ABI-201 is undergoing IND-enabling studies and uses the same capsid as the firm's clinical-stage gene therapy candidate for wet AMD.

In a recent trial, researchers found that Xpovio plus chemo had activity in NSCLC patients with KRAS mutations other than ...

Based on early Phase I/II data, investigators at Cincinnati Children's are enrolling more patients with a telomere biology ...

The first patient, who had xerostomia linked with Sjögren's disease, received the autologous cell therapy as part of a Phase ...

The firm said it will rely on academic partnerships and contract manufacturers to support its cell therapy clinical trials.

Approval would expand the use of Enhertu to breast cancer patients with nearly undetectable HER2 levels in their tumors.

SciClone will develop and distribute Tasfygo in greater China but Eisai will retain worldwide rights outside the region.

The committee supports approving the CFTR modulator for patients 2 years and older with at least one non-class I CFTR gene mutation.

The European Commission had requested the committee consider new data on the drug that became available after it had adopted its positive opinion.

Krystal said it is on track to launch Vyjuvek in Germany in the middle of the year and in France later in 2025.