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AstraZeneca reveals early data for oral PCSK9, touts PK edge over Merck’s drug

AstraZeneca has unveiled the early efficacy profile of its oral PCSK9 inhibitor in patients with high levels of “bad” cholesterol. One arm of the Phase 1 trial studied a dose of the drug, dubbed...

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Merck returns to lucrative eye disease market in up to $3B deal for EyeBio

A decade after departing the ophthalmology drug market, Merck is launching a return to the field in a $1.3 billion upfront cash acquisition for Series A-stage EyeBio. Merck could dish out another $1.7...

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Arcturus teases data from small trial of inhalable cystic fibrosis mRNA...

Arcturus Therapeutics has offered an early snapshot of its inhaled mRNA therapy’s effects in cystic fibrosis, building its case for a delivery technology designed to transport mRNA to the lung. The...

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Ikena Oncology drops cancer asset, trims headcount to save cash

Ikena Oncology has hit another speed bump as it ends work on a Phase 1 oncology candidate and plans to slash its workforce by more than half. It’s the Boston biotech’s second round of pipeline and...

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Bristol Myers pays $80M to license another Prothena neuroscience candidate

Bristol Myers Squibb is shelling out $80 million to Prothena for an exclusive global license for an early-stage neurodegenerative candidate, as the pharma giant continues to invest in its neuroscience...

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New York startup raises $33M for stem cell-derived treatment to improve IVF

Women hoping to conceive through in vitro fertilization often undergo two weeks of grueling hormone injections to mature and collect eggs. A New York startup called Gameto hopes to dramatically reduce...

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Insmed, Merus announce public offerings; AI startup raises $13M seed round

Plus, news about AEON Biopharma, Bio-Thera and STADA: Insmed to raise $500M in public offering: The startup launched the offering after it revealed positive Phase 3 data in a lung disease called...

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J&J's major depressive disorder drug hits endpoints in Phase 3 trial

Johnson & Johnson is continuing to build out its neuroscience pipeline with positive topline data for its experimental depression and insomnia drug in a late-stage trial. The drug, seltorexant, is...

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Biohaven’s autoimmune drug disappoints investors in study of healthy volunteers 

In a closely watched readout, Biohaven’s autoimmune disease treatment led to a 37% reduction on average in levels of harmful antibodies at the highest reported dose. But the reduction was not as high...

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Arrowhead touts separate Phase 2b wins for RNAi treatments in mixed...

Arrowhead Pharmaceuticals is mulling what’s next for a pair of RNA interference therapies after reporting positive data from separate mid-stage trials in mixed hyperlipidemia. As RNAi treatments, both...

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Amgen nabs FDA approval for first Soliris interchangeable biosimilar

The FDA approved Amgen’s monoclonal antibody Bkemv as the first interchangeable biosimilar for Alexion’s blockbuster Soliris to treat two types of rare blood diseases, the agency announced late...

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BioNTech to increase mRNA vaccine footprint in Africa with $145M investment

Moderna may be holding back its plans for mRNA vaccine production in Africa, but Germany’s BioNTech is filling in the space with an expanded partnership with the Coalition for Epidemic Preparedness...

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Ori Biotech, Cytiva separately unveil tech to accelerate cell therapy production

Two manufacturing tech developers have independently detailed their own approaches that could improve the cost and timelines to make cell and gene therapies and CAR-T products. On Wednesday, Ori...

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Company developing video games for ADHD announces sale

A digital therapeutics pioneer is merging with another digital health company as the field, once flush with venture cash, struggles to find its place. Akili Interactive, a public company that develops...

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Lilly's Retevmo lands new accelerated approval for pediatric cancers

The FDA on Wednesday granted another accelerated approval to Eli Lilly’s cancer drug Retevmo, this time for pediatric patients age 2 and older with certain types of thyroid cancer and solid tumors with...

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FDA approves Tris Pharma's non-stimulant pediatric ADHD liquid medication

The FDA approved Tris Pharma’s Onyda XR to treat ADHD in children who are at least 6 years old. It’s the first liquid non-stimulant ADHD drug approved in the US, the company announced Wednesday, and...

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Dollar General pulls mobile clinic mentions from website, partner no longer...

Has Dollar General quit its brief foray into healthcare services? The discount store chain, which launched a mobile healthcare clinic partnership in January 2023, appears to have removed mentions of...

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Insurance upstart Clover Health launches new business selling its tech,...

(This story is from our new Health Tech newsletter. If you’d like to sign up, just click here.) The Medicare-focused health insurer Clover Health has launched a new venture to sell its technology...

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Immunovant postpones batoclimab readouts, maps path forward for second FcRn drug

Immunovant has reshuffled plans for two of its anti-FcRn antibody drugs. The company has delayed clinical readouts by several months for its late-stage FcRn inhibitor, called batoclimab, on the heels...

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BridgeBio touts additional ATTR-CM drug data in new analyses of Phase 3 trial

BridgeBio released additional analyses of its Phase 3 study of acoramidis in ATTR-CM on Wednesday, spotlighting the link between serum transthyretin (TTR) levels and the drug’s long-term efficacy in...

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