Gilead hit with FDA clinical hold for batch of HIV trials
The US Food and Drug Administration (FDA) has placed a clinical hold on several of Gilead’s trials evaluating two HIV …
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NHS to receive £29bn funding boost
The UK’s National Health Service (NHS) is receiving a £29bn ($39.1bn) funding boost, reflecting a 3% annual rise on current …
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Echosens and Boehringer expand partnership for MASH diagnosis
Echosens and Boehringer Ingelheim have expanded their collaboration aimed at expediting progress in metabolic dysfunction-associated steatohepatitis (MASH) diagnosis and care. The …
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Trump’s push to onshore pharma manufacturing clouded by ‘lack of clarity’
A degree of uncertainty reigns over the implementation of regulations imposed by US President Donald Trump that aim to bolster …
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Antares Therapeutics gains $177m for cancer medicines development
Antares Therapeutics has secured $177m in a Series A financing round for the development of precision medicines to treat cancer …
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Outlook’s wet AMD treatment accepted by SMC for NHS Scotland
The Scottish Medicines Consortium (SMC) has accepted Outlook Therapeutics’ Lytenava (bevacizumab gamma) for the treatment of wet age-related macular degeneration (wet …
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Odyssey bails on public listing as US IPO landscape stutters
Odyssey Therapeutics is unlikely to join the 2025 class of biotechs hitting the stock exchanges after the company withdrew its …
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Mosanna Therapeutics gains $80m to advance OSA nasal spray
Mosanna Therapeutics has secured $80m in a Series A funding round to advance a new nighttime nasal spray for obstructive …
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RFK Jr axes vaccine advisory committee members
The US department of Health and Human Services (HHS) has culled the 17 Biden-appointed members on the Advisory Committee for …
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MSD receives FDA approval for Enflonsia to prevent RSV
MSD has received US Food and Drug Administration (FDA) approval for Enflonsia (clesrovimab-cfor) to prevent respiratory syncytial virus (RSV) lower …
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EC approves Alnylam’s vutrisiran for ATTR-CM treatment
The European Commission (EC) has approved Alnylam Pharmaceuticals' Amvuttra (vutrisiran) to treat wild-type or hereditary transthyretin amyloidosis with cardiomyopathy (ATTR-CM) in adults. Amvuttra …
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FDA approves YolTech’s YOLT-101 for familial hypercholesterolemia
YolTech Therapeutics has received the US Food and Drug Administration (FDA) approval for its investigational new drug (IND) application for …
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Podcast: AI and Supervised Machine Learning in Clinical Trials – Part 2
In episode two of The Zelta Podcast, we continue our conversation about AI and supervised machine learning in clinical trials …
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Aytu BioPharma to commercialise Exxua for MDD in the US
Aytu BioPharma has signed an exclusive agreement with Fabre-Kramer Pharmaceuticals to commercialise Exxua (gepirone) extended-release tablets, a new antidepressant, to …
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American Society of Clinical Oncology (ASCO) Annual Meeting 2025
The American Society of Clinical Oncology (ASCO) Annual Meeting 2025, held from 30 May to 3 June, in Chicago, Illinois, …
