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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.

Phase 1RecruitingCandid TherapeuticsNCT07215650Data as of May 2026

Treatment: CizutamigThe 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.

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Extracted 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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