NCT03132922Active, not recruitingPhase 1
MAGE-A4ᶜ¹º³²T for Multi-Tumor
Phase 1 Dose Escalation, Multi-tumor Study to Assess the Safety, Tolerability and Antitumor Activity of Genetically Engineered MAGE-A4ᶜ¹º³²T in HLA-A2+ Subjects With MAGE-A4 Positive Tumors
Source: ClinicalTrials.gov · Last updated 4 Jun 2026
Brief summary (registry, in English)
This study will investigate the safety and tolerability of MAGE-A4ᶜ¹º³²T cell therapy in subjects who have the appropriate HLA-A2 tissue marker and whose urinary bladder, melanoma, head and neck, ovarian, non-small cell lung, esophageal, gastric, synovial sarcoma, or myxoid/round call liposarcoma (MRCLS) tumor has the MAGE-A4 protein expressed. This study will take a subject's T cells and give them a T cell receptor protein that recognizes and attacks the tumors. This study has a substudy component that will investigate the safety and tolerability of MAGE-A4c1032T cell therapy in combination with low dose radiation in up to 10 subjects.
- Status (registry)
- Active, not recruiting
- Phase (registry)
- Phase 1
- Study type
- Interventional
- Enrollment
- 71 (actual)
- First submitted
- 25 Apr 2017
- Start date
- 15 May 2017
- Primary completion date
- 27 Dec 2022
- Lead sponsor
- USWM CT, LLC
- Diseases
- Head and neck cancer, Bladder cancer, Melanoma, Lung cancer, Gastric and esophageal cancer, Ovarian cancer, Sarcoma
- NCT number
- NCT03132922
What you commit to
- Study type: Interventional · Phase 1
- Participants enrolled: 71
- From 15 May 2017 to the primary completion date, 27 Dec 2022
- 11 sites in 2 countries
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Subject is receiving excluded therapy/treatment per protocol
- Subject has any other active malignancy besides the tumor under study within 3 years prior to Screening. Subject has uncontrolled intercurrent illness.
- Subject is pregnant or breastfeeding.
- Additional Exclusion Criteria for the Radiation Substudy:
- Subject does not have at least one target lesion amenable to radiation.
- Certain radiation therapy within 6 months of clinical trial are an exclusion.
Other illness
- Subject has active infection with HIV, HBV, HCV or HTLV
- Metastatic disease impinging on the spinal cord or threatening spinal cord compression.
Other
- Subject does not express appropriate HLA-A genotype
- Subject has symptomatic CNS metastases.
- Subject does not meet eligibility criteria for the main study (ADP-0044-001).
Who the study is looking for
- Subject is ≥18 to 75 years of age at the time of signing the study informed consent.
- Subject has histologically confirmed diagnosis of any one of the indicated tumor types
- Subject is HLA-A\*02 positive. (This determination will be made under screening protocol ADP-0000-001).
- Subject's tumor shows expression of the MAGE-A4 RNA or protein. (This determination will be made under screening protocol ADP-0000-001).
- Adequate organ function as indicated in the study protocol
- Subject has measurable disease according to RECIST v1.1 criteria prior to lymphodepletion
- Subject meets disease-specific requirements per protocol
- 7\. Subject has anticipated life expectancy \> 6 months prior to leukapheresis and \>3 months prior to lymphodepletion.
Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers
Sites (11)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Princess Margaret Cancer Centre Coordinator of this site? Confirm its status | Toronto | Canada | Unknown status |
| Roswell Park Cancer Institute Coordinator of this site? Confirm its status | Buffalo | United States | Unknown status |
| Ohio State University Wexner Medical Center Coordinator of this site? Confirm its status | Columbus | United States | Unknown status |
| Duke University Medical Center, Duke Cancer Institute Coordinator of this site? Confirm its status | Durham | United States | Unknown status |
| M D Anderson Cancer Center Coordinator of this site? Confirm its status | Houston | United States | Unknown status |
| University of Miami Coordinator of this site? Confirm its status | Miami | United States | Unknown status |
| Tennessee Oncology - Sarah Cannon Research Institute Coordinator of this site? Confirm its status | Nashville | United States | Unknown status |
| Fox Chase Cancer Center Coordinator of this site? Confirm its status | Philadelphia | United States | Unknown status |
| Washington University School of Medicine Coordinator of this site? Confirm its status | St Louis | United States | Unknown status |
| Washington University Coordinator of this site? Confirm its status | St Louis | United States | Unknown status |
| Moffitt Cancer Center Coordinator of this site? Confirm its status | Tampa | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.