drugset / Trial / NCT01412736

A Phase IIa Study of KHK4563

NCT01412736 ↗

Phase 2 Completed 106 enrolled Kyowa Kirin, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a double-blind, placebo-controlled dose-ranging study of KHK4563 to evaluate the effect of multiple-dose subcutaneous administration of KHK4563 on the annual asthma exacerbation rate in adult subjects with uncontrolled, suspected eosinophilic asthma.

Timeline

Start
2011-08
Primary completion
2013-07
Completion
2013-10

Drugs

EvaluationDrugModalityDoseRoute
Subject KHK4563 Unknown 2 mg Subcutaneous
Subject KHK4563 Unknown 20 mg Subcutaneous
Subject KHK4563 Unknown 100 mg Subcutaneous

Indications