Gilead Sciences' Kite Division Receives FDA Approval for Expanded Use of Yescarta in Lymphoma Treatment.

sábado, 7 de febrero de 2026, 11:13 am ET1 min de lectura
GILD--

Gilead Sciences' Kite division received FDA approval for a label update on its CAR-T therapy, Yescarta, removing a restriction for relapsed or refractory primary central nervous system lymphoma. Despite recent regulatory success, Gilead faces challenges with slowing revenue growth and insider selling activity. The company operates in the healthcare sector and has a market capitalization of $186.12 billion.

Gilead Sciences' Kite Division Receives FDA Approval for Expanded Use of Yescarta in Lymphoma Treatment.

Comentarios



Add a public comment...
Sin comentarios

Aún no hay comentarios