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Pharma Industry News
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Business-News-Today.com section for global pharma industry news, Indian pharma sector latest news, pharma sector news today, pharmaceuticals industry news.
FDA approval and $12m funding propel Femasys’ FemBloc toward market-ready milestone
Discover how Femasys’ FemBloc advances with FDA clearance and $12 M in funding, propelling its non-surgical birth control toward commercialization.
Cogent Biosciences posts Q3 2025 results with $430m cash and pivotal trial momentum
Find out how Cogent Biosciences is using its $430 million cash runway and regulatory momentum to drive late-stage trials and pipeline expansion in 2025.
Eli Lilly (NYSE: LLY) to build $3bn Netherlands plant to power global obesity drug supply
Find out how Eli Lilly’s $3 billion Netherlands plant will reshape obesity drug manufacturing and strengthen Europe’s pharma supply chain resilience.
uniQure moves closer to FDA approval as AMT-130 gene therapy shows progress for Huntington’s disease
Find out how uniQure’s AMT-130 regulatory path for Huntington’s disease is evolving after the FDA’s latest feedback on its data sufficiency.
FDA lifts hold on Rein Therapeutics’ LTI-03 trial, reviving hopes for idiopathic pulmonary fibrosis treatment
FDA clears Rein Therapeutics to restart its Phase 2 trial of LTI-03 for idiopathic pulmonary fibrosis, restoring investor confidence and trial momentum.
Phio’s INTASYL therapy PH-762 shows 100% tumor clearance in skin cancer dose-escalation study
Find out how Phio Pharmaceuticals’ RNAi-based PH-762 achieved high tumor clearance in a skin cancer study and what it could mean for non-surgical treatment paths today!
HUTCHMED’s ATTC platform and fruquintinib combo data headline 2025 R&D updates
Find out how HUTCHMED’s new ATTC platform and strong late-stage trial results could reshape its cancer drug pipeline and investor outlook today.
Breakthrough hope: Benitec Biopharma’s BB-301 delivers promising results in rare muscular dystrophy trial
Find out how Benitec Biopharma’s BB-301 gene therapy is showing early success in restoring swallowing function for OPMD patients.
Belite Bio wins UK MHRA nod to file conditional marketing application for tinlarebant in Stargardt disease
Find out how Belite Bio gained UK MHRA backing to file a conditional marketing application for tinlarebant, advancing the first potential therapy for Stargardt disease.
FDA accepts Alvotech and Teva’s BLA for AVT05, advancing first golimumab biosimilar in the U.S.
FDA accepts Alvotech and Teva’s BLA for AVT05, a proposed golimumab biosimilar — find out how this milestone strengthens U.S. biosimilar competition.