Drugs / BLU-808
last change Sep 2025 re-read 3 minutes ago

BLU-808

targets KIT via inhibition

Developed for
allergic disease · chronic inducible urticaria
Investigated by
Blueprint Medicines Corporation

Trials 3

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 11 trial · 1 met primary
Phase 1 NCT06948032 Aug 2024 → Jan 2025 — Blueprint Medicines Corporation Completed Met primary
Phase 22 trials
Phase 2 NCT06931405 May 2025 → Dec 2026 expected chronic inducible urticaria Blueprint Medicines Corporation Recruiting No outcome recorded
Phase 2 NCT06922448 Apr → Sep 2025 allergic disease Blueprint Medicines Corporation Completed No outcome recorded

News releases announcing trial results or a regulatory action · 2

DateIssuerRelease
2025-02-28 Blueprint Medicines Corporation Results Blueprint Medicines Highlights Leading Portfolio of Mast Cell-Targeted Therapies at 2025 AAAAI / WAO Joint Congress blueprintmedicines.com ↗
BLU-808 healthy volunteer trial results demonstrate wide therapeutic window for modulating mast cell activity, affirming potential as best- and first-in-class oral wild-type KIT inhibitor
2025-01-12 Blueprint Medicines Corporation Results Blueprint Medicines Provides 2025 Outlook and Highlights Strategy for Continued Growth blueprintmedicines.com ↗
BLU-808 demonstrates wide therapeutic window with rapid, robust and sustained tryptase reductions exceeding 80% in Phase 1 healthy volunteer study

All press releases naming this drug 2 releases

DateIssuerRelease

Evidence & citations 4 cited values

Every value below carries the sentence it was read from. 3 sources stand behind the page.

FieldValueCited text
Known as BLU-808 ClinicalTrials.gov intervention name — accepted as the source's own label NCT06931405 ↗
2

NCT06922448 ↗

NCT06948032 ↗

Action Inhibit “Wild-type KIT Inhibitor” NCT06922448 ↗
Route Oral “BLU-808 will be administered orally for 28 days.” NCT06922448 ↗
Target KIT “Wild-type KIT Inhibitor” NCT06922448 ↗