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NCT06964737 · ClinicalTrials.gov registry record · Phase 1

Anti-GARP Chimeric Antigen Receptor T Cell Therapy for the Treatment of Recurrent Grade III or IV Gliomas

A Phase 1 study of Recurrent Malignant Glioma and WHO Grade 3 Glioma, sponsored by Ohio State University Comprehensive Cancer Center.

Recruiting
Registry status
Phase 1
Development phase
30
Enrollment target
1
Study location

NCT06964737: Recruiting Phase 1 study of Recurrent Malignant Glioma and WHO Grade 3 Glioma, sponsored by Ohio State University Comprehensive Cancer Center.

NCT06964737 is a Phase 1 study of Recurrent Malignant Glioma and WHO Grade 3 Glioma that is actively recruiting participants, run by Ohio State University Comprehensive Cancer Center. The registered enrollment target is 30 participants, above the 25-participant average among 17 other Recurrent Malignant Glioma trials with a reported enrollment target (20% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06964737, a Phase 1 study of Recurrent Malignant Glioma and WHO Grade 3 Glioma, is actively recruiting participants, sponsored by Ohio State University Comprehensive Cancer Center.

RECRUITING
Registry status
Phase 1
Development phase
30 participants
Enrollment target
1
Study location

Study Summary

This phase I trial tests the safety, side effects, and best dose of anti-glycoprotein-A repetitions predominant (GARP) chimeric antigen receptor (CAR) T cell therapy and how well it works in treating patients with grade III or IV gliomas that have come back after a period of improvement (recurrent). CAR T-cell therapy is a type of treatment in which a patient's T cells (a type of immune system cell) are changed in the laboratory so they will attack tumor cells. T cells are taken from a patient's blood. Then the gene for a special receptor that binds to a certain protein, such as GARP, on the patient's tumor cells is added to the T cells in the laboratory. The special receptor is called a CAR. Large numbers of the CAR T cells are grown in the laboratory and given to the patient by infusion for treatment of certain tumors. Giving anti-GARP CAR T cell therapy may be safe, tolerable, and/or effective in treating patients with recurrent grade III or IV gliomas.

Primary Outcome

The rate, frequency and severity will be defined using Common Terminology Criteria for Adverse Events (CTCAE) version (v) 5. Will be summarized by descriptive statistics. The maximum grade for each type of toxicity will be recorded for each patient, and frequency tables will be reviewed to determine toxicity patterns.

Interventions

  • PROCEDURE Biospecimen Collection
  • PROCEDURE Magnetic Resonance Imaging
  • PROCEDURE Echocardiography Test
  • PROCEDURE Chest Radiography
  • BIOLOGICAL Anti-GARP Chimeric Antigen Receptor-T Cells

Study Locations (1)

Ohio

  • Ohio State University Comprehensive Cancer Center - Columbus

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2025-05-21
Est. Completion 2026-12-31
Phase Phase 1

What NCT06964737 shows while recruiting

NCT06964737 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, above the 25-participant average among 17 other Recurrent Malignant Glioma trials with a reported enrollment target (20% higher).

The record links to 6 conditions, with Recurrent Malignant Glioma appearing as the primary indexed condition, and to 5 interventions - of which Biospecimen Collection is the first listed.

NCT06964737 reports a single indexed study location in Ohio.

Frequently Asked Questions

What is clinical trial NCT06964737 about?

NCT06964737 is a clinical study titled "Anti-GARP Chimeric Antigen Receptor T Cell Therapy for the Treatment of Recurrent Grade III or IV Gliomas". This phase I trial tests the safety, side effects, and best dose of anti-glycoprotein-A repetitions predominant (GARP) chimeric antigen receptor (CAR) T cell therapy and how well it works in treating patients with grade III or IV gliomas that have come back after a period of improvement (recurrent)....

What is the current status of trial NCT06964737?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 2025-05-21. Estimated completion is 2026-12-31.

What conditions does trial NCT06964737 study?

This clinical trial studies the following conditions: Recurrent Malignant Glioma, WHO Grade 3 Glioma, WHO Grade 4 Glioma, Recurrent WHO Grade 4 Glioma, Recurrent WHO Grade 3 Glioma.

What interventions are being tested in trial NCT06964737?

The interventions under investigation include: Biospecimen Collection (PROCEDURE), Magnetic Resonance Imaging (PROCEDURE), Echocardiography Test (PROCEDURE), Chest Radiography (PROCEDURE), Anti-GARP Chimeric Antigen Receptor-T Cells (BIOLOGICAL).

Who is sponsoring clinical trial NCT06964737?

This trial is sponsored by Ohio State University Comprehensive Cancer Center, which has 341 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06964737 being conducted?

This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Recurrent Malignant Glioma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06964737's enrollment target sits among peer trials

30 6th of 17 higher than 11 of 17 other Recurrent Malignant Glioma trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Recurrent Malignant Glioma trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06964737, the US trial registry maintained by the National Library of Medicine. NCT06964737 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.