/FDA… @SagarLonialMD @WinshipAtEmory #FDA #fdapproval #myeloma

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The @US_FDA approved a smartphone app that links @AbbottNews #neuromodulation devices to a variety of @Apple products. painmedicinenews.com/Online-… @UToledo @BoettigerKeith #chronicpain #fda #fdapproval

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