Citius Oncology Inc. reported preliminary topline safety and efficacy data from an investigator-initiated Phase 1 trial evaluating LYMPHIR (E7777, denileukin diftitox-cxdl) administered prior to commercial CD19-directed CAR-T therapy in 14 patients with high-risk relapsed or refractory diffuse large B-cell lymphoma. The company said the overall response rate at one month was 86%, including 57% complete responses and 29% partial responses, with no dose-limiting toxicities observed up to 9 µg/kg. The results were presented at the 2026 ASTCT and CIBMTR Tandem Meetings.
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. Citius Oncology Inc. published the original content used to generate this news brief via PR Newswire (Ref. ID: NY99538) on March 04, 2026, and is solely responsible for the information contained therein.
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