Comparison · NCT04462536-c5ec02eb
Nerinetide vs Placebo: Mortality Rate, as Defined by Event Rate (Percent) for Mortality Over the 90-day Study Period.
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
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ConductScience Library. Nerinetide vs Placebo: Mortality Rate, as Defined by Event Rate (Percent) for Mortality Over the 90-day Study Period. Trial comparisons, record NCT04462536-c5ec02eb. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04462536-c5ec02eb
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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 | 0.192 | 0.158 | 0.23 | wilson | |
| Risk in group 2 | 0.177 | 0.142 | 0.217 | wilson | |
| Risk difference, group 1 minus group 2 | 0.0149 | -0.0378 | 0.0667 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.08 | 0.816 | 1.44 | log | |
| Odds ratio, group 1 over group 2 | 1.1 | 0.779 | 1.56 | log | |
| Number needed to treat, for one more participant with the outcome on Nerinetide than on Placebo | 67.3 | 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 | Nerinetide | Single intravenous infusion of nerinetide 2.6 mg/kg (up to a maximum dose of 270 mg) over 10 ± 1 minutes~Nerinetide: Single intravenous infusion of nerinetide 2.6 mg/kg (up to a maximum dose of 270 mg) over 10 ± 1 minutes | 87 | 454 | OG001 |
| Group 2 | Placebo | Vehicle only~Placebo: Vehicle only | 70 | 396 | OG000 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Mortality Rate, as Defined by Event Rate (Percent) for Mortality Over the 90-day Study Period.
- Description
The estimand of mortality rate was the adjusted unconditional population difference in the number of deaths observed divided by the number of participants observed over the 90-day study period (mortality proportions) between treatment conditions (nerinetide vs. placebo) in the target patient population at Day 90. Deaths occurring over the Day 90 period were considered as non-responses.
- Time frame
- 90 days
- Population
- ITT Population
Source ClinicalTrials.gov
Trial
- Title
- Efficacy and Safety of Nerinetide in Participants With Acute Ischemic Stroke Undergoing Endovascular Thrombectomy Excluding Thrombolysis
- NCT number
- NCT04462536
- Phases
- PHASE3
- Conditions
- Stroke, Acute
- Interventions
- Placebo, Nerinetide
- Lead sponsor
- NoNO Inc.
- Results first posted
- 2025-06-22
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT04462536?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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