OncoMatch/Clinical Trials/NCT07215650
Clinical Study of Cizutamig in Generalized Myasthenia Gravis (gMG)
Is NCT07215650 recruiting? Yes, currently enrolling (May 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
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.
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