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Completed Phase 3 Interventional Results available

Phase 3 Study of DCC-2618 vs Placebo in Advanced GIST Patients Who Have Been Treated With Prior Anticancer Therapies

ClinicalTrials.gov ID: NCT03353753

Public ClinicalTrials.gov record NCT03353753. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 4:40 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, INterVentional, Double-Blind, Placebo-Controlled Study to Assess the Safety and Efficacy of DCC-2618 In Patients With AdvanCed Gastrointestinal Stromal TUmorS Who Have Received Treatment With Prior Anticancer Therapies

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a 2-arm, randomized, placebo-controlled, double-blind, international, multicenter study comparing the efficacy of ripretinib (DCC-2618) to placebo in patients who have received treatment with prior anticancer therapies. Prior anticancer therapies must include imatinib, sunitinib, and regorafenib (3 prior therapies). Approximately 120 patients were randomized in a 2:1 ratio to ripretinib 150 mg QD or placebo

Study identification

NCT ID
NCT03353753
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Deciphera Pharmaceuticals, LLC
Industry
Enrollment
129 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 27, 2018 (Actual)
Primary completion
May 31, 2019 (Actual)
Completion
May 11, 2022 (Actual)
Last update posted
Nov 21, 2022

2018 – 2022

United States locations

U.S. sites
15
U.S. states
11
U.S. cities
13
Facility City State ZIP Site status
HonorHealth Scottsdale Arizona 85260 —
University of Southern California - Norris Los Angeles California 90033 —
UCLA Los Angeles California 90095 —
Stanford Stanford California 94305 —
Mayo Clinic - Jacksonville Jacksonville Florida 32224 —
Georgia Cancer Specialists Atlanta Georgia 30341 —
University of Chicago Chicago Illinois 60637 —
Dana Farber Cancer Institute Boston Massachusetts 02215 —
University of Minnesota Minneapolis Minnesota 55455 —
Mayo Clinic Rochester Minnesota 55905 —
Columbia New York New York 10027 —
MSKCC New York New York 10065 —
Oregon Health & Science University Portland Oregon 97239 —
Fox Chase Cancer Center Philadelphia Pennsylvania 19111 —
MD Anderson Cancer Center Houston Texas 77030 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 20 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03353753, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 21, 2022 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03353753 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →