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OncoMatch/Clinical Trials/NCT07105059

A Study of Teclistamab and Mezigdomide in People With Multiple Myeloma

Is NCT07105059 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies multiple treatments including Teclistamab and Mezigdomide for multiple myeloma.

Phase 1RecruitingMemorial Sloan Kettering Cancer CenterNCT07105059Data as of May 2026

Treatment: Teclistamab · MezigdomideThe researchers are doing this study to find out whether combining teclistamab and mezigdomide is a safe and effective treatment approach in people with relapsed/refractory multiple myeloma (MM).

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Extracted eligibility criteria

Cancer type

Multiple Myeloma

Biomarker criteria

Required: BCMA cell surface expression (presence confirmed in patients with prior BCMA targeted therapy)

BCMA presence on the cell surface should be confirmed in patients who have been treated with prior BCMA targeted therapies.

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Min 2 prior lines

Must have received: proteasome inhibitor

Patients with relapsed or refractory multiple myeloma who have been treated with a proteasome inhibitor

Must have received: IMiD

Patients with relapsed or refractory multiple myeloma who have been treated with...an IMiD

Must have received: anti-CD38 antibody

Patients with relapsed or refractory multiple myeloma who have been treated with...an anti-CD38 antibody

Cannot have received: BCMA targeted bispecific antibody

Prior treatment with a BCMA targeted bispecific antibody

Cannot have received: mezigdomide (mezigdomide)

Prior treatment with mezigdomide

Cannot have received: systemic anti-myeloma therapy

Exception: within ≤14 days

Systemic anti-myeloma therapy (including systemic steroids) within ≤14 days, or plasmapheresis within 7 days prior to the first dose of study drug.

Cannot have received: investigational drug

Exception: within 21 days or five half-lives (whichever is longer)

Use of an investigational drug within 21 days or five half-lives (whichever is longer) preceding the first dose of study drug.

Cannot have received: radiation therapy

Exception: within ≤14 days prior to study entry (bone lesions requiring radiation may be treated with limited [i.e., ≤ 25% of bone marrow in field] radiation therapy during this period)

Radiation therapy within ≤14 days prior to study entry

Cannot have received: live, attenuated vaccine or investigational vaccine

Exception: within 4 weeks before the first dose of study drug

Live, attenuated vaccine or investigational vaccine within 4 weeks before the first dose of study drug

Cannot have received: autologous stem cell transplant

Exception: within 60 days

Patients with a history of autologous stem cell transplant within 60 days

Cannot have received: allogeneic stem cell transplant

Exception: within 6 months prior to study enrollment

allogeneic stem cell transplant within 6 months prior to study enrollment

Cannot have received: CAR-T cell therapy

Exception: within 90 days prior to study enrollment

Patients who received CAR T therapy within 90 days prior to study enrollment

Lab requirements

Blood counts

Hemoglobin ≥8 g/dL (no transfusion within 7 days); ANC ≥1.0 × 10^9/L (no growth factor support within 7 days for G-CSF/GM-CSF, 14 days for pegylated-G-CSF); Platelets ≥75 × 10^9/L (<50% plasma cells) or ≥50 × 10^9/L (≥50% plasma cells) (no transfusion/thrombopoietin receptor agonist within 7 days)

Kidney function

eGFR ≥30 mL/min (CKD-EPI formula)

Liver function

Total bilirubin ≤2 × ULN (except Gilbert syndrome); AST and ALT ≤2.5 × ULN

Fulfil the criteria for Adequate Organ System Function Based on Safety Assessments

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Memorial Sloan Kettering Basking Ridge (Limited Protocol Activities) · Basking Ridge, New Jersey
  • Memorial Sloan Kettering Monmouth (Limited Protocol Activities) · Middletown, New Jersey
  • Memorial Sloan Kettering Bergen (Limited Protocol Activities) · Montvale, New Jersey
  • Memorial Sloan Kettering Suffolk - Commack (Limited Protocol Activities) · Commack, New York
  • Memorial Sloan Kettering Westchester (Limited Protocol Activities) · Harrison, New York

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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