OncoMatch

OncoMatch/Clinical Trials/NCT07116616

A Study of mRNA-2808 in Participants With Relapsed or Refractory Multiple Myeloma

Is NCT07116616 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies mRNA-2808 for relapsed or refractory multiple myeloma.

Phase 1/2RecruitingModernaTX, Inc.NCT07116616Data as of May 2026

Treatment: mRNA-2808The purpose of this study is to evaluate the safety and tolerability of mRNA-2808 in participants with relapsed or refractory multiple myeloma (RRMM).

Check if I qualify

Extracted eligibility criteria

Cancer type

Multiple Myeloma

Prior therapy

Must have received: proteasome inhibitor

prior exposure to a proteasome inhibitor

Must have received: immunomodulatory drug

prior exposure to an immunomodulatory drug (IMiD)

Must have received: anti-CD38 monoclonal antibody

prior exposure to an anti-cluster of differentiation (CD38) monoclonal antibody

Cannot have received: radiotherapy

Exception: palliative radiotherapy of limited field is permissible within 2 weeks after discussion with the Sponsor medical monitor

Radiotherapy or cytotoxic chemotherapy within 2 weeks prior to Day 1 (Baseline)

Cannot have received: cytotoxic chemotherapy

Radiotherapy or cytotoxic chemotherapy within 2 weeks prior to Day 1 (Baseline)

Cannot have received: antibody-based immunotherapy

Antibody-based immunotherapy (monoclonal antibody, bispecific antibody, antibody drug conjugate) within 21 days prior to Day 1 (Baseline)

Cannot have received: proteasome inhibitor

Proteasome inhibitor therapy ... within 14 days prior to Day 1 (Baseline)

Cannot have received: immunomodulatory drug

immunomodulatory agent within 14 days prior to Day 1 (Baseline)

Cannot have received: autologous hematopoietic cell transplant

Autologous hematopoietic cell transplant within 100 days prior to Day 1 (Baseline)

Cannot have received: allogeneic hematopoietic cell transplant

Allogeneic hematopoietic cell transplant within 180 days prior to Day 1 (Baseline)

Cannot have received: genetically modified adoptive cellular therapy (chimeric antigen receptor T cell, chimeric antigen receptor natural killer)

Genetically modified adoptive autologous or allogeneic cellular therapy (for example, chimeric antigen receptor T cell, chimeric antigen receptor natural killer) within 12 weeks prior to Day 1 (Baseline)

Cannot have received: corticosteroid

Corticosteroid therapy ≥140 mg prednisone or equivalent cumulative dose within 14 days prior to Day 1 (Baseline)

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

US trial sites

  • University of Alabama at Birmingham Hospital · Birmingham, Alabama
  • UCSF · San Francisco, California
  • Emory University Hospital · Atlanta, Georgia
  • Mass General Brigham · Boston, Massachusetts
  • Tisch Cancer Institute at Mount Sinai · New York, New York

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

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