Allogene Therapeutics Inc. has reported a favorable outcome in arbitration related to its collaboration with Servier and Cellectis. The tribunal rejected Cellectis's claims regarding alleged breaches by Servier and denied financial claims for milestone payments, stating that such payments are not due until FDA acceptance of a Biologics License Application. The ruling also ordered only a partial termination of the license, limited to the UCART19 V1 product, which was discontinued in 2021. Allogene retains full control of cemacabtagene ansegedleucel (cema-cel), with its expanded sub-license covering the EU and UK and options for Japan and China, facilitating Allogene's path to potentially acquire full global rights to cema-cel.
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. Allogene Therapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9602670-en) on December 15, 2025, and is solely responsible for the information contained therein.
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