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Study identifier: NCT06974110 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Study of Orally Administered MOMA-341 in Participants With Advanced or Metastatic Solid Tumors

Condition: Advanced Solid Tumor · Metastatic Solid Tumor · Endometrial Cancer  ·  Sponsor: MOMA Therapeutics

PhasePhase 1
Planned participants132
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This Phase 1, multi-center, open-label, dose escalation and dose optimization study is designed to assess the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PDx), and preliminary clinical activity of MOMA-341 administered orally as a single agent or combination therapy in patients with microsatellite instability high (MSI-H) or DNA mismatch repair deficiency (dMMR) solid tumors.

This description comes directly from the study's public registry record.

Talk to the study team

MOMA Clinical Trials  ·  857-285-3677  ·  clinicaltrials@momatx.com

Always discuss trial participation with your own doctor first.

Locations (15)

Investigative Site #132Phoenix, Arizona, United StatesRecruiting
Investigative Site #101San Diego, California, United StatesRecruiting
Investigative Site #128Tampa, Florida, United StatesRecruiting
Investigative Site #120Detroit, Michigan, United StatesRecruiting
Investigative Site #110St Louis, Missouri, United StatesRecruiting
Investigative Site #131Raleigh, North Carolina, United StatesRecruiting
Investigative Site #121Portland, Oregon, United StatesRecruiting
Investigative Site #127Dallas, Texas, United StatesCompleted
Investigative Site #129Houston, Texas, United StatesRecruiting
Investigative Site #122Sydney, New South Wales, AustraliaRecruiting
Investigative Site #123Westmead, New South Wales, AustraliaRecruiting
Investigative Site #124Woolloongabba, Queensland, AustraliaCompleted

+ 3 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06974110