Comparison · NCT02324582-sae
Intravenous MK-3475-100 mg/ Intravesical BCG vs Intravenous MK-3475-200 mg/ Intravesical BCG: 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. Intravenous MK-3475-100 mg/ Intravesical BCG vs Intravenous MK-3475-200 mg/ Intravesical BCG: serious adverse events. Trial comparisons, record NCT02324582-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02324582-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 | 0.0000000000000000555 | 0.561 | wilson | |
| Risk in group 2 | 0.6 | 0.313 | 0.832 | wilson | |
| Risk difference, group 1 minus group 2 | -0.6 | -0.832 | 0.0307 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | log | a group has no participants with the outcome | |||
| Odds ratio, group 1 over group 2 | log | a cell of the two-by-two table is zero | |||
| Number needed to treat, for one fewer participant with a serious adverse event on Intravenous MK-3475-100 mg/ Intravesical BCG than on Intravenous MK-3475-200 mg/ Intravesical BCG | 1.67 | 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 | Intravenous MK-3475-100 mg/ Intravesical BCG | 3 subjects will be treated at a dose of 100 mg MK-3475 at 100 mg every 3 weeks (Q3W) intravenously (IV) for 6 doses and 1 vial (50mg) intravesicular BCG suspended in 50 ml preservative-free saline once per week of 6 weekly doses | 0 | 3 | EG000 |
| Group 2 | Intravenous MK-3475-200 mg/ Intravesical BCG | Up to 12 subjects will be treated at a dose of 200 mg MK-3475 at 100 mg every 3 weeks (Q3W) intravenously (IV) for 6 doses and 1 vial (50 mg) intravesicular BCG suspended in 50 ml preservative-free saline once per week of 6 weekly doses | 6 | 10 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
Each subject had adverse events collected from the time of consent through 30 days post-treatment completion with MK-3475/pembrolizumab. This was up to 23 weeks from the time of first treatment with MK-3475/pembrolizumab.
Source ClinicalTrials.gov
Trial
- Title
- MK-3475/BCG in High Risk Superficial Bladder Cancer
- NCT number
- NCT02324582
- Phases
- PHASE1
- Conditions
- Bladder Cancer
- Interventions
- Intravenous MK-3475/ Intravesical BCG
- Lead sponsor
- Southern Illinois University
- Results first posted
- 2024-09-03
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT02324582?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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