Phase 1 Study to Investigate TCRTs KRAS Mutation in Unresectable, Advanced, and/or Metastatic Solid Tumors
Trial Status: active
Phase I Study, a master protocol to investigate TCR-Engineered T cells recognizing KRAS mutations in adult subjects with Unresectable, Advanced, and/or Metastatic Solid Tumors.
Inclusion Criteria
- Age ≥18 years
- Diagnosed with NSCLC, Colorectal adenocarcinoma, Pancreatic adenocarcinoma, Endometrial Cancer or any other solid tumor
- Tumors must harbor a KRAS G12D variant mutation and subject must be HLA-C*08:02 positive, HLA-A*11:01 or HLA-A*11:02 positive in at least one allele
- Subject has advanced solid cancer, defined as unresectable, advanced, and/or metastatic disease (Stage III or IV) after at least 1 line of approved systemic standard of care (SOC) treatment regimen and for which there are no available curative treatment options.
- Presence of at least 1 measurable lesion per RECIST v1.1
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1 at the time of enrollment Key
Exclusion Criteria
- Any other primary malignancy within the 3 years prior to enrollment (except for non-melanoma skin cancer, carcinoma in situ (eg, cervix, bladder, breast) or low-grade prostate cancer
- Known, active primary central nervous system (CNS) malignancy
- History of prior adoptive cell and gene therapy, allogeneic stem cell transplant or solid organ transplantation.
- History of stroke or transient ischemic attack within the 12 months prior to enrollment.
- History of clinically significant cardiac disease within the 6 months prior to enrollment or heart failure at any time prior to enrollment.
- Systemic therapy within at least 2 weeks or 3 half-lives, whichever is shorter, prior to enrollment.
- Any form of primary immunodeficiency.
- Active immune-mediated disease requiring systemic steroids or other immunosuppressive treatment (except if related to prior checkpoint inhibitor therapy)
- Female of childbearing potential who is lactating or breast feeding at the time of enrollment
- Prior treatment with pan-KRAS or KRAS G12D targeting agents unless presence of KRAS G12D mutation is confirmed after the completion of treatment with pan-KRAS or KRAS G12D targeting agents.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT06218914.
Locations matching your search criteria
United States
California
Los Angeles
UCLA / Jonsson Comprehensive Cancer Center
Status: Active
Contact: Christopher Hannigan
Phone: 310-794-6500
Email: CHannigan@mednet.ucla.edu
Florida
Jacksonville
Mayo Clinic in Florida
Status: Active
Name Not AvailableIllinois
Chicago
University of Chicago Comprehensive Cancer Center
Status: Active
Name Not AvailableKansas
Kansas City
University of Kansas Cancer Center
Status: Active
Name Not AvailableMassachusetts
Boston
Brigham and Women's Hospital
Status: Active
Name Not AvailableDana-Farber Cancer Institute
Status: Active
Name Not AvailableMissouri
Saint Louis
Siteman Cancer Center at Washington University
Status: Active
Name Not AvailableNew York
New York
Laura and Isaac Perlmutter Cancer Center at NYU Langone
Status: Active
Name Not AvailableMemorial Sloan Kettering Cancer Center
Status: Active
Name Not AvailablePennsylvania
Philadelphia
Thomas Jefferson University Hospital
Status: Active
Name Not AvailablePittsburgh
UPMC Hillman Cancer Center
Status: Active
Name Not AvailableTexas
Dallas
UT Southwestern/Simmons Cancer Center-Dallas
Status: Active
Name Not AvailableThis is a Phase 1, open-label, Phase 1, Multi-Center Master Protocol to evaluate the
safety and preliminary Anti-Tumor activity of TCR-Engineered T cells (KRAS TCRTs)
recognizing KRAS mutations in adult subjects with Unresectable, Advanced, and/or
Metastatic Solid Tumors.
Trial PhasePhase I
Trial Typetreatment
Lead OrganizationAstraZeneca Pharmaceuticals LP
- Primary IDNT-112-301
- Secondary IDsNCI-2024-01226
- ClinicalTrials.gov IDNCT06218914