Mode
Text Size
Log in / Sign up
Early Phase 1 N=19 Randomized Quadruple-blind Health Services Research

Pilot Study of Entacapone for Methamphetamine Abuse

Methamphetamine Dependence

Enrolled (actual)
19
Serious AEs
0.0%
Results posted
Sep 2019
Primary outcome: Primary: Effect of Entacapone on Methamphetamine-induced Mood — 12.500; 13.750; 7.500; 9.833 units on a scale

Study Design & Population

Study type
Interventional
Phase
Early Phase 1
Interventions
Entacapone (Drug); Methamphetamine (Drug); Placebo (Drug)
Age
Adult · 18+ yrs
Sex
All
Sponsor
Oregon Health and Science University
Primary completion
Jun 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Effect of Entacapone on Methamphetamine-induced Mood
12.500; 13.750; 7.500; 9.833; 8.750
PRIMARY
Effect of Entacapone on Subjective Effects of Methamphetamine
1.9375; 1.8333; 7.9167; 2.5833; 6.9167; 3.0625
PRIMARY
Effect of Entacapone on Methamphetamine-induced Stimulation
0.1667; 0.1667; 1.4167; 0.4167; 1.3333
SECONDARY
Cognitive Function
38.813; 40.500; 41.333; 42.583; 40.083; 73.167

Summary

Addiction to methamphetamine is a serious health problem. There are no medications that a doctor can give someone to help them stop using methamphetamine. Entacapone (Comtan©) is a medication that could help people addicted to methamphetamine. This study will see how entacapone works in healthy people who are given methamphetamine. We think that the study drug will be well tolerated, and that it will prevent some of the effects of methamphetamine that make it so addictive. We also want to see how differences in people's genes may cause differences in the ways the study drug and methamphetamine work for them. The study has six total visits. The first visit is for screening. Tests and procedures will make sure it is safe for subjects to participate. The second visit is a familiarization day. Subjects will receive methamphetamine, but no entacapone. This is done to make sure they can tolerate the drug and recognize its effects before being given a second drug on the same day. Subjects will take surveys and computer tests to see how the medications change mood, thinking, and liking the drug. The final four visits are the actual study days. Subjects will be randomly assigned (like the flip of a coin) to the different ways to get either 1) study medication or placebo (placebo contains no active study medication) and then 2) methamphetamine or placebo. Subjects will be in all four groups during the study, which means that each day a subject will get a different group.

Eligibility Criteria

Inclusion Criteria

  • No history of pre-existing physical (including cardiovascular) illness
  • No history of drug abuse or dependence
  • Ability to read and write English
  • Have had at least one exposure to a stimulant (e.g. cocaine, methamphetamine, ecstasy, methylphenidate or any medication in the stimulant class) in their lifetime

Exclusion Criteria

  • Pregnant
  • Taking any psychotropic medication
  • Meeting DSM-IV criteria for active substance abuse or dependence
  • On any stimulant medication
  • History or current hypertension (BP > 140/90 mm Hg) or systolic hypotension (SBP 90/min
  • Any active medical illness
  • Family history of abnormal heart rhythms, or sudden cardiac death
  • Subjects who anticipate they may require the emergent use of epinephrine (such as an Epi-Pen®) for the treatment of severe allergic reactions
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02058966). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search