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Clinical Trial Summary

This study will be conducted primarily to determine the pharmacokinetics of copanlisib in Chinese patients with relapsed iNHL.

The primary objective of the study is to determine the pharmacokinetics of copanlisib administered on Day1, 8, and 15 of a 28-days cycle (3 weeks-on/1 week off dosing regimen) as a 1 hour intravenous infusion to Chinese patients with relapsed iNHL.

The secondary objectives include the evaluation of safety, tolerability, and tumor response of Chinese patients treated with Copanlisib.

Determine the pharmacokinetics of M-1 metabolite.

Clinical Trial Description


Study Design

Related Conditions & MeSH terms

NCT number NCT03498430
Study type Interventional
Source Bayer
Contact Bayer Clinical Trials Contact
Phone (+) 1-888-8422937
Status Recruiting
Phase Phase 1
Start date April 27, 2018
Completion date April 3, 2020

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