drugset / Trial / NCT00567086

Study to Assess the Safety, Tolerance and Efficacy of Tezampanel in Patients With Acute Migraine

NCT00567086 ↗

Phase 2 Completed 306 enrolled TorreyPines Therapeutics
RandomizedParallel-groupDouble-blindTreatment

Summary

To evaluate the effects of a single sc administration of TEZAMPANEL at one of three different dosage levels compared to placebo, employing traditional measures of efficacy and safety in the treatment of a single episode of acute migraine.

Timeline

Start
2006-10
Primary completion
—
Completion
2007-08

Drugs

EvaluationDrugModalityDoseRoute
Subject TEZAMPANEL ANHYDROUS Small molecule 40 mg Subcutaneous
Subject TEZAMPANEL ANHYDROUS Small molecule 70 mg Subcutaneous
Subject TEZAMPANEL ANHYDROUS Small molecule 100 mg Subcutaneous

Indications