Kite Pharma, a Gilead Science Inc company GILD, churned out more data for its CAR-T Yescarta in first-line lymphoma patients.
- The Company shared the data at the American Society of Hematology (ASH) Annual Meeting & Exposition.
- In updated results from the Phase 2 ZUMA-12 study, Yescarta posted a 78% complete response rate among 37 patients with high-risk large B cell lymphoma at a median follow-up of 15.9 months.
- All median survival checkpoints hadn't been reached at a median of 15.9 months after infusion. Still, Kite floated 12-month outcomes estimates of 81% for durable responders, 73% for event-free survival, 75% for progression-free survival, and 91% for patients alive.
- On the safety front, grade 3 or higher cytokine release syndrome occurred in 8% of patients, and 23% experienced a Grade 3 or higher neurological event.
- There were no deaths tied to treatment with Yescarta, although one patient died from COVID-19.
- All but one CRS and neurological events were resolved through treatment by the data cutoff.
- Related Link: Gilead's Kite Unveils More Data On Yescarta In Second-Line Lymphoma Patients.
- Price Action: GILD shares closed at $70.61 on Monday.
- Check out our coverage of the American Society of Hematology (ASH) Annual Meeting 2021 here.
© 2024 Benzinga.com. Benzinga does not provide investment advice. All rights reserved.
Comments
Loading...
Benzinga simplifies the market for smarter investing
Trade confidently with insights and alerts from analyst ratings, free reports and breaking news that affects the stocks you care about.
Join Now: Free!
Already a member?Sign in