Comparison · NCT05678959-sae
Ligelizumab 120 mg vs Ligelizumab 240 mg: 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. Ligelizumab 120 mg vs Ligelizumab 240 mg: serious adverse events. Trial comparisons, record NCT05678959-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT05678959-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 | 0.037 | 0.0127 | 0.103 | wilson | |
| Risk in group 2 | 0.0244 | 0.00671 | 0.0846 | wilson | |
| Risk difference, group 1 minus group 2 | 0.0126 | -0.0523 | 0.0812 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.52 | 0.261 | 8.85 | log | |
| Odds ratio, group 1 over group 2 | 1.54 | 0.25 | 9.46 | log | |
| Number needed to harm, for one more participant with a serious adverse event on Ligelizumab 120 mg than on Ligelizumab 240 mg | 79.1 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Ligelizumab 120 mg | Participants received ligelizumab 120 mg and matching placebo (to protect the dose blinding) every 4 weeks. | 3 | 81 | EG000 |
| Group 2 | Ligelizumab 240 mg | Participants received ligelizumab 240 mg every 4 weeks. | 2 | 82 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- Adverse events were reported from first dose of study treatment until end of study treatment plus 16 weeks post treatment, up to a maximum duration of approximately 81 weeks.
Source ClinicalTrials.gov
Trial
- Title
- Long-term Extension Study of Ligelizumab in Food Allergy
- NCT number
- NCT05678959
- Phases
- PHASE3
- Conditions
- Food Allergy
- Interventions
- Ligelizumab 120 mg, Ligelizumab 240 mg
- Lead sponsor
- Novartis Pharmaceuticals
- Results first posted
- 2025-10-30
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT05678959?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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