Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT07364487

This is an Open-Label Study to Assess the Safety and Efficacy of GC012F in Patients With Multiple Sclerosis

An Open-Label Study to Assess the Safety and Efficacy of GC012F in Patients With Multiple Sclerosis

Status
Withdrawn
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Huashan Hospital · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This is an open-label,early-stage exploratory clinical study to evaluate the safety and preliminary efficacy of GC012F CAR T cell injection in Multiple Sclerosis subjects.

Detailed description

This is a single-arm, open-label, early exploratory clinical study to evaluate the safety and efficacy of GC012F Injection in subjects with MS, as well as to assess its PK and PD profiles. This study consists of the following periods: screening period, apheresis day, baseline period, lymphodepletion preconditioning period, GC012F infusion, safety and efficacy follow-up period, and long-term follow-up period. In this study, a single dose group is planned for the CAR-T cell infusion dose,and 15 evaluable subjects will be included. Eligible subjects will receive a single infusion of GC012F Injection and will be monitored for DLTs within 28 days following the infusion of GC012F Injection. After all the 6 subjects have completed DLT observation, all clinical study safety data collected during the DLT observation phase will be assessed. 9 subjects will be enrolled in the dose expansion phase. After CAR-T cell infusion, subjects will be followed up for safety, cell proliferation and survival, and efficacy until 672 days (96 weeks) after infusion, withdrawal from the study, death, withdrawal of informed consent, or lost to follow-up, whichever occurs first.

Conditions

Interventions

TypeNameDescription
DRUGGC012F CAR-T Cell InjectionA single dose group is planned for the CAR-T cell infusion dose is administrated for each subject.Single IV infusion.

Timeline

Start date
2026-01-26
Primary completion
2026-03-25
Completion
2026-03-25
First posted
2026-01-23
Last updated
2026-03-30

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07364487. Inclusion in this directory is not an endorsement.