drugset / Trial / NCT02264015

Pharmacodynamic Effects, Safety and Tolerability of Cilobradine, to Healthy Male and Female Volunteers, With an Intra-individual Comparison to Moxifloxacin in a Subset of Volunteers

NCT02264015

Phase 1 Completed 125 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

Incidence of visual phenomena, heart rate at rest, safety (with particular emphasis on QT analysis of ECGs), and pharmacokinetic parameters

Timeline

Start
2004-01
Primary completion
2004-05
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Cilobradine Small molecule 2 mg Oral
Subject Cilobradine Small molecule 5 mg Oral
Comparator Moxifloxacin Small molecule 400 mg

Indications

No indication recorded.