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Comparison · NCT02930018-sae

Nerinetide, 2.6 mg/kg 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

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ConductScience Library. Nerinetide, 2.6 mg/kg vs Placebo: serious adverse events. Trial comparisons, record NCT02930018-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02930018-sae

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.3310.2930.371wilson
Risk in group 20.3570.3190.398wilson
Risk difference, group 1 minus group 2-0.0265-0.08230.0296newcombe hybrid score
Risk ratio, group 1 over group 20.9260.7861.09log
Odds ratio, group 1 over group 20.8890.6931.14log
Number needed to treat, for one fewer participant with a serious adverse event on Nerinetide, 2.6 mg/kg than on Placebo37.7from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Nerinetide, 2.6 mg/kgSingle intravenous infusion of nerinetide over 10 ± 1 minutes181547EG001
Group 2PlaceboDrug vehicle only~Placebo: Placebo Comparator: Placebo198554EG000

Harm

What it counts
Total, serious adverse events
Time frame
Adverse Events occurring within 30 days of randomization and all Serious Adverse Events up to the end of study visit (Day 90 visit or death) or until the subject was deemed lost to follow-up were reported.

Source ClinicalTrials.gov

Trial

Title
Safety and Efficacy of Nerinetide (NA-1) in Subjects Undergoing Endovascular Thrombectomy for Stroke
NCT number
NCT02930018
Phases
PHASE3
Conditions
Stroke, Acute
Interventions
Nerinetide (NA-1), 2.6 mg/kg, Placebo
Lead sponsor
NoNO Inc.
Results first posted
2020-12-14

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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