Estrella Immunopharma Inc. announced that its STARLIGHT-1 clinical trial has advanced to Phase II following a positive recommendation from an independent Data Safety Monitoring Board (DSMB). The decision was based on safety data from the Phase I dose escalation phase, during which no treatment-related serious adverse events were reported among nine patients, and all evaluable patients in the high-dose cohort achieved a complete response at Month 1. The STARLIGHT-1 trial is evaluating EB103, a CD19-redirected ARTEMIS® T-cell therapy, in patients with relapsed or refractory B-cell non-Hodgkin's lymphoma. The expansion phase will further assess safety and preliminary efficacy, with results to be collected and used to inform future pivotal trial strategies. Results from the expansion phase have not yet been presented.
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. Estrella Immunopharma Inc. published the original content used to generate this news brief via Business Wire (Ref. ID: 20251204012425) on December 04, 2025, and is solely responsible for the information contained therein.
Comments