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F2G inks $100M Series H for another shot at treating fungal infections

Manchester, UK-based F2G has patched together another $100 million in funding a little over a year after receiving a CRL for its experimental fungal infection drug known as olorofim, it said Thursday...

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Cancer gene therapy startup Vironexis emerges from stealth with $26M seed round

A new startup attempting to develop AAV gene therapies to treat cancer emerged from stealth Thursday morning with $26 million in seed funding — and a plan to quickly get into the clinic. Vironexis...

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Noom offers compounded GLP-1 drugs, promises patients can quit and keep...

(This story is from our new Health Tech newsletter. If you’d like to sign up, just click here.)  Noom is the latest weight loss startup to start prescribing compounded versions of the obesity...

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Gilead says twice-yearly HIV prevention shot succeeds in second pivotal trial

Gilead announced that its twice-a-year HIV injection prevented all but two cases of HIV among 2,180 participants in a Phase 3 study as it prepares to launch the drug, called lenacapavir, in 2025 for...

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Lilly budgets $1.8B to boost Kisunla, GLP-1 manufacturing in Ireland

Eli Lilly is rapidly increasing its presence in Ireland with a $1 billion expansion to bolster its biologic drug production and a separate $800 million investment to further grow its GLP-1...

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Sofinnova’s Jim Healy on ‘more rational market’ as four biotech startups near...

In what’s shaping up to be another slow year for biotech IPOs — better, however, than the 2022 and 2023 doldrums — Jim Healy is somewhat of an outlier. Only four biotechs from this year’s IPO class are...

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Charles River to lay off 3% of staffers as it streamlines spending

Charles River Laboratories is cutting around 3% of its total workforce in “response to current trends,” a company spokesperson told Endpoints News in an email. The Wilmington, MA-based company is...

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Fulcrum's Phase 3 for old GSK drug fails, stock sinks

Fulcrum Therapeutics reported a Phase 3 fail Thursday morning, sending its stock plummeting. The biotech said that a study testing the former GSK cardio drug losmapimod in facioscapulohumeral muscular...

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GSK’s mRNA flu shot is heading to Phase 3; Summit’s $235M offering

Plus, news about Oruka Therapeutics, Centessa, Takeda, Innate Pharma and Liquidia: GSK’s mRNA flu vaccine succeeds against both strains in Phase 2: The pharma company said the vaccine candidate...

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Debiopharm, ITM ink €300M licensing deal for cancer treatment

Debiopharm and ITM announced a licensing deal for a ​​radiopharmaceutical treatment that’s being investigated in several cancers. Andrew Cavey Debiopharm, which is based in Switzerland, is eligible for...

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Australian RNA manufacturer launches; Forge Biologics’ CEO steps down

Welcome to Endpoints News’ manufacturing briefs, where we bring you essential news on new builds, collaborations, recalls and more. A new RNA therapeutics manufacturing company based in Sydney,...

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FDA should embrace new ways of evaluating rare disease drugs, report argues

To increase the pace of rare disease drug approvals, the FDA should embrace nontraditional data, deploy new forms of analysis and be more open about its decisions, according to a new report from the...

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Avadel's narcolepsy drug Lumryz misses PDUFA date, still under review at FDA

Avadel Pharmaceuticals is still waiting on an answer from the FDA on whether its once-nightly narcolepsy drug Lumryz will be approved to include the pediatric population after the agency missed the...

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FDA revisits new structure for drug review documents, aiming to better...

Back in 2019, as part of a program focused on improving documentation and communications for drug approvals, the FDA made a change to how it explains its decisions. At the time, academics and industry...

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Seres' microbiome therapy reduces infections in stem cell transplant...

Seres Therapeutics, the biotech company that pioneered one of the first microbiome drugs, a pill containing bacterial spores purified from poop, announced promising but early results for a new...

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Roche’s Tecentriq scores first US approval for subcutaneous PD-1

Just in time for the first day of ESMO, the FDA has approved its first-ever subcutaneous immunotherapy targeting PD-1 for cancer. The new formulation of Roche’s Tecentriq — to be marketed as Tecentriq...

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Bicara, Zenas and MBX rekindle IPO market with rare Friday tripleheader

After a sleepy few months, the biotech IPO market is waking up thanks to back-to-back-to-back listings. Oncology-focused Bicara Therapeutics, autoimmune startup Zenas BioPharma and metabolic drug...

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Neurocrine culls Phase 2 neuropsych med after failing to validate earlier data

Neurocrine is halting further development of luvadaxistat after it failed to improve cognitive impairment in patients with schizophrenia in a mid-stage study. The company said in a Thursday update that...

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Oncternal stops cancer trials and begins search for future business options

After disappointing efficacy data and a patient death, Oncternal Therapeutics is discontinuing two trials and looking for strategic alternatives. The San Diego company said it would end a Phase 1 trial...

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Doug Williams returns with a ‘FIT’ bet on CAR-Ts; Biogen appoints Mene...

Doug Williams Industry veteran Doug Williams is back with a new approach to CAR-T cell therapies that he expects to take into the clinic in the US by year’s end. After a brief stint at Sana...

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