ClinicalTrials.gov record
Active, not recruiting Phase 2 Interventional

(PIONEER) Study to Evaluate Efficacy and Safety of Avapritinib (BLU-285), A Selective KIT Mutation-targeted Tyrosine Kinase Inhibitor, Versus Placebo in Patients With Indolent Systemic Mastocytosis

ClinicalTrials.gov ID: NCT03731260

Public ClinicalTrials.gov record NCT03731260. 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 Apr 22, 2026, 8:59 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 3-Part, Randomized, Double-Blind, Placebo-Controlled Phase 2 Study to Evaluate Safety and Efficacy of Avapritinib (BLU-285), a Selective KIT Mutation-Targeted Tyrosine Kinase Inhibitor, in Indolent and Smoldering Systemic Mastocytosis With Symptoms Inadequately Controlled With Standard Therapy

Study identification

NCT ID
NCT03731260
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Blueprint Medicines Corporation
Industry
Enrollment
251 participants

Conditions and interventions

Interventions

  • Avapritinib Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Not listed

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

Study timeline

Start date
Apr 15, 2019
Primary completion
Jun 22, 2027
Completion
Jun 22, 2027
Last update posted
Sep 22, 2025

2019 – 2027

United States locations

U.S. sites
19
U.S. states
17
U.S. cities
18
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35294
Mayo Clinic Hospital Phoenix Arizona 85054
Stanford Cancer Institute Stanford California 94305
Mayo Clinic Florida Jacksonville Florida 32224
H. Lee Moffitt Cancer Center Tampa Florida 33612
Winship Cancer Institute, Emory University Atlanta Georgia 30322
Rush University Medical Center Chicago Illinois 60612
University of Kansas Hospital Kansas City Kansas 66160
Brigham & Women's Hospital Boston Massachusetts 02115
Dana Farber Cancer Institute Boston Massachusetts 02215
Michigan Medicine, University of Michigan Ann Arbor Michigan 48106
Mayo Clinic Rochester Minnesota 55905
Washington University School of Medicine St Louis Missouri 63110
Herbert Irving Comprehensive Cancer Center New York New York 10032
Duke University Health System (DUHS) Durham North Carolina 27710
University Hospitals Cleveland Medical Center Cleveland Ohio 44106
University of Texas, MD Anderson Cancer Center Houston Texas 77030
Huntsman Cancer Institute Salt Lake City Utah 84112
Virginia Commonwealth University Medical Center Richmond Virginia 23298

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 30 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03731260, 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 Sep 22, 2025 · Synced Apr 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03731260 live on ClinicalTrials.gov.

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