Aldeyra Therapeutics announces PDUFA extension of the new drug application of reproxalap for the treatment of dry eye disease

15 December 2025 - Aldeyra Therapeutics today announced that the US FDA has extended the PDUFA target action date for the ...

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Leo Pharma submits adolescent label expansion application for Anzupgo to EMA

15 December 2025 - Leo Pharma today announced submission of a label expansion application to the EMA to expand the ...

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US FDA approves LIB Therapeutics’ Lerochol (lerodalcibep-liga) for adults with elevated LDL-cholesterol

15 December 2025 - Lerochol expected to be available in the US in spring 2026. ...

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Sentynl Therapeutics announces FDA acceptance of CUTX-101 NDA resubmission

15 December 2025 - Sentynl Therapeutics today announced that the US FDA has accepted the resubmission of its new drug ...

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Tris Pharma announces FDA acceptance of NDA for once nightly, low sodium oxybate product for narcolepsy and idiopathic hypersomnia

9 December 2025 - Tris Pharma today announced that the US FDA has accepted the company’s new drug application for TRN-257 ...

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US FDA grants priority review to Bristol Myers Squibb's application for Opdivo (nivolumab) plus chemotherapy combination for classical Hodgkin's lymphoma

11 December 2025 - Bristol Myers Squibb today announced that the US FDA has accepted and granted priority review to ...

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Agios provides update on US sNDA for mitapivat in thalassaemia

8 December 2025 - Agios Pharmaceuticals today announced that the US FDA has not yet issued a regulatory decision on the ...

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Baxdrostat new drug application accepted under FDA priority review in the US for patients with hard to control hypertension

2 December 2025 - Submission based on positive BaxHTN Phase 3 trial results which demonstrated statistically significant and clinically meaningful reduction ...

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MannKind announces US FDA accepts for review its supplemental new drug application of Furoscix ReadyFlow Auto-injector for the treatment of oedema in adults with chronic heart failure or chronic kidney disease

1 December 2025 - MannKind Corporation today announced that the US FDA has accepted the sNDA seeking approval for Furoscix ReadyFlow ...

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EMA validates type II variation application for Padcev (enfortumab vedotin) with Keytruda (pembrolizumab) for certain patients with muscle-invasive bladder cancer

1 December 2025 - Astellas Pharma today announced that the EMA validated for review a type II variation application for ...

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Merck granted fast track designation by the US FDA for MK-2214 for the treatment of Alzheimer's disease

1 December 2025 - MK-2214, an investigational novel antibody targeting phosphorylated serine 413 (pS413) tau. ...

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Vanda Pharmaceuticals provides regulatory update on tradipitant for motion sickness

28 November 2025 - Vanda Pharmaceuticals today announced updates regarding tradipitant for motion sickness. ...

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US FDA grants priority review to sonrotoclax for the treatment of relapsed or refractory mantle cell lymphoma

26 November 2025 - BeOne Medicines today announced that the US FDA has accepted and granted priority review to a ...

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Novo Nordisk files for FDA approval of a higher dose of Wegovy injection 7.2 mg

26 November 2025 - Today, Novo Nordisk announced the submission of an supplemental new drug application to the US FDA ...

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Ascendis announces extension of FDA review period for TransCon CNP (navepegritide) for children with achondroplasia

25 November 2025 - PDUFA goal date extended by three months to 28 February 2026. ...

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