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Clinical Trials in the UK / NCT03731260
Active, not recruiting Phase 2

(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

NCT03731260 · tracked via the Priya Life Science UK tracker
Sponsor
Blueprint Medicines Corporation
Phase
Phase 2
Started
2019-04-16
Last updated
2025-09-23

Condition(s) studied

Indolent Systemic Mastocytosis

Investigational drug(s) / intervention(s)

AvapritinibPlacebo

Avapritinib: Avapritinib tablet

Placebo: Placebo tablet

Study summary

This is a Phase 2, randomized, double-blind, placebo-controlled study comparing the efficacy and safety of avapritinib + best supportive care (BSC) with placebo + BSC in patients with indolent systemic mastocytosis (ISM) whose symptoms are not adequately controlled by BSC. The study will be conducted in 3 parts. All patients will receive treatment with avapritinib during Part 3 including those rolling over from the placebo group.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Key Inclusion Criteria: * 1\. Patient must have SM, confirmed by Central Pathology Review of BM biopsy, and central review of B- and C-findings by WHO diagnostic criteria. * 2\. Patient must have moderate-to-severe symptoms based on minimum mean total symptom score (TSS) of the ISM Symptom Assessment Form (ISM-SAF) over the 14-day eligibility screening period. * 3\. Patient must have failed to achieve adequate symptom control for 1 or more Baseline symptoms. * 4\. For patients receiving corticosteroids, the dose must be ≤ 20 mg/d prednisone or equivalent, and the dose must be stable for ≥ 14 days. * 5\. Patient must have an Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 to 2. Key Exclusion Criteria: * 1\. Patient has been diagnosed with any of the following WHO SM subclassifications: cutaneous mastocytosis only, smoldering SM, SM with associated hematologic neoplasm, aggressive SM, mast cell leukemia, or mast cell sarcoma. * 2\. Patient must not have received prior treatment with avapritinib. * 3\. Patient must not have had any cytoreductive therapy including but not limited to masitinib and midostaurin, or investigational agent for \< 14 days or 5 half-lives of the drug (whichever is longer), and for cladribine, interferon alpha, pegylated interferon, or antibody therapy \< 28 days or 5 half-lives of the drug (whichever is longer), before beginning the 14-day ISM-SAF eligibility TSS assessment. * 4\. Patient must not have received radiotherapy or psoralen and ultraviolet A (PUVA) therapy \< 14 days before beginning the 14-day ISM-SAF eligibility TSS assessment. * 5\. Patient must not have received any hematopoietic growth factor the preceding 14 days before beginning the 14-day ISM-SAF eligibility TSS assessment. * 6\. Patient must not have a QT interval corrected using Fridericia's formula (QTcF) of \> 480 msec.

Primary outcome measure(s)

Trial sites (49)

FacilityCityRegionStatus
University of Alabama at Birmingham Birmingham Alabama
Mayo Clinic Hospital Phoenix Arizona
Stanford Cancer Institute Stanford California
Mayo Clinic Florida Jacksonville Florida
H. Lee Moffitt Cancer Center Tampa Florida
Winship Cancer Institute, Emory University Atlanta Georgia
Rush University Medical Center Chicago Illinois
University of Kansas Hospital Kansas City Kansas
Brigham & Women's Hospital Boston Massachusetts
Dana Farber Cancer Institute Boston Massachusetts
Michigan Medicine, University of Michigan Ann Arbor Michigan
Mayo Clinic Rochester Minnesota
Washington University School of Medicine St Louis Missouri
Herbert Irving Comprehensive Cancer Center New York New York
Duke University Health System (DUHS) Durham North Carolina
University Hospitals Cleveland Medical Center Cleveland Ohio
University of Texas, MD Anderson Cancer Center Houston Texas
Huntsman Cancer Institute Salt Lake City Utah
Virginia Commonwealth University Medical Center Richmond Virginia
University Hospital Antwerp Edegem Belgium
Tom Baker Cancer Centre Calgary Alberta
University of Alberta Hospital Edmonton Alberta
St. Michael's Hospital Toronto Ontario
Odense Universitetshospital, ORCA/Allergicentret, Hudafdeling I og Allergicenter Odense Denmark
Hôpital de la Timone, Service de dermatologie Marseille France
Hôpital Pitié-Salpêtrière, Service de Dermatologie Paris France
CHU Toulouse Larrey, CEREMAST, Service de Dermatologie et Allergologie cutanée Toulouse France
Uniklinik RWTH Aachen Aachen Germany
Charité Universitätsmedizin Berlin Berlin Germany
University Clinic Hamburg Eppendorf, University Cancer Center Hamburg (UCCH) Hamburg Germany
Universitätsklinikum Schleswig-Holstein, Hämatologie/Onkologie Lübeck Germany
Universitätsklinik Mainz, Universitäts-Hautklinik, Clinical Research Center Mainz Germany
Universitätsmedizin Mannheim, III. Medizinische Klinik Mannheim Germany
Klinikum rechts der Isar, Technische Universität München Munich Germany
A.O.U di Bologna - IRCCS, Istituto di Ematologia Lorenzo e Ariosto Seragnoli, Ematologia Bologna Italy
Fondazione IRCCS Ca' Granda Ospedale Maggiore Poloclinico, UOC Ematologia Milan Italy
A.O. OO.RR. S.Giovanni di Dio e Ruggi d'Aragona, University of Salerno Salerno Italy
Azienda Ospedaliera Universitaria Integrata di Verona Verona Italy
University Medical Center Groningen (UMCG) Groningen Netherlands
Erasmus Medical Center Rotterdam Netherlands

+ 9 more sites — see the full list on the official registry below.

More Blueprint Medicines Corporation trials in the UK

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03731260 on ClinicalTrials.gov ↗ ← All trials in the UK