drugset / Trial / NCT04804033

A Study to Evaluate the Efficacy and Safety of Oral Zavegepant in Migraine Prevention

NCT04804033 ↗

Phase 2/3 Terminated 1753 enrolled Pfizer
RandomizedSequentialQuadruple-blindPrevention

Summary

The purpose of this is study is to compare the efficacy of BHV-3500 (zavegepant) to placebo as a preventive treatment for migraine, as measured by the reduction in the number of migraine days per month.

Timeline

Start
2021-03-26
Primary completion
2024-03-21
Completion
2024-03-21

Outcome

Outcome not reported

Stopped (Business): “Strategic decision to discontinue the study based on adjusted clinical development plan. This decision is not based on any safety concerns.”

Drugs

EvaluationDrugModalityDoseRoute
Comparator Zavegepant Small molecule 100 mg Oral
Comparator Zavegepant Small molecule 200 mg Oral

Indications