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Recruiting Phase 1 NCT06966024

Study of DCC-2812 in Participants With Advanced Genitourinary Cancers

Phase 1 – testing safety in a small group of people
Conditions: Renal Cell Carcinoma Urothelial Carcinoma Castration-resistant Prostate Cancer

Sponsor: Deciphera Pharmaceuticals, LLC

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Overview
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.
Who can participate
Key Inclusion Criteria: * 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 Key Exclusion Criteria: * 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
DCC-2812
DRUG
Locations 4
United States (4)
NEXT Oncology, Austin
Austin , Texas
Dana-Farber Cancer Institute
Boston , Massachusetts
Vanderbilt- Ingram Cancer Center
Nashville , Tennessee
Vanderbilt- Ingram Cancer Center Clinical Trials Office (CTO)
NEXT Oncology, San Antonio
San Antonio , Texas
Technical details
Status
Recruiting
Phase
Phase 1
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
27.08.2025
Completion date
01.02.2029
Registry ID
NCT06966024
Source
clinicaltrials.gov
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