Comparison · NCT02888080-sae
ACZ885 300 mg 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. ACZ885 300 mg vs Placebo: serious adverse events. Trial comparisons, record NCT02888080-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02888080-sae
On this page
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 | 0.15 | 0.0524 | 0.36 | wilson | |
| Risk in group 2 | 0.2 | 0.0807 | 0.416 | wilson | |
| Risk difference, group 1 minus group 2 | -0.05 | -0.287 | 0.192 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.75 | 0.192 | 2.93 | log | |
| Odds ratio, group 1 over group 2 | 0.706 | 0.136 | 3.66 | log | |
| Number needed to treat, for one fewer participant with a serious adverse event on ACZ885 300 mg than on Placebo | 20 | 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 | ACZ885 300 mg | ACZ885 300 mg | 3 | 20 | EG000 |
| Group 2 | Placebo | Placebo (s.c. once monthly for 6 months) | 4 | 20 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- 40 months
Source ClinicalTrials.gov
Trial
- Title
- Study of Efficacy, Safety and Tolerability of ACZ885 (Canakinumab) in Patients With Pulmonary Sarcoidosis
- NCT number
- NCT02888080
- Phases
- PHASE2
- Conditions
- Pulmonary Sarcoidosis
- Interventions
- ACZ885, Placebo
- Lead sponsor
- Novartis Pharmaceuticals
- Results first posted
- 2020-03-16
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT02888080?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
Read this comparison from software.
The record is JSON. No key.
GET https://conductscience.org/api/comparisons/v1/NCT02888080-sae