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Spots Global Cancer Trial Database for A Study of DCC-2701 in Participants With Advanced Solid Tumors

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Trial Identification

Brief Title: A Study of DCC-2701 in Participants With Advanced Solid Tumors

Official Title: A Multicenter Phase 1 Ascending Dose Study of DCC-2701 To Assess Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics in Patients With Advanced Solid Tumors

Study ID: NCT02228811

Interventions

DCC-2701 tablet

Study Description

Brief Summary: The main purpose of this study is to investigate the safety of the investigational drug DCC-2701 and whether it will work to help people who have advanced solid tumors or cancer that has spread to other parts of the body.

Detailed Description: This is a first-in-human study of DCC-2701. The primary purpose of this study is to determine what dose of DCC-2701, can be given safely to patients with advanced solid tumors. The study will have two phases. The first phase will assess escalating doses of DCC-2701 in order to determine the maximally tolerated dose (MTD) and the optimal dosing regimen (ODR) of DCC-2701. Once the MTD and ODR is established, a dose expansion phase will further evaluate the safety of DCC-2701, as well as the activity of DCC-2701 in select solid tumor types.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University of Colorado Hospital, Aurora, Colorado, United States

Massachusetts General Hospital, Boston, Massachusetts, United States

The Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, United States

Vanderbilt University Medical Center, Nashville, Tennessee, United States

MD Anderson Cancer Center, Houston, Texas, United States

Contact Details

Name: Oliver Rosen, M.D.

Affiliation: Deciphera Pharmaceuticals LLC

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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