The study introduces a Conditional Generative AI Model designed to create synthetic full-body CT scans based on patient ...
The FDA accepted a supplemental biologics license application for Opdivo plus Yervoy as a first-line treatment for some adult ...
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GlobalData on MSNMeiraGTx seeks UK approval after gene therapy restores sight in children born blindMeiraGTx’s investigational gene therapy AAV-AIPL1 has improved the sight of 11 children who were born blind. MeiraGTx is ...
Undiagnosed mental health sufferers hurt their loved ones along with others by lacking proper treatment particularly when ...
The US FDA has approved Merilog (insulin-aspart-szjj) as a biosimilar to Novolog (insulin aspart) for adults and pediatric patients with diabetes.
NexoBrid ® is a topically administered biological orphan drug that enzymatically removes eschar while preserving viable ...
Ladies and gentlemen, good morning and welcome to the Taysha Gene Therapies Full Year 2024 Conference Call. At this time all participants are in listen-only mode. A brief question-and-answer session ...
Insulin-aspart-szjj is the first rapid-acting insulin biosimilar approved and the third insulin product approved by the FDA.
The FDA has authorized Humacyte to release commercial shipments –– Positive responses from surgeons and trauma centers to initial sales and ...
Hundreds of children in England with a rare and severe form of epilepsy are set to benefit from a new drug being rolled out ...
The medical expert noted that the frequency of these checkups largely depends on factors such as age, overall health, and ...
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