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Clinical Trial Summary

To assess the mass balance recovery after a single oral dose of 14C-AB1010


Clinical Trial Description

The objective is to characterize the distribution, metabolism and elimination of AB1010 in humans through the sampling of blood, urine, and faeces. This is accomplished through the administration of 14C-AB1010 oral solution with a therapeutic relevant dose of AB1010 as a single oral dose. There was no control group and no blinding as the objective was to assess the mass balance of masitinib after a single oral intake. There was only one group of healthy male volunteers. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05200169
Study type Interventional
Source AB Science
Contact
Status Completed
Phase Early Phase 1
Start date July 31, 2017
Completion date September 1, 2017

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