Study of BLU-808 in Chronic Inducible Urticaria (CIndU) and Chronic Spontaneous Urticaria (CSU)

Recruiting Phase 2 Interventional Study
Chronic Inducible Urticaria Chronic Spontaneous Urticaria
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
105 (estimated)
Sponsor
Blueprint Medicines Corporation · Industry
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About This Trial

This is a 2-part, proof-of-concept study to be conducted globally, designed to evaluate the safety, tolerability, clinical activity, pharmacokinetics, and pharmacodynamics of BLU-808, a wild type KIT inhibitor, in participants with CIndU (Part A) or CSU (Part B).

Trial Locations
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Eligibility Criteria
Key Inclusion Criteria: * Part A: Confirmed diagnosis of CIndU for ≥3 months prior to Day 1 that is inadequately controlled with second generation H1-antihistamines. * Part B: Confirmed diagnosis of CSU for ≥3 months prior to Day 1 that is inadequately controlled with second generation H1-antihista…
Contacts

Blueprint Medicines

1-888-258-7768

medinfo@blueprintmedicines.com

CONTACT

Blueprint Medicines, EU Contact

+31 85 064 4001

medinfoeurope@blueprintmedicines.com

CONTACT