TC BioPharm (NASDAQ: TCBP) announced encouraging progress in its ACHIEVE Phase 2b trial in the UK, with three patients completing the full-dose regimen of TCB008 with no drug-related adverse events. The trial, evaluating TCB008 for AML and MDS/AML, has enrolled 10 patients so far, with nine receiving their second dose, four their third dose, and three their final dose. Preliminary safety data indicates the 5mL dose is well-tolerated, supporting the study’s safety objectives. Recruitment has advanced swiftly, with nine of 14 planned patients for Cohort A (relapsed/refractory disease) and one for Cohort B (minimal residual disease) enrolled. Company executives noted the trial’s rapid progress and the potential for expedited review in Cohort B, as the team focuses on completing recruitment and data analysis in 2025.
To view the full press release, visit: https://ibn.fm/82A88
About TC BioPharm Holdings PLC
TC BioPharm is a clinical stage biopharmaceutical company focused on the discovery, development and commercialization of gamma-delta T cell therapies for the treatment of cancer with human efficacy data in acute myeloid leukemia. Gamma-delta T cells are naturally occurring immune cells that embody properties of both the innate and adaptive immune systems and can intrinsically differentiate between healthy and diseased tissue. TC BioPharm is the leader in developing gamma-delta T cell therapies, and the first company to conduct phase II/pivotal clinical studies in oncology. The company is conducting two investigator-initiated clinical trials for its unmodified gamma-delta T cell product line – Phase 2b/3 pivotal trial for OmnImmune(R) in treatment of acute myeloid leukemia using the company’s proprietary allogeneic CryoTC technology to provide frozen product to clinics worldwide. For more information about the company, visit www.tcbioparm.com.
NOTE TO INVESTORS: The latest news and updates relating to TCBP are available in the company’s newsroom at https://ibn.fm/TCBP
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