drugset / Trial / NCT03212586

BAY 1902607: Single Dose Escalation, Safety and Tolerability, Pharmacokinetics, Bioavailability, Food Effect

NCT03212586 ↗

Phase 1 Completed 72 enrolled Bayer
RandomizedParallel-groupQuadruple-blindBasic science

Summary

This study is a first-in-man study that will investigate the safety, tolerability and pharmacokinetics of ascending single doses of BAY1902607 using a placebo controlled, randomized, single center design. In addition the influence of food on the pharmacokinetics of BAY1902607 and the bioavailability between different pharmaceutical formulations will be investigated

Timeline

Start
2017-07-18
Primary completion
2018-05-03
Completion
2018-07-27

Drugs

EvaluationDrugModalityDoseRoute
Subject BAY1902607 Unknown — Oral

Indications

No indication recorded.