Datopotamab deruxtecan new BLA submitted for accelerated approval in the US for patients with previously treated advanced EGFR mutated non-small cell lung cancer

12 November 2024 - Daiichi Sankyo and AstraZeneca’s new application is based on the TROPION-Lung05 Phase 2 trial and supported ...

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Unicycive Therapeutics announces US FDA acceptance of the new drug application for oxylanthanum carbonate for the treatment of hyperphosphataemia in patients with chronic kidney disease on dialysis

11 November 2024 - FDA sets PDUFA action date of 28 June 2025. ...

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Neurotech provides update on BLA for NT-501 as a treatment for macular telangiectasia type 2

8 November 2024 - Neurotech Pharmaceuticals today announced that the US FDA has extended the PDUFA goal date by three months ...

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Dizal submits new drug application to the US FDA for sunvozertinib in treating relapsed or refractory non-small cell lung cancer with EGFR exon 20 insertion mutations

8 November 2024 - The submission is supported by data from the pivotal WU-KONG1 Part B study, which featured in an ...

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Johnson & Johnson submits applications in the US and EU seeking approval of Darzalex Faspro/Darzalex as subcutaneous monotherapy for high risk smoldering multiple myeloma

8 November 2024 - If approved, Darzalex Faspro will become the first treatment option for patients with smoldering multiple myeloma at ...

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Satsuma Pharmaceuticals and SNBL resubmits the new drug application for STS101 (dihydroergotamine nasal powder) for the acute treatment of migraine with or without aura

30 October 2024 - Satsuma Pharmaceuticals and its corporate parent, Shin Nippon today announced the resubmission of the new drug ...

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Merus receives FDA extension of PDUFA for zenocutuzumab

5 November 2024 - Merus today announced that the US FDA has extended the PDUFA goal date for zenocutuzumab biologics ...

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Update on FDA review of Vtama (tapinarof) cream, 1% for the treatment of atopic dermatitis in adults and children 2 years of age and older

5 November 2024 - Organon today announced that the US FDA extended by three months the target action date of its ...

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Ionis announces FDA acceptance of new drug application for donidalorsen for prophylactic treatment of HAE

4 November 2024 - Donidalorsen PDUFA date set for 21 August 2025. ...

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Eisai completes rolling submission to US FDA for Leqembi (lecanemab-irmb) biologics license application for subcutaneous maintenance dosing for the treatment of early Alzheimer’s disease under the fast track status

31 October 2024 - Eisai and Biogen announced today that Eisai has completed the rolling submission of a biologics license application ...

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Verastem Oncology completes rolling NDA submission to the FDA for avutometinib plus defactinib as a treatment for recurrent KRAS mutant low grade serous ovarian cancer

31 October 2024 - Company seeking accelerated approval and priority review of its new drug application submission in patients with KRAS ...

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Abeona Therapeutics completes Pz-cel biologics license application resubmission to US FDA

29 October 2024 - Abeona Therapeutics today announced that the Company has resubmitted its biologics license application to the US FDA ...

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PTC Therapeutics announces FDA acceptance of Translarna NDA resubmission

30 October 2024 - PTC Therapeutics announced today the US FDA has accepted for review the resubmission of the new drug ...

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Foresee Pharmaceuticals announces submission of the NDA to the US FDA for the 3 month version of Camcevi for the treatment of advanced prostate cancer

30 October 2024 - Foresee Pharmaceuticals announced today that it has submitted a 505(b)(2) new drug application for the 3 month ...

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Lenz Therapeutics announces FDA acceptance of new drug application for LNZ100 for the treatment of presbyopia

21 October 2024 - FDA sets PDUFA target date of 8 August 2025. ...

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