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Clinical Trial Summary

The primary objective of this trial is to assess the effect of probenecid on the pharmacokinetics (PK) of single-dose pexidartinib in healthy subjects.

Secondary objectives are to assess the safety and tolerability of pexidartinib alone and in combination with probenecid.

Participants will be confined to the clinic for approximately 32 days. Blood samples will be collected for PK analysis of pexidartinib and metabolites at predose and up to 312 hours (h) post dose.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Pharmacokinetics in Healthy Volunteers

NCT number NCT03138759
Study type Interventional
Source Daiichi Sankyo Inc.
Contact
Status Completed
Phase Phase 1
Start date February 27, 2017
Completion date March 30, 2017