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Clinical Trial Summary

A Phase Ib, open label, non randomized study to measure the safety and PK characteristics of APL-1202 at steady-state in adult male and female BCG resistant NMIBC patients when it is administered alone and concurrently with BCG.


Clinical Trial Description

Six eligible participants will be administered with APL-1202 one week prior to the first BCG instillation, during the six-week course of BCG instillation, and additional five weeks, for a total of 12 weeks of dosing. Safety assessment will be performed during the entire 13 week study duration. Plasma and urine samples will be collected from each participant at prior to first and fifth BCG instillations for PK analysis. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03672240
Study type Interventional
Source AsierisPharma
Contact
Status Completed
Phase Phase 1/Phase 2
Start date November 30, 2018
Completion date June 30, 2020

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