Safety, Pharmacokinetics, Bioavailability, Food Effect, Drug-Drug

Clinical Trial Summary

This is a Phase l double-blind, placebo-controlled, randomized study to investigate the safety, tolerability, pharmacokinetics, bioavailability and food effect of single doses of APX001 administered intravenously and orally, followed by an evaluation of the safety, tolerability, pharmacokinetics and drug-drug interaction potential of multiple doses of APX001 administered orally.

See also
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NCT number	NCT02957929
Study type	Interventional
Source	Pfizer
Contact
Status	Completed
Phase	Phase 1
Start date	October 31, 2016
Completion date	April 20, 2017

Safety, Pharmacokinetics, Bioavailability, Food Effect, Drug-Drug Interaction Study of APX001 Administered Orally

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms