An Observational Study in Participants With Indolent Systemic Mastocytosis (ISM)

Recruiting Observational Study
Indolent Systemic Mastocytosis
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
150 (estimated)
Sponsor
Blueprint Medicines Corporation · Industry
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About This Trial
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 partic…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * 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. Exclu…
Contacts

Blueprint Medicines

1-888-258-7768

medinfo@blueprintmedicines.com

CONTACT

Blueprint Medicines, EU Contact

+31 85 064 4001

medinfoeurope@blueprintmedicines.com

CONTACT