Phase
Condition
Colon Cancer
Neoplasms
Vaginal Cancer
Treatment
xT CDx with HLA-LOH Assay
A2B694
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Key Inclusion Criteria:
Appropriately enrolled in the BASECAMP-1 A2 Biotherapeutics, Inc. study, with tissuedemonstrating LOH of HLA-A*02 by NGS (whenever possible from the primary site),successful apheresis and PBMC processing, and with sufficient stored cells availablefor Tmod CAR T-cell therapy
Histologically confirmed recurrent unresectable, locally advanced, or metastaticCRC, NSCLC, PANC, OVCA, MESO, or other solid tumors with MSLN expression. Measurabledisease is required with lesions of >1.0 cm by CT.
Received previous required therapy for the appropriate solid tumor disease asdescribed 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 safetyfollow up
Exclusion
Key Exclusion Criteria:
Has disease that is suitable for local therapy or able to receive standard of caretherapy that is therapeutic and not palliative
Prior allogeneic stem cell transplant
Prior solid organ transplant
MESO with pleural involvement extending into the peritoneum
Cancer therapy within 3 weeks or 3 half lives of A2B694 infusion
Radiotherapy within 28 days of A2B694 infusion
Unstable angina, arrhythmia, myocardial infarction, or any other significant cardiacdisease within the last 6 months
Any new symptomatic pulmonary embolism (PE) or a deep vein thrombosis (DVT) within 3months of enrollment. Therapeutic dosing of anticoagulants is allowed for history ofPE or DVT if greater than 3 months from time of enrollment, and adequately treated
History of interstitial lung disease including drug-induced interstitial lungdisease and radiation pneumonitis that requires treatment with prolonged steroids orother immune suppressive agents within 1 year
Requires supplemental home oxygen
Females of childbearing potential who are pregnant or breastfeeding
Subjects, both male and female, of childbearing potential who are not willing topractice birth control from the time of consent through 6 months post infusion ofA2B694
Study Design
Study Description
Connect with a study center
Banner Health
Gilbert, Arizona 85234
United StatesActive - Recruiting
City of Hope
Duarte, California 91010
United StatesSite Not Available
UCSD Moores Cancer Center
La Jolla, California 92093
United StatesActive - Recruiting
UCLA Medical Center
Los Angeles, California 90404
United StatesActive - Recruiting
Stanford University
Stanford, California 94305
United StatesActive - Recruiting
Mayo Clinic
Jacksonville, Florida 32224
United StatesActive - Recruiting
Moffitt Cancer Center
Tampa, Florida 33606
United StatesActive - Recruiting
Massachusetts General Hopsital/Dana Farber Cancer Center
Boston, Massachusetts 02114
United StatesActive - Recruiting
Mayo Clinic Rochester
Rochester, Minnesota 55905
United StatesActive - Recruiting
Washington University
Saint Louis, Missouri 63110
United StatesSite Not Available
Washington University
St. Louis, Missouri 63110
United StatesActive - Recruiting
NYU Langone Medical Center
New York, New York 10016
United StatesActive - Recruiting
MD Anderson Cancer Center
Houston, Texas 77030
United StatesSite Not Available
Fred Hutchinson Cancer Center
Seattle, Washington 98109
United StatesActive - Recruiting
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