Comparison · NCT03572933-sae
Ganaxolone 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. Ganaxolone vs Placebo: serious adverse events. Trial comparisons, record NCT03572933-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03572933-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 | 0.12 | 0.0562 | 0.238 | wilson | |
| Risk in group 2 | 0.098 | 0.0426 | 0.21 | wilson | |
| Risk difference, group 1 minus group 2 | 0.022 | -0.107 | 0.152 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.22 | 0.399 | 3.75 | log | |
| Odds ratio, group 1 over group 2 | 1.25 | 0.357 | 4.41 | log | |
| Number needed to harm, for one more participant with a serious adverse event on Ganaxolone than on Placebo | 45.5 | 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 | Ganaxolone | ganaxolone suspension (50 mg/ml) 3x's /day for 17 weeks~ganaxolone: active drug | 6 | 50 | EG001 |
| Group 2 | Placebo | placebo suspension 3x's /day for 17 weeks~Placebo: inactive | 5 | 51 | EG000 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- Screening through 17-week Double-blind Phase
Source ClinicalTrials.gov
Trial
- Title
- Study of Adjunctive Ganaxolone Treatment in Children and Young Adults With CDKL5 Deficiency Disorder
- NCT number
- NCT03572933
- Phases
- PHASE3
- Conditions
- CDKL5 Deficiency Disorder
- Interventions
- ganaxolone, Placebo
- Lead sponsor
- Marinus Pharmaceuticals
- Results first posted
- 2022-07-26
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT03572933?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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