drugset / Trial / NCT02342665

Japanese Phase Ib/II Copanlisib in Relapsed, Indolent B-cell NHL

NCT02342665

Phase 1/2 Completed 25 enrolled Bayer
NaSingle-groupOpen-labelTreatment

Summary

The primary objective of this study is to assess the safety profile of copanlisib at the recommended dose (primary endpoint). The recommended dose of copanlisib for Japanese patients will be determined in the dose escalation/safety evaluation part.

Timeline

Start
2015-04-21
Primary completion
2018-09-14
Completion
2022-02-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Copanlisib Small molecule Intravenous