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Comparison · NCT03007394-sae

Lorcaserin vs Placebo Oral Capsule: serious adverse events

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. Lorcaserin vs Placebo Oral Capsule: serious adverse events. Trial comparisons, record NCT03007394-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03007394-sae

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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 10.03390.01330.0839wilson
Risk in group 20.04840.02240.102wilson
Risk difference, group 1 minus group 2-0.0145-0.07150.0419newcombe hybrid score
Risk ratio, group 1 over group 20.7010.2032.42log
Odds ratio, group 1 over group 20.690.192.51log
Number needed to treat, for one fewer participant with a serious adverse event on Lorcaserin than on Placebo Oral Capsule69from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Lorcaserin10 mg capsule by mouth, twice a day, for 13 weeks~Lorcaserin: Lorcaserin Capsule4118EG000
Group 2Placebo Oral Capsule10 mg placebo capsule, twice a day, for 13 weeks~Placebo Oral Capsule: sugar pill to mimic lorcaserin 10mg capsule6124EG001

Harm

What it counts
Total, serious adverse events
Time frame
Adverse event data were collected every week during treatment and through study follow-up, a 13-week treatment phase with a 4-week follow-up period.

Source ClinicalTrials.gov

Trial

Title
Lorcaserin in the Treatment of Cocaine Use Disorder
NCT number
NCT03007394
Phases
PHASE2
Conditions
Cocaine-Related Disorders
Interventions
Lorcaserin, Placebo Oral Capsule
Lead sponsor
National Institute on Drug Abuse (NIDA)
Results first posted
2020-06-19

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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