Comparison · NCT03150875-sae
Sintilimab vs Docetaxel: 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. Sintilimab vs Docetaxel: serious adverse events. Trial comparisons, record NCT03150875-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03150875-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 | 0.389 | 0.313 | 0.47 | wilson | |
| Risk in group 2 | 0.262 | 0.194 | 0.343 | wilson | |
| Risk difference, group 1 minus group 2 | 0.127 | 0.016 | 0.233 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.49 | 1.04 | 2.12 | log | |
| Odds ratio, group 1 over group 2 | 1.8 | 1.07 | 3.01 | log | |
| Number needed to harm, for one more participant with a serious adverse event on Sintilimab than on Docetaxel | 7.85 | 4.28 | 62.5 | 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 | Sintilimab | Sintilimab 200mg Intravenously every 3 weeks | 56 | 144 | EG000 |
| Group 2 | Docetaxel | Docetaxel 75mg/m2 Intravenously every 3 weeks | 34 | 130 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- Through database cutoff date of 31-July-2020 (up to approximately 35 months)
Source ClinicalTrials.gov
Trial
- Title
- A Study Comparing the Efficacy and Safety Between IBI308 and Docetaxel in Patients With Advanced or Metastatic NSCLC
- NCT number
- NCT03150875
- Phases
- PHASE3
- Conditions
- Non-small Cell Lung Cancer
- Interventions
- IBI308, Docetaxel
- Lead sponsor
- Innovent Biologics (Suzhou) Co. Ltd.
- Results first posted
- 2021-06-23
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT03150875?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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GET https://conductscience.org/api/comparisons/v1/NCT03150875-sae