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Trial · NCT03539432

Exploration of Gemfibrozil as a Treatment for AUD

NCT03539432, Phase 2, Terminated, The Mind Research Network; results first posted 2021-10-18

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Exploration of Gemfibrozil as a Treatment for AUD. Trials, record NCT03539432. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03539432

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Exploration of Gemfibrozil as a Treatment for AUD
NCT number
NCT03539432
Status
Terminated
Phases
Phase 2
Enrollment
3 participants, actual
Lead sponsor
The Mind Research Network
Conditions
Alcohol Use Disorder
Interventions
Gemfibrozil 600 MG, Placebo oral capsule
First posted
2018-05-29
Last updated
2021-10-29
Results first posted
2021-10-18

Source ClinicalTrials.gov

Registered outcomes6

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryMean Standard Drinks Per Drinking DayBaselineAverage number of standard drinks consumed on drinking days
PrimaryMean Standard Drinks Per Drinking Day2 weeks post baselineAverage number of standard drinks consumed on drinking days
PrimaryMean Standard Drinks Per Drinking Day4 weeks post baselineAverage number of standard drinks consumed on drinking days
PrimaryPercent Days AbstinentBaselinePercentage of days of abstinence from alcohol
PrimaryPercent Days Abstinent2 weeks post baselinePercentage of days of abstinence from alcohol
PrimaryPercent Days Abstinent4 weeks post baselinePercentage of days of abstinence from alcohol

Outcomes6

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYMean Standard Drinks Per Drinking DayBaselineDrinks per drinking dayMEAN
PRIMARYMean Standard Drinks Per Drinking Day2 weeks post baselineThe one participant in the placebo condition dropped out before taking any medicationDrinks per drinking dayMEAN
PRIMARYMean Standard Drinks Per Drinking Day4 weeks post baselineThe one participant in the placebo condition dropped out before taking any medicationDrinks per drinking dayMEAN
PRIMARYPercent Days AbstinentBaselinePercentage of abstinent daysMEAN
PRIMARYPercent Days Abstinent2 weeks post baselineThe one participant in the placebo condition dropped out before taking any medicationPercentage of abstinent daysMEAN
PRIMARYPercent Days Abstinent4 weeks post baselineThe one participant in the placebo condition dropped out before taking any medicationPercentage of abstinent daysMEAN

Results by group8

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Mean Standard Drinks Per Drinking DayGemfibrozil6.17Full Range 5.57 to 6.76Drinks per drinking day
Mean Standard Drinks Per Drinking DayPlacebo8.59Full Range 8.59 to 8.59Drinks per drinking day
Mean Standard Drinks Per Drinking DayGemfibrozil4.12Full Range 3.58 to 4.667Drinks per drinking day
Mean Standard Drinks Per Drinking DayGemfibrozil2.18Full Range 2 to 2.35Drinks per drinking day
Percent Days AbstinentGemfibrozil31Full Range 16.7 to 44.4Percentage of abstinent days
Percent Days AbstinentPlacebo32.2Full Range 32.2 to 32.2Percentage of abstinent days
Percent Days AbstinentGemfibrozil45.5Full Range 0 to 90.9Percentage of abstinent days
Percent Days AbstinentGemfibrozil45Full Range 0 to 90Percentage of abstinent days

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDGemfibrozil2
Overall StudySTARTEDPlacebo1
Overall StudyCOMPLETEDGemfibrozil2
Overall StudyCOMPLETEDPlacebo0
Overall StudyNOT COMPLETEDGemfibrozil0
Overall StudyNOT COMPLETEDPlacebo1

Adverse events6

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAbdominal painGastrointestinal disordersGemfibrozil121
otherAbdominal painGastrointestinal disordersPlacebo010
otherFatigueNervous system disordersGemfibrozil121
otherFatigueNervous system disordersPlacebo010
otherBruisingSkin and subcutaneous tissue disordersGemfibrozil121
otherBruisingSkin and subcutaneous tissue disordersPlacebo010

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityGemfibrozil02
Total, all-cause mortalityPlacebo01
Total, other adverse eventsGemfibrozil12
Total, other adverse eventsPlacebo01
Total, serious adverse eventsGemfibrozil02
Total, serious adverse eventsPlacebo01

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons2

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource
Gemfibrozil vs Placebo: deaths from any causeTrial comparisons
Gemfibrozil vs Placebo: serious adverse eventsTrial comparisons

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT03539432

GET https://conductscience.org/api/trials/v1/NCT03539432/registered