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

Recruiting now · Phase 1

Conditions studied: Advanced Solid Tumor, Metastatic Solid Tumor, Prostate Cancer, Pancreas Cancer, Breast Cancer, Ovarian Cancer, Homologous Recombination Deficiency

In brief

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.

Key facts

Study ID
NCT06545942
Run by
MOMA Therapeutics
People needed
220
Starts
2024-08-13
Expected to finish
2027-11-30
Last updated by the study team
2026-07-23

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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