Clinical Trial

Zavegepant Intranasal Spray for the Acute Treatment of Episodic Cluster Headache

Not Yet Recruiting Phase 2
View on ClinicalTrials.gov →
Summary
The purpose of this study is to assess headache response rate for minimal pain at 30 minutes following zavegepant administration and to assess additional effectiveness and treatment failure endpoints at various timepoints after zavegepant administration
Trial Details
NCT Number NCT07714369
Lead Sponsor The University of Texas Health Science Center, Houston
Collaborators: Pfizer
Conditions Cluster Headache
Enrollment 40 participants
Start Date 2026-10-01
Primary Completion 2028-04-01 (estimated)
Study Completion 2028-05-01 (estimated)
Updated on ClinicalTrials.gov 2026-07-20