A Seamless Phase 1/2 Study to Evaluate the Safety and Efficacy of A2B694, an Autologous Logic-gated Tmod™ CAR T, in Heterozygous HLA-A*02 Adults with Recurrent Unresectable, Locally Advanced, or Metastatic Solid Tumors That Express MSLN and Have Lost HLA-A*02 Expression
Latest Information Update: 28 May 2026
At a glance
- Drugs A2B 543 (Primary) ; A2B-694 (Primary)
- Indications Colorectal cancer; Gastric cancer; Mesothelioma; Neuroendocrine carcinoma; Non-small cell lung cancer; Oesophageal cancer; Ovarian cancer; Pancreatic cancer; Solid tumours
- Focus Adverse reactions; First in man; Therapeutic Use
- Acronyms EVEREST-2
- Sponsors A2 Biotherapeutics
Most Recent Events
- 21 Apr 2026 According to A2 Bio media release, data from this trial will be presented at the during the 2026 Annual Meeting of the American Society of Clinical Oncology taking place May 29-June 2, 2026, in Chicago.
- 26 Feb 2026 According to A2 Bio media release, the first patient dosed with A2B543, initiating the second arm of the Phase 1/2 EVEREST-2 study.
- 08 Jan 2026 According to A2 Bio media release, the U.S. Food and Drug Administration (FDA) has cleared the IND for A2B543 for the treatment of germline heterozygous HLA-A*02 adults with recurrent unresectable, locally advanced, or metastatic solid tumors. It will be evaluated as a second arm of the EVEREST-2 master protocol (NCT06051695) in patients with colorectal cancer, pancreatic cancer, non-small cell lung cancer, ovarian cancer, mesothelioma, and other solid tumors that express mesothelin (MSLN).