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Effects of MNTX on CYP450 2D6 in Metabolizers of Dextromethorphan

Phase 1
Completed
Conditions
Healthy Adults
Interventions
Registration Number
NCT01367535
Lead Sponsor
Bausch Health Americas, Inc.
Brief Summary

This study is a single-center, randomized, open-label, active and placebo-controlled, parallel-group, conducted in healthy male volunteers who have been shown to be extensive metabolizers of dextromethorphan.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
54
Inclusion Criteria
  1. Healthy males between the ages of 18 and 55
  2. Non-Smokers
  3. Body weight range form 154-220 lbs
  4. No history of clinically significant metabolic disorders.
Exclusion Criteria
  1. Any history of low CYP450 2D6 activity
  2. History of alcohol abuse or recreational drugs
  3. History of any clinically significant disease or condition affecting a major organ system
  4. Donation or loss of blood, 60 days proceeding to screening visit.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Arm 4SC Placebo-
Arm 2IV Methylnaltrexone (MNTX)-
Arm 1SC Methylnaltrexone (MNTX)-
Arm 3Oral Paroxetine-
Primary Outcome Measures
NameTimeMethod
Plasma Concentration of MNTX4 months

The objective of this study is to assess the effect of SC or IV doses of MNTX on CYP450 2D6 activity.

Secondary Outcome Measures
NameTimeMethod
Plasma Concentration of Paroxetine4 months

The objective of this study is to assess the effect of SC or IV doses of MNTX on CYP450 2D6 activity.

Trial Locations

Locations (1)

Progenics Pharmaceuticals

🇺🇸

Tarrytown, New York, United States

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