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NCT07116616

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

Recruiting now Phase 1, PHASE2 Last updated 3 April 2026
What this trial tests

Phase 1, PHASE2 trial testing mRNA-2808 in Relapsed or Refractory Multiple Myeloma in 166 participants. Currently enrolling.

Timeline
30 September 2025
Primary endpoint
17 June 2030
17 June 2032

Quick facts

Lead sponsorModernaTX, Inc.
PhasePhase 1, PHASE2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment166
Start date30 September 2025
Primary completion17 June 2030
Estimated completion17 June 2032
Sites10 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

ModernaTX, Inc. — full company profile →

Who can join

18 and older, any sex, with Relapsed or Refractory Multiple Myeloma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. RNA-Based Therapeutic Strategies in Multiple Myeloma: From Molecular Targets to Delivery and Clinical Translation.
    Baranov MV, Shalik I, Tsvetkova A, Streltsova A, et al · · 2026 · cited 1× · PMID 41596492 · DOI 10.3390/ijms27020843

Verify or expand the search:

Other recruiting trials for Relapsed or Refractory Multiple Myeloma

Currently open trials in the same condition.

Other ModernaTX, Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07116616.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing