Belite Bio announces FDA granting of breakthrough therapy designation for tinlarebant for the treatment of Stargardt disease

21 May 2025 - Belite Bio today announced that the US FDA has granted breakthrough therapy designation for tinlarebant for ...

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FDA takes steps to enhance state importation programs to help lower prescription drug prices

21 May 2025 - The US FDA is continuing to take steps to help state importation programs provide safe, effective and ...

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Moderna provides update on BLA submission for combination vaccine against influenza and COVID-19

21 May 2025 -  Moderna today announced that in consultation with the US FDA, the Company has voluntarily withdrawn the ...

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US FDA grants approval for Jivi anti-hemophilic factor (recombinant), PEGylated-aucl in paediatric patients 7 to under 12 years of age with haemophilia A

19 May 2025 - Bayer announced that the US FDA has approved Jivi, a recombinant DNA-derived, extended half-life factor VIII ...

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US FDA approves BLA for Novavax's COVID-19 vaccine

19 May 2025 - Nuvaxovid is the only recombinant protein-based, non-mRNA COVID-19 vaccine available in the US. ...

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Zai Lab receives US FDA fast track designation for ZL-1310, a DLL3 targeted antibody drug conjugate, for treatment of extensive stage small cell lung cancer

19 May 2025 - The Company is on track to initiate a pivotal study for ZL-1310 in small cell lung ...

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FDA clears first blood test used in diagnosing Alzheimer’s disease

16 May 2025 - New test provides less invasive option, reduces reliance on PET scans and increases diagnosis accessibility. ...

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PharmaTher announces FDA extends review period for ketamine; new approval goal date 9 August 2025

16 May 2025 -  PharmaTher today announced the US FDA has extended the approval goal date for the review of ...

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Amneal receives US FDA approval for Brekiya (dihydroergotamine mesylate) injection for the acute treatment of migraine and cluster headaches in adults

15 May 2025 - Product will be available for appropriate patients in the second half of 2025 ...

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Kaerus Bioscience's lead candidate KER-0193 granted orphan drug designation and rare paediatric drug designation by US FDA for treatment of Fragile X syndrome

14 May 2025 - Kaerus Bioscience today announces that its lead candidate KER-0193 has been granted both orphan drug designation and ...

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FDA grants regenerative medicine advanced therapy designation for BrainChild Bio’s B7-H3 CAR T-cell therapy for incurable paediatric brain tumours

15 May 2025 - BrainChild Bio advancing BCB-276 towards BLA submission with a single pivotal Phase 2 trial planned to ...

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FDA approves retifanlimab-dlwr with carboplatin and paclitaxel and as a single agent for squamous cell carcinoma of the anal canal

15 May 2025 - Today, the FDA approved retifanlimab-dlwr (Zynyz, Incyte) with carboplatin and paclitaxel for the first-line treatment of ...

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FDA sets PDUFA date for Xspray Pharma’s re-submitted application for Dasynoc

14 May 2025 - The US FDA has acknowledged receipt of Xspray Pharma's re-submitted new drug application) for Dasynoc.  ...

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FDA extends PDUFA date of Biohaven's troriluzole NDA for rare disease spinocerebellar ataxia

14 May 2025 - Troriluzole would be the first and only FDA approved treatment for spinocerebellar ataxia, if approved. ...

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BioCryst announces FDA acceptance of NDA for Orladeyo (berotralstat) oral granules in patients with hereditary angioedema aged 2 to 11 years

14 May 2025 - FDA grants priority review of application, with PDUFA target action date of 12 September 2025. ...

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