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

Status: Recruiting
Location: See all (11) locations...
Intervention Type: Diagnostic test, Biological
Study Type: Interventional
Study Phase: Phase 1/Phase 2
SUMMARY

The goal of this study is to test A2B694, an autologous logic-gated Tmod™ CAR T-cell product in subjects with solid tumors including colorectal cancer (CRC), pancreatic cancer (PANC), non-small cell lung cancer (NSCLC), ovarian cancer (OVCA), mesothelioma (MESO), and other solid tumors that express MSLN and have lost HLA-A\*02 expression. The main questions this study aims to answer are: Phase 1: What is the recommended dose of A2B694 that is safe for patients Phase 2: Does the recommended dose of A2B694 kill the solid tumor cells and protect the patient's healthy cells Participants will be required to perform study procedures and assessments, and will also receive the following study treatments: Enrollment and Apheresis in BASECAMP-1 (NCT04981119) Preconditioning Lymphodepletion (PCLD) Regimen A2B694 Tmod CAR T cells at the assigned dose

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Appropriately enrolled in the BASECAMP-1 A2 Biotherapeutics, Inc. study, with tissue demonstrating LOH of HLA-A\*02 by NGS (whenever possible from the primary site), successful apheresis and PBMC processing, and with sufficient stored cells available for Tmod CAR T-cell therapy

• Histologically confirmed recurrent unresectable, locally advanced, or metastatic CRC, NSCLC, PANC, OVCA, MESO, or other solid tumors with MSLN expression. Measurable disease is required with lesions of \>1.0 cm by CT.

• Received previous required therapy for the appropriate solid tumor disease as described in the protocol

• Has adequate organ function as described in the protocol

• ECOG performance status of 0 to 1

• Life expectancy of ≥3 months

• Willing to comply with study schedule of assessments including long term safety follow up

Locations
United States
Arizona
Banner Health
RECRUITING
Gilbert
California
UCSD Moores Cancer Center
RECRUITING
La Jolla
UCLA Medical Center
RECRUITING
Los Angeles
Stanford University
RECRUITING
Stanford
Florida
Mayo Clinic
RECRUITING
Jacksonville
Moffitt Cancer Center
RECRUITING
Tampa
Massachusetts
Massachusetts General Hopsital/Dana Farber Cancer Center
RECRUITING
Boston
Minnesota
Mayo Clinic Rochester
RECRUITING
Rochester
Missouri
Washington University
RECRUITING
St Louis
New York
NYU Langone Medical Center
RECRUITING
New York
Washington
Fred Hutchinson Cancer Center
RECRUITING
Seattle
Contact Information
Primary
Clinical Trials
ClinicalTrials@a2bio.com
310-431-9180
Time Frame
Start Date: 2024-04-03
Estimated Completion Date: 2029-06
Participants
Target number of participants: 230
Treatments
Experimental: A2B694
Patients receive Preconditioning Lymphodepletion (PCLD) Regimen followed by a single dose of A2B694 intravenously on day 0
Sponsors
Leads: A2 Biotherapeutics Inc.
Collaborators: Tempus AI

This content was sourced from clinicaltrials.gov

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