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Comparison · NCT01704196-eecb841f

Nepicastat vs Placebo: Abstinence (Weeks 10 - 11)

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Nepicastat vs Placebo: Abstinence (Weeks 10 - 11). Trial comparisons, record NCT01704196-eecb841f. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01704196-eecb841f

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.04440.01740.109wilson
Risk in group 20.07870.03860.154wilson
Risk difference, group 1 minus group 2-0.0342-0.1140.0416newcombe hybrid score
Risk ratio, group 1 over group 20.5650.1711.86log
Odds ratio, group 1 over group 20.5450.1541.93log
Number needed to treat, for one fewer participant with the outcome on Nepicastat than on Placebo29.2from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Nepicastat
Nepicastat 120mg and 100mg riboflavin (once per day) for 11 weeks~Nepicastat: 120 mg of active drug and 100mg of riboflavin daily for 11 weeks or matching placebo containing 100mg of riboflavin daily for 11 weeks.
490OG000
Group 2PlaceboPlacebo capsule containing 100mg riboflavin (once per day) for 11 weeks.~Placebo789OG001

Outcome

Type
PRIMARY
Title
Abstinence (Weeks 10 - 11)
Description
Number of subjects that abstained from cocaine from weeks 10 through 11
Time frame
Weeks 10 - 11
Population

Source ClinicalTrials.gov

Trial

Title
A Multi-Center Trial of Nepicastat for Cocaine Dependence
NCT number
NCT01704196
Phases
PHASE2
Conditions
Cocaine Dependence
Interventions
Nepicastat, Placebo
Lead sponsor
National Institute on Drug Abuse (NIDA)
Results first posted
2017-05-18

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
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

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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