drugset / Trial / NCT03172884

Study of Copanlisib in Hepatic or Renal Impairment

NCT03172884

Phase 1 Completed 30 enrolled Bayer
Non-randomizedParallel-groupOpen-labelOther

Summary

To evaluate the pharmacokinetics and safety of copanlisib in subjects with impaired hepatic or renal function in comparison to healthy subjects

Timeline

Start
2017-06-14
Primary completion
2020-03-13
Completion
2020-05-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Copanlisib Small molecule 12 mg Intravenous

Indications