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Creative Medical Technology Holdings Secures FDA Clearance for Expanded Dose Escalation in the Clinical Trial of CELZ-201-DDT for Chronic Lower Back Pain

Positive Interim Blinded Data Supports Advancement Toward Potential Pivotal Phase 3 StudyPHOENIX, March 20, 2025 (GLOBE NEWSWIRE) -- Creative Medical Technology Holdings, Inc. (NASDAQ: CELZ) (the “Company”), a clinical-stage biotechnology company specializing in regenerative medicine, today announced that the U.S. Food and Drug Administration (FDA) has cleared an expanded dose escalation for its ongoing Phase 1/2 trial of StemSpine® using AlloStem™ (CELZ-201-DDT), the Company’s proprietary allog

articleCreative Medical Technology Holdings, Inc.March 20, 20253/company/creative-medical-technology-holdings-inc/news/creative-medical-technology-holdings-secures-115000650
Creative Medical Technology Holdings Secures FDA Clearance for Expanded Dose Escalation in the Clinical Trial of CELZ-201-DDT for Chronic Lower Back Pain

About this update from Creative Medical Technology Holdings, Inc.

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More updates from Creative Medical Technology Holdings, Inc.

regenerative medicineData Safety Monitoring BoardFood and Drug Administrationchronic back painMedical TechnologyInstitutional Review Boardcell therapytrial participants