Comparison · NCT00456521-sae
NB32 vs Placebo: serious adverse events
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
Cite this record
ConductScience Library. NB32 vs Placebo: serious adverse events. Trial comparisons, record NCT00456521-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00456521-sae
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Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.0377 | 0.025 | 0.0564 | wilson | |
| Risk in group 2 | 0.005 | 0.000883 | 0.0278 | wilson | |
| Risk difference, group 1 minus group 2 | 0.0327 | 0.00661 | 0.0518 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 7.53 | 1.02 | 55.5 | log | |
| Odds ratio, group 1 over group 2 | 7.79 | 1.04 | 58.2 | log | |
| Number needed to harm, for one more participant with a serious adverse event on NB32 than on Placebo | 30.6 | 19.3 | 151 | from the risk difference interval |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: placebo.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | NB32 | Naltrexone SR 32 mg/ bupropion SR 360 mg/ day | 22 | 584 | EG000 |
| Group 2 | Placebo | Placebo | 1 | 200 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- Baseline, 56 weeks
Source ClinicalTrials.gov
Trial
- Title
- A Safety and Efficacy Study of Naltrexone SR/Bupropion SR and Placebo in Overweight and Obese Subjects Participating in an Intensive Behavior Modification Program
- NCT number
- NCT00456521
- Phases
- PHASE3
- Conditions
- Obesity, Overweight
- Interventions
- Naltrexone SR 32 mg/ bupropion SR 360 mg/ day, Placebo, Intensive group lifestyle modification counseling
- Lead sponsor
- Orexigen Therapeutics, Inc
- Results first posted
- 2014-11-21
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00456521?tab=results
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.
For software
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GET https://conductscience.org/api/comparisons/v1/NCT00456521-sae