Comparison · NCT00087022-sae
Intervention 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. Intervention vs Placebo: serious adverse events. Trial comparisons, record NCT00087022-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00087022-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 | 0.0835 | 0.0609 | 0.113 | wilson | |
| Risk in group 2 | 0.0849 | 0.062 | 0.115 | wilson | |
| Risk difference, group 1 minus group 2 | -0.00138 | -0.0393 | 0.0363 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.984 | 0.632 | 1.53 | log | |
| Odds ratio, group 1 over group 2 | 0.982 | 0.606 | 1.59 | log | |
| Number needed to treat, for one fewer participant with a serious adverse event on Intervention than on Placebo | 725 | 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 | Intervention | Patients receive monoclonal chimeric antibody cG250 (WX-G250) IV over 15 minutes as a single loading dose of 50 mg (week 1) followed by weekly infusions of 20 mg of WX-G250 (weeks 2-24).~girentuximab: Given IV | 36 | 431 | EG000 |
| Group 2 | Placebo | Patients receive placebo IV over 15 minutes once weekly for 24 weeks.~placebo: Given IV | 36 | 424 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
Source ClinicalTrials.gov
Trial
- Title
- Monoclonal Antibody Therapy (Rencarex®) in Treating Patients Who Have Undergone Surgery for Non-metastatic Kidney Cancer
- NCT number
- NCT00087022
- Phases
- PHASE3
- Conditions
- Kidney Cancer
- Interventions
- girentuximab, placebo
- Lead sponsor
- Heidelberg Pharma AG
- Results first posted
- 2018-09-12
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00087022?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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