Moderna receives full US FDA approval for COVID-19 vaccine, Spikevax, in children aged 6 months through 11 years at increased risk for COVID-19 disease

10 July 2025 - Spikevax is now approved for all adults aged 65 years and older, and individuals aged 6 ...

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Bayer files for EU approval of gadoquatrane

10 July 2025 - Submission of marketing authorization application to the EMA seeking approval for investigational low dose gadoquatrane for contrast-enhanced ...

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European Commission approves Tevimbra in combination with chemotherapy as a first-line treatment for nasopharyngeal carcinoma

10 July 2025 - New indication based on results of RATIONALE-309 study demonstrating statistically significant improvement in progression-free survival. ...

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Milestone Pharmaceuticals announces FDA acceptance of the company’s response to the CRL for Cardamyst (etripamil) nasal spray

11 July 2025 - New PDUFA action date of 13 December 2025. ...

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Ultragenyx receives complete response letter from FDA for UX111 AAV gene therapy to treat Sanfilippo syndrome type A

11 July 2025 - complete response letter cited specific chemistry, manufacturing and controls related observations that are resolvable. ...

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Swissmedic approves Ifinwil (eflornithine) for children diagnosed with high-risk neuroblastoma

8 July 2025 - Norgine is pleased to announce that Swissmedic has approved the registration of Ifinwil (eflornithine) as monotherapy ...

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Capricor Therapeutics provides regulatory update on deramiocel BLA for Duchenne muscular systrophy

11 July 2025 - Capricor plans to resubmit its BLA to include data from the ongoing Phase 3 HOPE-3 trial in ...

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MHRA approves elinzanetant to treat moderate to severe vasomotor symptoms (hot flushes) caused by menopause

8 July 2025 - The MHRA has today become the first regulator in the world to approve elinzanetant (Lynkuet) for the ...

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FDA approves updated label for Lilly's Kisunla (donanemab-azbt) with new dosing in early symptomatic Alzheimer's disease

9 July 2025 - The newly recommended dosing schedule significantly lowered ARIA-E rates compared to the original dosing schedule, adding ...

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KalVista Pharmaceuticals announces FDA Approval of Ekterly (sebetralstat), first and only oral on-demand treatment for hereditary angioedema

7 July 2025 - First new on demand hereditary angioedema treatment in over a decade, with potential to transform management of the ...

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MHRA approves nogapendekin alfa inbakicept to treat adult patients with non-muscle invasive bladder cancer 

4 July 2025 - The MHRA has today approved nogapendekin alfa inbakicept (Anktiva) for adults with BCG unresponsive non-muscle invasive bladder ...

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European Commission approves Biocon biologics’ denosumab biosimilars

3 July 2025 - Biocon Biologics today announced that the European Commission has granted marketing authorisation in the European Union ...

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Imfinzi approved in the EU as first and only peri-operative immunotherapy for muscle-invasive bladder cancer

4 July 2025 - Approval based on NIAGARA Phase III trial results which showed a 32% reduction in the risk ...

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Jazz Pharmaceuticals receives European Commission marketing authorisation for Ziihera (zanidatamab) for the treatment of advanced HER2 positive biliary tract cancer

1 July 2025 - Conditional approval based on positive results from the HERIZON-BTC-01 Phase 2b trial. ...

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Johnson & Johnson submits application to the EMA seeking indication extension of Akeega (niraparib and abiraterone acetate dual action tablet) for the treatment of adult patients with metastatic hormone-sensitive prostate cancer and HRR gene alterations

3 July 2025 - The submission is based on results from the Phase 3 AMPLITUDE study evaluating niraparib in combination with ...

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