Condition: Advanced Solid Tumor · Metastatic Solid Tumor · Endometrial Cancer · Sponsor: MOMA Therapeutics
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.
MOMA Clinical Trials · 857-285-3677 · clinicaltrials@momatx.com
Always discuss trial participation with your own doctor first.
| Investigative Site #132 | Phoenix, Arizona, United States | Recruiting |
| Investigative Site #101 | San Diego, California, United States | Recruiting |
| Investigative Site #128 | Tampa, Florida, United States | Recruiting |
| Investigative Site #120 | Detroit, Michigan, United States | Recruiting |
| Investigative Site #110 | St Louis, Missouri, United States | Recruiting |
| Investigative Site #131 | Raleigh, North Carolina, United States | Recruiting |
| Investigative Site #121 | Portland, Oregon, United States | Recruiting |
| Investigative Site #127 | Dallas, Texas, United States | Completed |
| Investigative Site #129 | Houston, Texas, United States | Recruiting |
| Investigative Site #122 | Sydney, New South Wales, Australia | Recruiting |
| Investigative Site #123 | Westmead, New South Wales, Australia | Recruiting |
| Investigative Site #124 | Woolloongabba, Queensland, Australia | Completed |
+ 3 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT06974110