OncoMatch/Clinical Trials/NCT07215650
Clinical Study of Cizutamig in Generalized Myasthenia Gravis (gMG)
Is NCT07215650 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1 trial studies Cizutamig for generalized myasthenia gravis.
Treatment: Cizutamig — The purpose of this study is to assess the safety, tolerability, PK, PD, immunogenicity, and preliminary clinical activity of Cizutamig in patients with Generalized Myasthenia Gravis.
Check if I qualifyExtracted eligibility criteria
Treatments studied
Other
Disease stage
Required: Stage MGFA CLASS II, MGFA CLASS III, MGFA CLASS IVA (MGFA)
classified as MGFA Class II-IVa
Prior therapy
Must have received: corticosteroid
disease recurrence or progression despite treatment with corticosteroids
Must have received: immunosuppressant (azathioprine, mycophenolate mofetil, tacrolimus, cyclosporine A, methotrexate)
disease recurrence or progression despite treatment with ... immunosuppressants (e.g., azathioprine, mycophenolate mofetil, tacrolimus, cyclosporine A, methotrexate)
Must have received: biologic (rituximab)
disease recurrence or progression despite treatment with ... biologics (e.g., rituximab)
Cannot have received: CAR-T cell therapy
Any history of CAR-T ... therapy targeting any antigen
Cannot have received: TCE therapy
Any history of ... TCE therapy targeting any antigen
Cannot have received: BCMA-targeted therapy
Any history of ... BCMA-targeted therapy
Cannot have received: immunosuppressive drug (not listed)
Exception: unless approved by the medical monitor
Use of any approved immunosuppressive drugs not listed here within 12 weeks or 5 half-lives (whichever is longer) before screening, unless approved by the medical monitor
Cannot have received: investigational non-biological agent
Participation in any investigational trial involving non-biological agents within 4 weeks or 5 half-lives (whichever is longer) ... before screening
Cannot have received: investigational biological agent
Participation in any investigational trial involving biological agents within 12 weeks or 5 half-lives (whichever is longer) ... before screening
Cannot have received: live vaccine
Administration of live vaccines within 4 weeks before screening
Structured fields extracted by AI. May contain errors — verify against the official protocol.
Frequently asked questions
Is NCT07215650 currently recruiting?
Yes, this trial is currently recruiting patients.
Are there prior therapy exclusions?
Yes. Prior CAR-T cell therapy, TCE therapy, BCMA-targeted therapy disqualifies patients from enrollment.
What disease stage is eligible?
Stage MGFA CLASS II or MGFA CLASS III or MGFA CLASS IVA is required.
Could you qualify for this trial?
Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.
Check if I qualify