drugset / Trial / NCT02367313

A Phase 2 Study of Vapendavir in Asthmatic Adults With Symptomatic Human Rhinovirus Infection

NCT02367313 ↗

Phase 2 Completed 455 enrolled Biota Pharmaceuticals, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This Phase 2 protocol is designed to compare two dose levels of Vapendavir versus placebo. The objectives are to obtain safety and efficacy data in moderate to severe asthmatic patients, aged 18 to 75 years at risk of loss of asthma control due to presumptive Human Rhinovirus infection.

Timeline

Start
2015-02
Primary completion
2016-12
Completion
2016-12

Drugs

EvaluationDrugModalityDoseRoute
Comparator Vapendavir Small molecule 264 mg —
Comparator Vapendavir Small molecule 528 mg —

Indications