FDA approves Arcutis’ Zoryve (roflumilast) cream 0.05% for the treatment of atopic dermatitis in children ages 2 to 5

6 October 2025 - Commercial product expected to be available by the end of October 2025. ...

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Spruce Biosciences receives US FDA breakthrough therapy designation for tralesinidase alfa enzyme replacement therapy in Sanfilippo syndrome type B

6 October 2025 - Breakthrough therapy designation supported by integrated long-term clinical data demonstrating normalisation in cerebral spinal fluid heparan sulphate ...

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EG 427 receives US FDA fast track designation for EG110A DNA medicine in neurogenic bladder patients

6 October 2025 - EG 427 announced today that the US FDA granted fast track designation to EG110A, its novel DNA ...

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Amgen makes Repatha available though AmgenNow, a direct to patient program in the US

6 October 2025 - Eligible patients can access Repatha at nearly 60% discount from the list price. ...

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Why Pfizer’s Trump deal is good news for all of big pharma

2 October 2025 - The company’s accord with the president clears a cloud over the whole sector. ...

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Alzinova receives fast track designation from US FDA for ALZ-101 in Alzheimer’s disease

4 October 2025 - Alzinova today announces that the US FDA has granted fast track designation for the company’s vaccine candidate ...

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Ensem Therapeutics announces ETX-636 granted fast track designation by the FDA for advanced breast cancer

1 October 2025 - Ensem Therapeutics today announced the US FDA granted fast track designation to its clinical stage pan mutant-specific ...

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Does big pharma gouge Americans?

2 October 2025 - In the bloated health care system, others are the real money makers. ...

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FDA approves Roche’s Tecentriq plus lurbinectedin as first-line maintenance therapy for extensive-stage small cell lung cancer

3 October 2025 - Regimen recommended in National Comprehensive Cancer Network Guidelines for small cell lung cancer. ...

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Nacuity Pharmaceuticals granted US FDA breakthrough therapy designation for NPI-001 (N-acetylcysteine amide) tablets for the treatment of retinitis pigmentosa

2 October 2025 - Nacuity Pharmaceuticals today announced that the US FDA has granted breakthrough therapy designation to NPI-001 (N-acetylcysteine amide) ...

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FDA approves lurbinectedin in combination with atezolizumab or atezolizumab and hyaluronidase-tqjs for extensive-stage small cell lung cancer

2 October 2025 - Today, the FDA approved lurbinectedin (Zepzelca, Jazz Pharmaceuticals) in combination with atezolizumab (Tecentriq) or atezolizumab and ...

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Taysha Gene Therapies announces FDA breakthrough therapy designation and provides positive regulatory update on TSHA-102 in Rett syndrome

2 October 2025 - Breakthrough therapy designation granted based on FDA’s review of available clinical evidence of safety and efficacy from ...

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Calico Life Sciences announces US FDA fast track designation for investigational treatment of autosomal dominant polycystic kidney disease

2 October 2025 - Calico Life Sciences today announced the US FDA granted fast track designation for ABBV-CLS-628, an investigational therapy ...

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Wockhardt submits new drug application to US FDA for zidebactam-cefepime (WCK 5222) for treatment of serious gram-negative infections

1 October 2025 - Wockhardt today announced the submission of new drug application to the US FDA for its novel ...

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TAHO Pharma announces submission of new drug application to the US FDA for TAH3311 – the world’s first apixaban oral dissolving film – represents a transformational advancement in anti-coagulant therapy

30 September 2025 - TAHO Pharmaceuticals today announced the submission of its new drug application to the US FDA for TAH3311, ...

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