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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
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

Full criteria on ClinicalTrials.gov

Sites (11)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Princess Margaret Cancer Centre
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TorontoCanadaUnknown status
Roswell Park Cancer Institute
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BuffaloUnited StatesUnknown status
Ohio State University Wexner Medical Center
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ColumbusUnited StatesUnknown status
Duke University Medical Center, Duke Cancer Institute
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DurhamUnited StatesUnknown status
M D Anderson Cancer Center
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HoustonUnited StatesUnknown status
University of Miami
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MiamiUnited StatesUnknown status
Tennessee Oncology - Sarah Cannon Research Institute
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NashvilleUnited StatesUnknown status
Fox Chase Cancer Center
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PhiladelphiaUnited StatesUnknown status
Washington University School of Medicine
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St LouisUnited StatesUnknown status
Washington University
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St LouisUnited StatesUnknown status
Moffitt Cancer Center
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TampaUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.