Neurologists from multiple clinics presented data at AAIC on Leqembi's use, shedding light on its safety and efficacy outside ...

The FDA investigated the death of a boy in Brazil on Elevidys and concluded it was unrelated to the treatment.

The FDA investigated the death of a boy in Brazil on Elevidys and concluded it was unrelated to the treatment.

NEW YORK – The European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) has recommended regulators approve Servier's IDH1/2 inhibitor Voranigo (vorasidenib) as a treatment for ...

Trontinemab is a formulation of Roche's failed gantenerumab but now paired with the company's Brainshuttle technology to ...

The therapies, which are just starting to enter clinical trials, will need to prove clear clinical and quality-of-life ...

The Medicines and Healthcare Products Regulatory Agency said it will closely track adverse events associated with the treatment.

Blood Cancer UK is launching early career grants following a tough pandemic-era funding climate, while US funders worry about ...

Despite regulatory setbacks, the petitioners believe that survival and other data they've collected themselves are worth ...

The trial will test several treatment approaches in the maintenance setting for extensive stage small cell lung cancer.

In a new paper, a team from Yale and Fred Hutch has found autoantibody reactivity could predict cancer patients' response to ...

Sarepta maintains it reported the incident to the FDA in June, and the boy's doctor had deemed his death was unrelated to treatment.