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Clinical Trial Summary

This study is a single-center, open-label, single-arm, dose-exploration study to evaluate the safety and preliminary effectiveness of CD19-BCMA CAR-T in the treatment of refractory, generalized myasthenia gravis. The study is a dose escalation trial in adult, refractory, systemic MG patients. The Keyboard method will be used to perform dose escalation to explore the maximum tolerated dose (MTD). A total of 12 MG patients who meet the inclusion criteria are expected to be recruited.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06371040
Study type Interventional
Source Tang-Du Hospital
Contact
Status Not yet recruiting
Phase Phase 1
Start date May 1, 2024
Completion date December 1, 2026

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