Condition: Advanced Solid Tumor · Metastatic Solid Tumor · Prostate 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-313 administered orally as a single agent or combination therapy in patients with homologous recombinant deficient 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 #108 | Goodyear, Arizona, United States | Recruiting |
| Investigative Site #101 | La Jolla, California, United States | Recruiting |
| Investigative Site #111 | San Francisco, California, United States | Completed |
| Investigative Site #104 | Lake Mary, Florida, United States | Recruiting |
| Investigative Site #110 | St Louis, Missouri, United States | Recruiting |
| Investigative Site #103 | New York, New York, United States | Recruiting |
| Investigative Site #106 | New York, New York, United States | Recruiting |
| Investigative Site #109 | Philadelphia, Pennsylvania, United States | Recruiting |
| Investigative Site #107 | Myrtle Beach, South Carolina, United States | Completed |
| Investigative Site #102 | Nashville, Tennessee, United States | Recruiting |
| Investigative Site #105 | San Antonio, Texas, United States | Completed |
| Investigative Site #112 | Fairfax, Virginia, United States | Completed |
+ 6 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT06545942