CI

At a glance

ClinicalIndex Comparison Record
Phase 1Recruiting· 48 target
Drug / intervention
B7-H3-CAR T cellsdrug
Likely dose
Not stated in record
Key inclusion· 14
  • Age ≤21 years
  • Primary CNS tumor
  • Relapsed or refractory non-brainstem CNS tumor (Cohort A)
  • Diffuse midline glioma (Cohort B)
Key exclusion· 11
  • Primary immunodeficiency or acquired immunodeficiency
  • HIV positive
  • Severe intercurrent bacterial, viral, or fungal infection
  • Rapidly progressive disease

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05835687
NCT05835687Phase 1RecruitingOn Track
Long Recruiting

Loc3CAR: Locoregional Delivery of B7-H3-specific Chimeric Antigen Receptor Autologous T Cells for Pediatric Patients With Primary CNS Tumors

St. Jude Children's Research Hospital·interventional·Posted Apr 28, 2023·Updated May 5, 2026

In Brief

A Phase 1 clinical trial evaluating B7-H3-CAR T cells for Central Nervous System Neoplasms and 6 related conditions. Currently recruiting, targeting 48 participants across 1 site.

Detailed Summary

Loc3CAR is a Phase I clinical trial evaluating the use of autologous B7-H3-CAR T cells for participants ≤ 21 years old with primary CNS neoplasms. B7-H3-CAR T cells will be locoregionally administered via a CNS reservoir catheter. Study participants will be divided into two cohorts: cohort A with B7-H3-positive relapsed/refractory non-brainstem primary CNS tumors, and cohort B with diffuse midline gliomas (DMG). Participants will receive four (4) B7-H3-CAR T cell infusions over a 4 week period. The purpose of this study is to find the maximum (highest) dose of B7-H3-CAR T cells that are safe to give patients with primary brain tumors. Primary objectives * To determine the safety, maximum tolerated dose (MTD) and recommended phase 2 dose (RP2D) for the locoregional delivery of autologous B7-H3-CAR T cells in patients ≤ 21 years of age with recurrent/refractory B7-H3+ primary CNS tumors (Cohort A) or DMG (Cohort B). Secondary objectives * To assess the efficacy, defined as sustained objective response, a partial response (PR) or complete response (CR) observed anytime on active treatment with B7-H3-CAR T cells in patients with relapsed/refractory B7-H3+ primary CNS tumors (Cohort A) or DMG (Cohort B). * To characterize and monitor neurologic toxicities in patients while on study (Cohort A and B).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 1Recruiting
20242025202620272028
First PostedApr 28, 2023
Enrollment StartApr 27, 2023
Primary CompletionMar 1, 2028
TodayJul 2, 2026
Enrollment to primary: 4.8 yearsPosted 3.2 years agoPrimary completion in 1.7 years

Interventions

B7-H3-CAR T cellsdrug

Autologous T cells transduced with a lentiviral vector expressing a B7-H3-CAR with a CD28z signaling domain and 41BB ligand (B7-H3-CAR T cells). Four (4) infusions of B7-H3-CAR T cells will be locoregionally administered via CNS reservoir catheter.