AbbVie says EU clears Tepkinly combo for relapsed or refractory follicular lymphoma
AbbVie, Inc.
AbbVie, Inc. ABBV | 0.00 |
- European Commission granted AbbVie marketing authorization for Tepkinly (epcoritamab) with lenalidomide, rituximab in relapsed or refractory follicular lymphoma.
- Authorization covers second-line use, positioning the regimen as a chemotherapy-free bispecific-based option in Europe.
- Phase 3 EPCORE FL-1 showed 79% lower risk of progression or death vs R2 alone (HR 0.21; p<0.0001).
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. AbbVie Inc. published the original content used to generate this news brief via PR Newswire (Ref. ID: EN86738) on July 06, 2026, and is solely responsible for the information contained therein.
