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Novartis partners with small North Carolina biotech to make its biologics...

Novartis announced a collaboration on Wednesday with a small North Carolina biotech whose technology could help turn more of the Swiss pharma giant’s infused drugs into injections that patients can...

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Novartis seeks to expand Leqvio into heart disease prevention

Novartis announced Wednesday that Leqvio lowered bad cholesterol levels, compared with a placebo or the cholesterol-lowering drug ezetimibe, in patients at low-to-moderate risk of developing...

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SpringWorks gets priority review; Botox competitor data; Hyundai's Covid...

SpringWorks scores FDA priority review: The agency accepted mirdametinib’s new drug application and granted it a priority review for the treatment of adult and pediatric patients with neurofibromatosis...

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FDA warns EyePoint over eye implant manufacturing woes

The FDA has sent EyePoint Pharmaceuticals a warning letter after uncovering manufacturing issues with the company’s eye implant Yutiq. The letter, issued July 12 and published Tuesday, said FDA...

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Sanofi pauses supply of two flu vaccines in China over ‘unexpected...

Sanofi is halting distribution of its two approved flu shots in China due to low potency, and says it won’t meet supply expectations for the products there this flu season. After what it called a...

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House Oversight chair tells PBM CEOs to correct testimonies from July hearing

House Oversight Chair James Comer (R-KY) has told the CEOs of the three major PBMs — CVS Caremark, Express Scripts and Optum Rx — to correct what he’s claiming are contradictions in their statements...

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Regeneron sues Sandoz to halt biosimilar to its blockbuster eye drug

Regeneron is going after Sandoz in a New Jersey federal court over Sandoz’s recently-approved drug Enzeevu, a biosimilar to Regeneron’s blockbuster eye treatment Eylea. Eylea, which has collected...

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Delaware high court to review expert testimony in Zantac suits, in win for...

Ten of the plaintiff-chosen experts expected to testify in litigation over whether the heartburn drug Zantac caused cancer will be reviewed by the Delaware Supreme Court, raising the possibility that...

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UK government partners with pharma on new £400M life science infusion

The new UK Labour government is making one of its first major investments in the biopharma ecosystem, establishing 18 new clinical trial hubs in a joint industry collaboration worth up to £400 million...

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How an upstart pharmacy benefit manager has been winning over companies like...

(This story is from our new Health Tech newsletter. If you’d like to sign up, just click here.)   In a market long dominated by three giants, a different kind of pharmacy benefit manager has been...

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BioMarin lays off 225 employees as it cuts spending on gene therapy rollout

BioMarin’s decision to scale back its gene therapy ambitions will result in about 225 employees losing their jobs, the biotech disclosed late Wednesday. The layoffs, which are tied to “organizational...

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Preclinical team hit hardest in Repare's R&D prioritization, layoffs

Repare Therapeutics is cutting its headcount by about 25%, with most of the layoffs concentrated in the company’s preclinical team, as part of what the company is calling a “strategic prioritization”...

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Merck ends two Phase 3 studies of Keytruda, including an early-stage...

Merck said Thursday morning it is discontinuing two Phase 3 trials of Keytruda, the world’s top-selling medicine, after independent data monitoring committees determined they weren’t going to succeed....

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J&J heads to FDA for Vyvgart competitor; Tokyo conglomerate launches venture...

Johnson & Johnson submits FDA application for Vyvgart competitor: The pharma company is seeking approval of nipocalimab in the autoimmune disease generalized myasthenia gravis, where argenx’s...

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Recursion nears ‘moment of truth’ with first key data, kicking off 18-month...

After years of talking up artificial intelligence’s potential to help make drugs, Recursion will finally bring data to the table — and lots of it. Sometime next month, the Salt Lake City-based biotech...

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Ahead of acquisition by Novo Holdings, are Catalent’s dark days behind it? 

In the months leading up to its pending acquisition by Novo Holdings, Catalent has meaningfully boosted its revenue for the first time in over a year, making headway while other contract manufacturers...

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Afrigen, CEPI to speed up mRNA vaccine manufacturing; Bora Pharma invests in...

Welcome to Endpoints News’ manufacturing briefs, where we bring you essential news on new builds, collaborations, recalls and more. The Coalition for Epidemic Preparedness Innovations (CEPI) is...

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FDA hints at what Chevron's elimination means in new SCOTUS filing

Earlier this summer, when the Supreme Court eliminated a longstanding legal doctrine that deferred to federal agencies on interpreting federal law, many legal observers said the move could spell the...

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Pennsylvania judge sides with drugmakers on first steps for growing GLP-1...

A Pennsylvania federal judge has agreed to prioritize two main arguments at issue in a growing number of lawsuits over the alleged side effects of GLP-1s, a legal decision that developers of the drugs...

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FDA’s drug evaluation wing launches new AI oversight panel

The FDA is hoping that rapidly-advancing artificial intelligence capabilities will not pass it by. The agency’s Center for Drug Evaluation and Research (CDER) has launched its own AI Council, according...

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