Sarepta Therapeutics faces an "arduous path” to try to get its gene therapy for Duchenne muscular dystrophy back onto the market, a senior FDA official told STAT.

One of the few drug trials for a possible long Covid ended in disappointment. But lessons are leading to a second chance.

This is the web edition of D.C. Diagnosis, STAT's twice-weekly newsletter about the politics and policy of health and ...

More than one-third of people who helped develop the 2023 guidelines for treating children with obesity had undisclosed ...

In today's Morning Rounds newsletter: a failed long Covid drug may get another shot, the benefits of even a little activity ...

Sarepta Therapeutics reversed course and agreed to halt all shipments of Elevidys, its gene therapy for Duchenne muscular ...

Join Bill Gates and a range of experts for a discussion on flattening barriers to improving women’s health — from research ...

New AI chatbot called Ash is different, Slingshot founders say, because its training model is based on real therapeutic ...

The FDA on Tuesday rejected a skin therapy from Replimune Group, suggesting a hardened stance on drug approvals under new agency officials ...

Sarepta will halt all shipments of Elevidys, its drug for Duchenne muscular dystrophy patients, by Tuesday evening.

Worsening a patient's credit can prevent them from getting a job, renting an apartment, or even paying their outstanding ...

A race to develop a new class of drugs could transform treatment for patients with narcolepsy — as well as for patients with ...