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Clinical Trial Summary

The purpose of this study is to examine the abuse potential and pharmacokinetics of PF614 compared with a non-abuse deterrent, commercially available, immediate release (IR) oxycodone hydrochloride (HCl) formulation and placebo.


Clinical Trial Description

This will be a randomized, double-blind, placebo-and active-controlled, 3-way crossover study to evaluate the abuse potential and pharmacokinetics of intranasally administered PF614, relative to crushed oxycodone HCl IR tablets and placebo in non-dependent recreational opioid users. The study will consist of 4 phases: Screening, Qualification, Treatment, and Follow-up. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05567354
Study type Interventional
Source Ensysce Biosciences
Contact
Status Completed
Phase Phase 1
Start date June 10, 2022
Completion date August 31, 2022

See also
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Completed NCT05571345 - A Study to Evaluate the Oral Abuse Potential of PF614 in Non-Dependent Recreational Opioid Users Phase 1
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