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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.

Phase 1RecruitingCandid TherapeuticsNCT07215650Data as of Jun 2026Location: China

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

Treatments studied

Other

Cizutamig

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.

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