Comparison · NCT03172624-sae
R/M Adenoid Cystic Carcinoma (ACC) vs R/M SGC of Any Histology, Except ACC (Non ACC): 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. R/M Adenoid Cystic Carcinoma (ACC) vs R/M SGC of Any Histology, Except ACC (Non ACC): serious adverse events. Trial comparisons, record NCT03172624-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03172624-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 | 0.563 | 0.393 | 0.718 | wilson | |
| Risk in group 2 | 0.281 | 0.156 | 0.454 | wilson | |
| Risk difference, group 1 minus group 2 | 0.281 | 0.0396 | 0.481 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 2 | 1.06 | 3.76 | log | |
| Odds ratio, group 1 over group 2 | 3.29 | 1.16 | 9.3 | log | |
| Number needed to harm, for one more participant with a serious adverse event on R/M Adenoid Cystic Carcinoma (ACC) than on R/M SGC of Any Histology, Except ACC (Non ACC) | 3.56 | 2.08 | 25.3 | from the risk difference interval |
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 | R/M Adenoid Cystic Carcinoma (ACC) | Enrolled patients will be treated with nivolumab 3 mg/kg every 2 weeks plus ipilimumab 1 mg/kg every 6 weeks (1 cycle= 6 weeks).~Nivolumab: nivolumab 3 mg/kg every 2 weeks~Ipilimumab: ipilimumab 1 mg/kg every 6 weeks (1 cycle= 6 weeks) | 18 | 32 | EG000 |
| Group 2 | R/M SGC of Any Histology, Except ACC (Non ACC) | Enrolled patients will be treated with nivolumab 3 mg/kg every 2 weeks plus ipilimumab 1 mg/kg every 6 weeks (1 cycle= 6 weeks).~Nivolumab: nivolumab 3 mg/kg every 2 weeks~Ipilimumab: ipilimumab 1 mg/kg every 6 weeks (1 cycle= 6 weeks) | 9 | 32 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- 2 years
Source ClinicalTrials.gov
Trial
- Title
- Study of Nivolumab Plus Ipilimumab in Patients With Salivary Gland Cancer
- NCT number
- NCT03172624
- Phases
- PHASE2
- Conditions
- Salivary Gland Cancer
- Interventions
- Nivolumab, Ipilimumab
- Lead sponsor
- Memorial Sloan Kettering Cancer Center
- Results first posted
- 2025-12-18
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT03172624?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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