FDA issues complete response letter for etripamil for PSVT

28 March 2025 - Complete response letter focused on CMC; no clinical issues relating to etripamil raised. ...

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FDA approves durvalumab for muscle invasive bladder cancer

28 March 2025 - Today, the FDA approved durvalumab (Imfinzi, AstraZeneca) with gemcitabine and cisplatin as neo-adjuvant treatment, followed by ...

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FDA approves novel treatment for haemophilia A or B, with or without factor inhibitors

28 March 2025 - Medication can be given up to once every 2 months. ...

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Fresenius receives FDA approval for their denosumab biosimilars and secures global settlement agreement

27 March 2025 - Conexxence (denosumab-bnht) and Bomyntra (denosumab-bnht) received FDA approval for all indications of the reference products: Prolia (denosumab) ...

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Soleno Therapeutics announces US FDA approval of Vykat XR to treat hyperphagia in Prader-Willi syndrome

26 March 2025 - First approved therapy to address hyperphagia in individuals with Prader-Willi syndrome. ...

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FDA approves cabozantinib for adults and paediatric patients 12 years of age and older with pNET and epNET

26 March 2025 - Today, the FDA approved cabozantinib (Cabometyx, Exelixis) for adult and paediatric patients 12 years of age ...

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Theratechnologies receives FDA approval for Egrifta WR (tesamorelin F8) to treat excess visceral abdominal fat in adults with HIV and lipodystrophy

25 March 2025 - New, improved formulation set to replace Egrifta SV. ...

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Blujepa (gepotidacin) approved by US FDA for treatment of uncomplicated urinary tract infections in female adults and paediatric patients 12 years of age and older

25 March 2025 - Blujepa is the first in a new class of oral antibiotics for uUTIs in nearly 30 ...

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FDA approves new prostate cancer imaging agent Gozellix

21 March 2025 - Telix Pharmaceuticals today announces that the US FDA has approved its new drug application for Gozellix ...

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Novartis receives third FDA approval for oral Fabhalta (iptacopan) – the first and only treatment approved in C3 glomerulopathy

20 March 2025 - Phase 3 study showed sustained proteinuria reduction at one year with favourable safety. ...

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Alnylam announces FDA approval of Amvuttra (vutrisiran), the first RNAi therapeutic to reduce cardiovascular death, hospitalisations and urgent heart failure visits in adults with ATTR amyloidosis with cardiomyopathy

20 March 2025 - Only therapeutic approved in the US to address both cardiomyopathy and polyneuropathy manifestations of ATTR amyloidosis. ...

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US FDA approves Tremfya (guselkumab), the first and only IL-23 inhibitor offering both subcutaneous and intravenous induction options, for adult patients with moderately to severely active Crohn’s disease

20 March 2025 - Supported by data from the GALAXI study, Tremfya is the only IL-23 inhibitor to show superiority versus ...

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FDA approves pembrolizumab for HER2 positive gastric or gastro-oesophageal junction adenocarcinoma expressing PD-L1

19 March 2025 - Today, the FDA granted traditional approval to pembrolizumab (Keytruda, Merck) with trastuzumab, fluoropyrimidine- and platinum-containing chemotherapy ...

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Scienture announces the US FDA approval of its NDA for SCN-102 to be launched as Arbli (losartan potassium) 10 mg/mL oral suspension

18 March 2025 - Scienture is pleased to announce the US FDA has approved SCN-102 with the brand name Arbli (losartan ...

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ANI Pharmaceuticals announces FDA approval for expansion of Iluvien label

14 March 2025 - ANI plans to begin marketing Iluvien in the US under the combined label later this year. ...

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