Skip to content
Trial Eligibility
Menu

Study of Oral MRT-2359 With Apalutamide in Prostate Cancer

NCT07745361

This study is recruiting at 5 US sites in 5 states, according to its ClinicalTrials.gov record last updated .

Summary

This Phase 2, open-label, multicenter study is conducted in patients with castration-resistant prostate cancer. Patients in this study receive MRT-2359, an investigational oral medicine, in combination with apalutamide, an oral medicine used to treat prostate cancer. The main purpose of the study is to assess whether this treatment combination can lower prostate-specific antigen (PSA) The study will also evaluate the safety and tolerability of the treatment combination and assess additional measures of anti-tumor activity.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Castration-Resistant Prostate Cancer (CRPC)
  • Castration-Resistant Prostate Cancer
  • Prostate Cancer
  • Prostate Cancer (Adenocarcinoma)

Eligibility basics and study details

Study type
Interventional
Phase
Phase 2
Ages
18 years and older
Sex
Male
Healthy volunteers
Not accepted
Sponsor
Monte Rosa Therapeutics, Inc
Last updated on ClinicalTrials.gov
October 8, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

California · 1

  • START Los Angeles · Los Angeles, CA

Nebraska · 1

  • XCancer Omaha · Omaha, NE

New Jersey · 1

  • START New Jersey · East Brunswick, NJ

Utah · 1

  • START Mountain Region · West Valley City, UT

Washington · 1

  • University of Washington Medical Center · Seattle, WA

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.