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Study identifier: NCT06545942 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Study of Orally Administered MOMA-313 in Participants With Advanced or Metastatic Solid Tumors

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

PhasePhase 1
Planned participants220
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-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.

Talk to the study team

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

Always discuss trial participation with your own doctor first.

Locations (18)

Investigative Site #108Goodyear, Arizona, United StatesRecruiting
Investigative Site #101La Jolla, California, United StatesRecruiting
Investigative Site #111San Francisco, California, United StatesCompleted
Investigative Site #104Lake Mary, Florida, United StatesRecruiting
Investigative Site #110St Louis, Missouri, United StatesRecruiting
Investigative Site #103New York, New York, United StatesRecruiting
Investigative Site #106New York, New York, United StatesRecruiting
Investigative Site #109Philadelphia, Pennsylvania, United StatesRecruiting
Investigative Site #107Myrtle Beach, South Carolina, United StatesCompleted
Investigative Site #102Nashville, Tennessee, United StatesRecruiting
Investigative Site #105San Antonio, Texas, United StatesCompleted
Investigative Site #112Fairfax, Virginia, United StatesCompleted

+ 6 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06545942