RecruitingPhase 1NCT06966024

Study of DCC-2812 in Participants With Advanced Genitourinary Cancers

An Open-label, Phase 1 Study of DCC-2812 Monotherapy in Participants With Advanced or Metastatic Renal Cell Carcinoma, Urothelial Cancer, or Castration-Resistant Prostate Cancer


Sponsor

Deciphera Pharmaceuticals, LLC

Enrollment

60 participants

Start Date

Aug 27, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This is a multicenter clinical trial to evaluate the safety and preliminary activity of the selective general control nonderepressible 2 (GCN2) activator DCC-2812 as monotherapy in advanced/metastatic renal cell carcinoma (RCC), urothelial carcinoma, and castration-resistant prostate cancer.


Eligibility

Min Age: 18 Years

Inclusion Criteria4

  • Have confirmed Advanced or Metastatic Renal Cell Carcinoma, Urothelial Cancer, or Castration-Resistant Prostate Cancer
  • Able to take oral medication
  • If a female is of childbearing potential, must have a negative pregnancy test prior to enrollment and all participants agree to follow the contraception requirements
  • Adequate organ function and electrolytes

Exclusion Criteria3

  • Received any prior anticancer therapy or any investigational therapy within a specified timeframe prior to first dose of DCC-2812
  • Impaired cardiac function
  • Major surgery within 28 days of the first dose of study drug

Interventions

DRUGDCC-2812

Administered orally


Locations(3)

Dana-Farber Cancer Institute

Boston, Massachusetts, United States

NEXT Oncology, Austin

Austin, Texas, United States

NEXT Oncology, San Antonio

San Antonio, Texas, United States

View Full Details on ClinicalTrials.gov

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NCT06966024


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