Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
(PROSPECTOR) Screening Study Evaluating the Prevalence of the KIT D816V Mutation in Patients With Systemic Mast Cell Activation
NCT04811365 · View on ClinicalTrials.gov ↗
Study Summary
This is a multi-center screening study with the primary objective to determine the prevalence of KIT D816V mutation in peripheral blood in patients with evidence of systemic mast cell activation (MCA).
Conditions Studied
Interventions
- OTHER Screening
Study Locations (20)
Other
- Antwerp University Hospital UZA — Edegem
- Pitié-Salpêtrière Hospital — Paris
- CHU Toulouse — Toulouse
- Charite Universitatsmedizin Berlin — Berlin
- Medizinische Hochschule Hannover, Dept. of Dermatology and Allergy — Hanover
- Klinik fuer Dermatologie und Allergologie — München
- AOU San Giovanni di Dio e Ruggi d'Aragona University of Salerno — Salerno
- Azienda Ospedaliera Universitaria Integrata Verona — Verona
- Hospital Virgen del Valle — Toledo
- University of Basel — Basel
New York
- Roswell Park Cancer Center — Buffalo
- Albert P. Hirdt D.O. P.C. — New Paltz
- Columbia University Medical Center - Herbert Irving Comprehensive Cancer Center HICCC — New York
Alabama
- Clinical Research Center of Alabama — Birmingham
California
- Scripps Clinic Carmel Valley — San Diego
Massachusetts
- Brigham and Women's Hospital — Boston
Michigan
- University of Michigan — Ann Arbor
Minnesota
- Mayo Clinic — Rochester
North Carolina
- Duke University: Duke Allergy Asthma Airway Center — Durham
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 379 participants |
| Start Date | 2021-06-29 |
| Est. Completion | 2023-03-31 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04811365
The ClinicalTrials.gov registry entry for NCT04811365 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 379 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Blueprint Medicines Corporation, which has 9 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with KIT D816V Mutation appearing as the primary indexed condition, and to 1 intervention — of which Screening is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT04811365 reports 20 study locations spanning 9 distinct geographic areas — top geographies include Other, New York, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT04811365 about?
NCT04811365 is a clinical study titled "(PROSPECTOR) Screening Study Evaluating the Prevalence of the KIT D816V Mutation in Patients With Systemic Mast Cell Activation". This is a multi-center screening study with the primary objective to determine the prevalence of KIT D816V mutation in peripheral blood in patients with evidence of systemic mast cell activation (MCA).
What is the current status of trial NCT04811365?
This trial is currently completed. The enrollment target is 379 participants. The study started on 2021-06-29. Estimated completion is 2023-03-31.
What conditions does trial NCT04811365 study?
This clinical trial studies the following conditions: KIT D816V Mutation, Systemic Mast Cell Activation. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04811365?
The interventions under investigation include: Screening (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04811365?
This trial is sponsored by Blueprint Medicines Corporation, which has 9 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04811365 being conducted?
This trial has 20 study locations across Alabama, California, Massachusetts, Michigan, Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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