SNT-5505 awarded US FDA fast track designation

10 June 2025 - Syntara today announces that its lead candidate, SNT-5505, has been granted fast track designation by the ...

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Zepzelca (lurbinectedin) and atezolizumab (Tecentriq) combination granted US FDA priority review for first-line maintenance treatment of extensive-stage small cell lung cancer

10 June 2025 - Target action (PDUFA) date set for 7 October 2025. ...

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X4 Pharmaceuticals granted fast track designation for mavorixafor for the treatment of chronic neutropenia by US FDA

10 June 2025 - X4 Pharmaceuticals today announced that the US FDA has granted fast track designation to mavorixafor, an oral ...

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Axsome Therapeutics provides update on the new drug application for AXS-14 for the management of fibromyalgia

9 June 2025 - Axsome Therapeutics today announced it has received a refusal to file letter from the US FDA ...

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Alnylam receives European Commission approval for Amvuttra (vutrisiran) for the treatment of ATTR amyloidosis with cardiomyopathy

9 June 2025 - Decision follows recent authorisations in the US and Brazil. ...

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US FDA approves Merck’s Enflonsia (clesrovimab-cfor) for prevention of respiratory syncytial virus lower respiratory tract disease in infants born during or entering their first RSV season

9 June 2025 - Enflonsia is the first and only RSV preventive option administered to infants using the same dose ...

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Lipocine announces filing of new drug submission for Tlando in Canada

9 June 2025  - New drug submission filed by Lipocine's licensing partner Verity Pharma. ...

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George Medicines announces FDA approval of Widaplik (telmisartan, amlodipine and indapamide), a new single pill combination treatment for hypertension in adults, including initial treatment

9 June 2025 - Commercialisation planning underway with US launch anticipated Q4, 2025. ...

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European Commission approves Duvyzat for the treatment of Duchenne muscular dystrophy

6 June 2025 - The approval is based on Phase 3 EPIDYS trial data that demonstrated meaningful treatment benefits in ambulant ...

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Arvinas announces submission of new drug application to US FDA for vepdegestrant for patients with ESR1 mutated ER+/HER2- advanced or metastatic breast cancer

6 June 2025 - Arvinas today announced the submission of a new drug application to the US FDA with its partner ...

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Fixed-duration Calquence-based regimens approved in EU for patients with chronic lymphocytic leukaemia in the first-line setting

6 June 2025 - AMPLIFY Phase III trial results demonstrated statistically significant and clinically meaningful improvement in progression-free survival for ...

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Merz Aesthetics receives approval from Health Canada for Radiesse as an aesthetic injectable for the treatment of moderate wrinkles in the décolleté area

5 June 2025 - Merz Aesthetics Canada announced today the Health Canada approval for Radiesse for the treatment of moderate ...

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Sydnexis announces European Commission approval of SYD-101, the first and only pharmaceutical treatment for slowing the progression of paediatric myopia

5 June 2025 - Exclusive licensing partner Santen will commercialise SYD-101 under the brand name Ryjunea in the EU. ...

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Linerixibat new drug application accepted for review by the US FDA for cholestatic pruritus in patients with primary biliary cholangitis

2 June 2025 - GSK today announced the US FDA has accepted for review the new drug application for linerixibat, an ...

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TGA approves weight loss drug to treat sleep disorder

4 June 2025 - The country’s medicines regulator has approved the use of a GLP-1 weight-loss drug to treat people ...

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