The targeted therapy sunvozertinib was more effective than standard platinum-based chemotherapy as a first-line treatment for patients with advanced non-small cell lung cancer (NSCLC) driven by EGFR ...

Researchers say a single intravenous ketamine infusion can rapidly relieve severe depression and suicidal thoughts when traditional antidepressants fail.

Sanofi has received a priority review from the US Food and Drug Administration (FDA) for its new drug application (NDA) for venglustat, an oral glucosylceramide synthase inhibitor (GCSi) intended for ...

Replimune (REPL) stock surged after the company announced plans to resubmit a marketing application for its lead asset, RP1, in the U.S. Read more here.

A chocolate snack marketed as almond- and coconut-based is being pulled because of what may be hiding inside.Bazzini, LLC, of ...

Experimental melanoma drug was rejected twice because the Food and Drug Administration questioned its study design.

Replimune was among the drugmakers that had criticized the FDA for what they called inconsistent guidance around trials and approvals.

To stay on forefront of research, UL should move away from animal testing, argues guest columnist Jennifer Riedl Cross ...

According to the department, the Hepcludex injection is the first treatment for hepatitis delta virus (HDV) in adults lacking cirrhosis or with compensated cirrhosis. “Today’s approval fills a ...

Within 24 hours of injecting the first dose of a weight loss medication she received following a visit with a telehealth ...

A freezer-case favorite is being pulled from stores over allergy concerns.De Dios’s Ice Pops II LLC, of Paterson, New Jersey, ...

The FDA approved the antibody-drug conjugate pivekimab sunirine (Decnupaz) for the rare hematologic malignancy blastic ...