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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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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MHRA approves aumolertinib to treat non-small cell lung cancer

3 June 2025 - The MHRA has approved aumolertinib (Aumseqa) for adult patients with non-small cell lung cancer. ...

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European Commission approves Adcetris (brentuximab vedotin) for the treatment of adult patients with newly diagnosed stage IIb/III/IV Hodgkin lymphoma in combination with ECADD

3 June 2025 - Approval based on positive results from the Phase 3 HD21 trial for stage IIb with risk factors/III/IV ...

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FDA approves darolutamide for metastatic castration-sensitive prostate cancer

3 June 2025 - Today, the FDA approved darolutamide (Nubeqa) for metastatic castration-sensitive prostate cancer (mCSPC).  ...

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MaaT Pharma submits marketing authorisation application to the EMA for Xervyteg (MaaT013) in acute graft versus host disease

2 June 2025 - The marketing authorisation application submitted to the EMA is based on data from the Pivotal ARES study, evaluating ...

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Zealand Pharma submits marketing authorisation application to the EMA for glepaglutide in short bowel syndrome

2 June 2025 - Zealand Pharma today announced the submission of a marketing authorisation application to the EMA for glepaglutide, ...

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FDA accepts TransCon CNP NDA for priority review

2 June 2025 - Ascendis Pharma today announced that the US FDA has accepted for priority review its new drug application ...

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Kura Oncology and Kyowa Kirin announce FDA acceptance and priority review of new drug application for ziftomenib in adults with relapsed or refractory NPM1 mutant AML

1 June 2025 - New drug application based on positive results from the Phase 2 KOMET-001 trial. ...

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