Imugene Limited Advances Azer-Cel to Potential Pivotal Trial with FDA Fast Track Designation for DLBCL
Imugene Limited, an immuno-oncology company, has announced significant progress in its Phase 1b clinical trial for azer-cel (azercabtagene zapreleucel), targeting relapsed/refractory diffuse large B-cell lymphoma (DLBCL). The U.S. FDA has granted Fast Track Designation for azer-cel, aimed at expediting the development and review process for treatments addressing serious conditions with unmet medical needs. This designation provides Imugene with benefits such as more frequent FDA meetings, rolling review of submissions, and potential eligibility for Accelerated Approval and Priority Review. Imugene plans to meet with the FDA in Q4 2025 to discuss a pivotal study for azer-cel, following promising trial results indicating significant patient responses.
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. Imugene Limited published the original content used to generate this news brief via PR Newswire (Ref. ID: CN29255) on July 14, 2025, and is solely responsible for the information contained therein.
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