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A Randomized, Two-way, Crossover Study to Estimate the Relative Bioavailability of a Controlled-release Formulation of Oxycodone (40 mg) With Sequestered Naltrexone Compared With Immediate-release Oxycodone Tablets (20 mg) in Healthy Volunteers N/A To determine whether the bioavailability of the controlled-release test for...
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Pfizer Investigational Site
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Evaluation of Oral PF614 Relative to OxyContin (PF614-102) PHASE1 This is a single-center study incorporating 2 parts: A Multiple Ascending D...
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PRA Health Sciences-Early Development Services
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Safety and Pharmacokinetic Study of ALO-02 in Children Ages 7-17 With Pain PHASE4 Safety and pharmacokinetics of an abuse-deterrent, extended-release formula...
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Research Center For Clinical Studies-West, Inc.
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Study to Determine the Effects of Co-Administration of Alcohol on the Absorption of Oxycodone From a Proprietary Controlled-Release Formulation PHASE1 The study is designed to test whether or not the rate and extent of absorpt...
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Pfizer Investigational Site
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Pharmacokinetics of Oxycodone and PF614 Co-Administered with Nafamostat (PF614-MPAR-101) PHASE1 A single dose study to assess the pharmacokinetics (PK) of oxycodone, when ...
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Quotient Sciences
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Pharmacokinetics And Relative Bioavailability Study Of Oxycodone in Healthy Volunteers PHASE1 To estimate the pharmacokinetics and relative bioavailability of oxycodone ...
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Pfizer Investigational Site
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Single-Dose, Crossover Study To Compare Bioavailability Of Two Formulations Under Fed And Fasted Conditions PHASE1 To Compare The Bioavailability Of 40 Mg Doses Of Pf-00345439 Modified Formu...
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Pfizer Investigational Site
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Healthy Volunteers Study to Estimate the Effects of Food on the Bioavailability of Oxycodone and Naltrexone/6- ฮ -Naltrexol From a Extended Release Formulation of Oxycodone With Sequestered Naltrexone PHASE1 The purpose of this study is to estimate the effects of food and of sprinkl...
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Pfizer Investigational Site
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Study to Evaluate the Subjective Effects of PTI-801 in Non-Physically Dependent Subjects With a History of Drug Abuse PHASE2 This is a single-center, randomized, 7-way crossover, double-blind, active ...
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Behavioral Pharmacology Research Unit
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A Study to Characterize the Abuse Liability of ALO-02 in Healthy, Non-Dependent, Recreational Opioid Abusers PHASE1 The main purpose of this study is to determine if oxycodone and naltrexone ...
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INC Research Toronto, Inc.
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