drugset / Trial / NCT06922448

Study of BLU-808 in Allergic Rhinoconjunctivitis

NCT06922448 ↗

Phase 2 Completed 21 enrolled Blueprint Medicines Corporation
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study will evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary clinical activity of BLU-808 in participants with ragweed (Ambrosia artemisiifolia)-induced allergic rhinoconjunctivitis (ARC). Participants will undergo eligibility assessments that include exposure to ragweed pollen in an allergen exposure chamber (AEC).

Timeline

Start
2025-04-14
Primary completion
2025-09-08
Completion
2025-09-08

Drugs

EvaluationDrugModalityDoseRoute
Subject BLU-808 Unknown — Oral

Indications