Creative Medical Technology Holdings Completes Enrollment in FDA-Cleared CELZ-201 Trial
Creative Medical Technology Holdings Inc. has announced the successful completion of patient enrollment in its FDA-cleared ADAPT clinical trial for CELZ-201 (Olastrocel), a proprietary perinatal tissue-derived cell therapy targeting chronic lower back pain associated with degenerative disc disease. The company reported that a positive safety review by an independent Data Safety Monitoring Board found no significant adverse events, supporting the continued advancement of the trial. Topline safety and efficacy results have not yet been presented and are expected in the future as the company advances toward later-stage development and potential commercialization.
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. Creative Medical Technology Holdings Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 9603294) on December 17, 2025, and is solely responsible for the information contained therein.
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