Found 24 matching trials
Study of PF614 Compared to OxyContin® in Healthy Volunteers (PF614-101) PHASE1 PF614 is an oxycodone prodrug that is designed for extended-release of oxyc...
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PRA Health Sciences - Early Development Services
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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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A Research Study of an Investigational Drug ALO-02 (Oxycodone Hydrochloride and Naltrexone Hydrochloride) in Patients With Moderate to Severe Chronic Low Back Pain PHASE3 The primary objective of the study is to determine the analgesic efficacy a...
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Coastal Clinical Research, Inc.
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A Study to Characterize the Abuse Liability of ALO-02 in Healthy, Non-Dependent, Recreational Opioid Users When ALO-02 Capsules Are Crushed and Snorted 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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Dose Proportionality Study Of PF-00345439 Formulation Under Fed Conditions PHASE1 To evaluate the dose proportionality of 5 mg, 20 mg and 40 mg of PF 0034543...
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Pfizer Investigational Site
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Single Dose Study, Pharmacokinetics of Oxycodone and PF614 Co-Administered With Nafamostat (PF614-MPAR-102) PHASE1 A single dose dose study to assess the pharmacokinetics (PK) of oxycodone, ...
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Quotient Sciences
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Pharmacokinetics Study of ALO-02 and OxyContin PHASE1 To characterize the single- and multiple-dose pharmacokinetics of oxycodone...
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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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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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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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