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Clinical Trial Summary

This is a 3 part study for patients with solid tumours. The purpose of Part A is to measure the amount of olaparib or its breakdown products in the bloodstream for up to 72 hours after eating and the effect of olaparib on QT interval following a single oral dose of olaparib tablets. Part B will determine the effect of olaparib on the QT interval following multiple oral dosing. Part C will allow patients continued access to olaparib tablets and will provide additional safety data collection.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01921140
Study type Interventional
Source AstraZeneca
Contact
Status Completed
Phase Phase 1
Start date September 24, 2013
Completion date March 15, 2022

See also
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