Anaphylaxis Clinical Trials

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An Observational Study in Patients With Indolent Systemic Mastocytosis

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

This is a Phase 4, non-interventional, observational study to collect detailed data on the clinical characteristics, clinical outcomes and medical management of ISM in real-world settings. The study will describe the demographic and clinical characteristics of ISM participants, including anaphylaxis and bone manifestations in ISM. Quality of life and disease control will be assessed through participant questionnaires. The study will also evaluate real world ISM treatment management, including use of avapritinib.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Male or female adult participants (≥ 18 years of age) with a diagnosis of ISM according to the World Health Organization (WHO) diagnostic criteria

• Participant is currently being treated or plans to be treated with symptom-directed therapies and/or avapritinib for ISM.

Locations
United States
Massachusetts
Brigham and Women's Allergy and Clinical Immunology, Mass General Brigham Healthcare Center (Chestnut Hill)
RECRUITING
Chestnut Hill
Contact Information
Primary
Blueprint Medicines
medinfo@blueprintmedicines.com
1-888-258-7768
Backup
Blueprint Medicines, EU Contact
medinfoeurope@blueprintmedicines.com
+31 85 064 4001
Time Frame
Start Date: 2026-04-15
Estimated Completion Date: 2032-12-01
Participants
Target number of participants: 150
Treatments
Participants With ISM
Patients who are currently being treated or plan to be treated for ISM
Sponsors
Leads: Blueprint Medicines Corporation

This content was sourced from clinicaltrials.gov