Comparison · NCT02495844-080dd0c8
UCB0942/UCB0942 (SS) vs Placebo/UCB0942 (SS): Number of Subject Withdrawals Due to Adverse Events (AEs) During the Course of the Study
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. UCB0942/UCB0942 (SS) vs Placebo/UCB0942 (SS): Number of Subject Withdrawals Due to Adverse Events (AEs) During the Course of the Study. Trial comparisons, record NCT02495844-080dd0c8. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02495844-080dd0c8
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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 | 0.0357 | 0.00633 | 0.177 | wilson | |
| Risk in group 2 | 0 | 0 | 0.125 | wilson | |
| Risk difference, group 1 minus group 2 | 0.0357 | -0.0923 | 0.177 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | log | a group has no participants with the outcome | |||
| Odds ratio, group 1 over group 2 | log | a cell of the two-by-two table is zero | |||
| Number needed to treat, for one more participant with the outcome on UCB0942/UCB0942 (SS) than on Placebo/UCB0942 (SS) | 28 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: placebo.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | UCB0942/UCB0942 (SS) | Subjects received UCB0942. | 1 | 28 | OG001 |
| Group 2 | Placebo/UCB0942 (SS) | After 2-week in the Inpatient Period, Placebo subjects received the experimental medicine (UCB0942). | 0 | 27 | OG000 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Number of Subject Withdrawals Due to Adverse Events (AEs) During the Course of the Study
- Description
- Number of subjects who withdrew from the study due adverse event (reported by the subject and/or caregiver or observed by the Investigator or inpatient staff).
- Time frame
- All study duration (approximately 19 to 20 weeks)
- Population
Source ClinicalTrials.gov
Trial
- Title
- A Study of UCB0942 in Adult Patients With Highly Drug-resistant Focal Epilepsy
- NCT number
- NCT02495844
- Phases
- PHASE2
- Conditions
- Highly Drug-resistant Focal Epilepsy
- Interventions
- UCB0942, UCB0942, Placebo
- Lead sponsor
- UCB Biopharma S.P.R.L.
- Results first posted
- 2019-02-05
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT02495844?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.
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