
Missouri Surgeons Separate Twins Conjoined at Head
Surgeons at a Missouri children's hospital successfully separated infant twin sisters born conjoined at the head earlier this year, according to a hospital

Surgeons at a Missouri children's hospital successfully separated infant twin sisters born conjoined at the head earlier this year, according to a hospital

Novo Nordisk has entered a collaboration with AI company Anthropic to speed up drug discovery and development, with an initial project testing the Claude

The FDA has opened a pilot program pairing drug sponsors with qualified research institutions to expedite IND reviews, aiming to cut phase 1 trial

The phase III EVOKE-03 trial found adding the antibody-drug conjugate sacituzumab govitecan to pembrolizumab immunotherapy did not significantly improve

In a phase 3 trial, adding zipalertinib to chemotherapy improved median progression-free survival to 14.5 months, a six-month gain over chemo alone, for
GSK and Hansoh Pharma's antibody-drug conjugate risvutatug rezetecan achieved a median overall survival of 18.5 months in a phase 3 trial for relapsed

The FDA has postponed its approval decision for Exelixis' oral kinase inhibitor zanzalintinib in metastatic colorectal cancer, requesting updated data and

The biologic drug tozorakimab, which targets interleukin-33, significantly reduced the rate of moderate and severe exacerbations in patients with COPD

Kura Oncology has spun out a new biotech startup, Caspian Therapeutics, to develop menin inhibitor drugs for diabetes and cardiometabolic diseases.

Kura Oncology has created spinout Caspian Therapeutics, backed by $50 million from investors including Eli Lilly, to advance menin inhibitor KO-7246 for

A large real-world study presented at the ERS Congress found patients with asthma or COPD who started a GLP-1 drug had a 14% lower risk of severe

The FDA granted accelerated approval to AstraZeneca's camizestrant (Etcamah) for HR-positive, HER2-negative breast cancer patients with an ESR1 mutation

Roivant's mosliciguat reduced a key lung pressure measure by 56% in a Phase 2 trial for PH-ILD, with analysts citing multi-billion dollar potential.

Moonwalk Biosciences has raised $70 million in Series B funding to advance a pipeline of RNA interference drugs for obesity, pivoting from its original

A small trial found adjunctive ketamine was more effective than midazolam for treatment-resistant bipolar depression.


ADARx Pharmaceuticals has filed for an initial public offering to raise funds for advancing its pipeline of siRNA therapies, including mid- and late-stage

Novartis's pelacarsen, an antisense drug developed with Ionis to lower lipoprotein(a), did not reduce major cardiovascular events in high-risk patients in

A randomized trial found the AI system Prof. Valmed cut diagnosis time by more than half compared to physicians working alone, but did not improve

Novo Nordisk has discontinued two late-stage heart failure trials for its drug ziltivekimab after a data review, leaving one remaining study to determine

Akeso and Summit Therapeutics report their bispecific antibody ivonescimab helped lung cancer patients live longer than those on Merck's Keytruda in a

The first FDA-approved PROTAC drug for breast cancer has validated a new class of medicines that work by bringing proteins together.

A secret shopper study in JAMA Health Forum reveals compounded GLP-1 drugs for weight loss remain widely available in West Virginia and Oklahoma despite

Infectious disease biotech Invivyd has appointed board chairman Marc Elia as its new CEO, with the leadership change coming ahead of key phase 3 trial

Novartis and Ionis Pharmaceuticals' experimental drug pelacarsen failed to reduce heart attacks, strokes or death in a Phase 3 study of over 8,000 people.

The FDA has approved Ionis Pharmaceuticals' Zanvastro, the first treatment for the rare neurological disorder Alexander disease.

A new Lancet Series argues that cardiovascular care in pregnancy must shift from reacting to crises to anticipating and managing long-term risk, stating up

The FDA has granted accelerated approval to AstraZeneca's Etcamah for HR-positive, HER2-negative advanced breast cancer with ESR1 mutations, based on a
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