Jiangsu to ‘reapply for US approval of rivoceranib combo therapy ASAP’

23 May 2024 - Hangseo Hengrui Pharmaceuticals said Thursday that it would meet with the US FDA as soon as ...

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Atara Biotherapeutics submits tabalecleucel (tab-cel) biologics license application for treatment of Epstein-Barr virus positive post-transplant lymphoproliferative disease with US FDA

20 May 2024 - First allogeneic T-cell therapy BLA submission to US FDA. ...

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OWP Pharmaceuticals announces FDA filing acceptance for new drug application of Subvenite (lamotrigine) oral suspension

20 May 2024 - OWP announced today that it has received US FDA acceptance for the new drug application submission ...

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Durect Corporation receives FDA breakthrough therapy designation for larsucosterol in alcohol-associated hepatitis

21 May 2024 - Durect plans to confirm the efficacy and safety of larsucosterol in a registrational Phase 3 clinical ...

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Bristol Myers Squibb announces updated action date by the US FDA for subcutaneous nivolumab (nivolumab and hyaluronidase)

21 May 2024 - Updated PDUFA goal date of 29 December 2024. ...

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Axogen initiates rolling submission of biologics license application to US FDA for Avance Nerve Graft

16 May 2024 - Axogen is pleased to announce that it has initiated the rolling submission process with the US FDA ...

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Dynavax provides regulatory update on sBLA for four dose Heplisav-B regimen for adults on haemodialysis in the US

14 May 2024 - Dynavax Technologies today provided a regulatory update for the Company's supplemental biologics license application to include ...

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Ascendis Pharma announces extension of US FDA review period for TransCon PTH for adults with hypoparathyroidism

14 May 2024 - PDUFA goal date extended by three months for further review of submission to 14 August 2024. ...

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Eisai initiates rolling biologics license application to US FDA for Leqembi (lecanemab-irmb) for subcutaneous maintenance dosing

15 May 2024 - BioArctic's partner Eisai announced today that they have initiated the rolling submission of a biologics license application ...

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PTC Therapeutics announces FDA acceptance and priority review of the BLA for Upstaza

14 May 2024 - PDUFA target action date of 13 November 2024. ...

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Sumitomo Pharma announces FDA acceptance of supplemental new drug application for vibegron in men with overactive bladder symptoms receiving pharmacological therapy for benign prostatic hyperplasia

13 May 2024 - Supplemental new drug application submission based on Phase 3 study of vibegron 75 mg (Gemtesa) demonstrating statistically ...

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Dupixent (dupilumab) sBLA accepted for FDA priority review for treatment of adolescents with chronic rhinosinusitis with nasal polyposis

13 May 2024 - If approved, Dupixent would be the first treatment in the US indicated for adolescents aged 12-17 years ...

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Moderna announces update on investigational RSV vaccine

10 May 2024 - US FDA has informed Moderna that due to administrative constraints, the agency will not complete its review ...

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Merus announces US FDA acceptance and priority review of biologics license application for zenocutuzumab for the treatment of NRG1 positive NSCLC and PDAC

6 May 2024 - If approved, zenocutuzumab will be the first targeted therapy for NRG1 positive cancer. ...

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US FDA accepts Bristol Myers Squibb’s application for subcutaneous nivolumab (nivolumab and hyaluronidase)

6 May 2024 - Application based on results from CheckMate-67T, the first Phase 3 trial of the subcutaneous formulation of nivolumab ...

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