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Open-label Study to Evaluate the Safety of Various Dosing Regimens of MuSK-CAART for MuSK Myasthenia Gravis

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NCT05451212

Sponsored by Cabaletta Bio (industry) · CABA — their whole pipeline →.

Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Na · None · Treatment
Enrollment
7actual
Sites
5
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2022-11-23actualWhen the study began enrolling
Primary completion2025-07-24actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-07-24actualThe whole study's end, after follow-up
First posted2022-07-11actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-11-10actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • MuSK Myasthenia Gravis

Intervention

  • Biological: MuSK-CAART

Primary outcome

what the primary-completion date above is the date OF
Adverse events
measured 3 months

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