BridgeBio submits NDA to FDA for BBP-418 for individuals living with LGMD2I/R9

30 March 2026 - Comprehensive submission includes interim Phase 3 FORTIFY data demonstrating BBP-418’s rapid, consistent treatment effect and favourable safety ...

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Praxis Precision Medicines announces FDA acceptance and priority review of new drug application for relutrigine in patients with SCN2A and SCN8A DEEs

30 March 2026 - Praxis Precision Medicines today announced that the US FDA has accepted for priority review its new ...

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Teva gains biosimilar momentum with US FDA approval of Ponlimsi (denosumab-adet) and dual filing acceptance for biosimilar candidate to Xolair (omalizumab)

30 March 2026 -  Teva Pharmaceutical Industries today announced three milestones in its biosimilar portfolio, demonstrating continued momentum in the ...

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FDA approves new high dose regimen of Spinraza (nusinersen) for spinal muscular atrophy

30 March 2026 - The approval was anchored on data from the pivotal DEVOTE study that investigated the efficacy and safety ...

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Zymeworks receives US FDA fast track designation for ZW191, a folate receptor alfa targeting antibody drug conjugate

30 March 2026 - Zymeworks today announced that the US FDA has granted fast track designation to ZW191, an antibody ...

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Elevar Therapeutics announces FDA acceptance for review of new drug application for lirafugratinib as second-line cholangiocarcinoma treatment

30 March 2026 - Elevar Therapeutics today announced that the US FDA has completed its filing review of the new drug ...

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Awiqli approved in the US, the first and only once weekly basal insulin treatment for adults with type 2 diabetes

27 March 2026 - Novo Nordisk expects to launch Awiqli nationwide in the US in the second half of 2026. ...

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MeiraGTx announces FDA breakthrough therapy designation for AAV2-hAQP1 for the treatment of grade 2 and grade 3 radiation-induced xerostomia

26 March 2026 - FDA granted breakthrough therapy designation for AAV2-hAQP1 for the treatment of Grade 2 and Grade 3 late ...

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FDA approves first gene therapy for severe leukocyte adhesion deficiency type I

26 March 2026 - The US FDA today approved Kresladi (marnetegragene autotemcel), the first gene therapy for the treatment of severe ...

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Triana Biomedicines’ TRI-611 granted US FDA fast track designation for treatment of ALK positive non-small cell lung cancer

25 March 2026 - Triana Biomedicines today announced that the US FDA granted fast track designation for TRI-611, an investigational molecular ...

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FDA approves drug to treat neurologic manifestations of Hunter syndrome

25 March 2026 - The US FDA approved Avlayah (tividenofusp alfa-eknm) to treat certain individuals with Hunter syndrome (mucopolysaccharidosis type II ...

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FDA approves relacorilant with nab-paclitaxel for platinum-resistant epithelial ovarian, fallopian tube, or primary peritoneal cancer

25 March 2026 - Today, the FDA approved relacorilant (Lifyorli, Corcept Therapeutics), a glucocorticoid receptor antagonist, in combination with nab-paclitaxel ...

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IntraBio announces submission of supplemental new drug application for levacetylleucine for ataxia-telangiectasia

20 March 2026 - IntraBio today announced the submission of a supplemental new drug application to the US FDA for ...

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Toward greater transparency at the FDA - now is the time to act

18 March 2026 - The US FDA has generally sought to uphold the highest standards of scientific rigour in its regulation ...

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Political influence ‘a serious problem’ for FDA under Trump, former commissioner says

19 March 2026 - Political influence ‘a serious problem’ for FDA under Trump, former commissioner says. ...

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