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.
Treatment: mRNA-2808 — The 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 qualifyExtracted 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?
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