drugset / Trial / NCT02137733

The Cardiac Insufficiency BIsoprolol Study in Japanese Patients With Chronic Heart Failure (CIBIS-J)

NCT02137733

Unknown 220 enrolled Mebix Inc
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to investigate the non-inferiority of bisoprolol to carvedilol by evaluating tolerability (The probability that administered maintenance dose reaches the maximum will be determined as an indicator) as a primary endpoint when bisoprolol or carvedilol is administered for 48 weeks to Japanese chronic heart failure patients. In addition, the safety and efficacy of bisoprolol will be investigated.

Timeline

Start
2013-06
Primary completion
2016-05
Completion

Drugs

EvaluationDrugModalityDoseRoute
Comparator Bisoprolol Other / unclassified 5 mg Oral
Comparator Carvedilol Other / unclassified 20 mg Oral

Indications