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Comparison · NCT02930018-e12ca8eb

Nerinetide, 2.6 mg/kg vs Placebo: Number of Subjects With mRS Score of 0 to 2

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: Number of Subjects With mRS Score of 0 to 2. Trial comparisons, record NCT02930018-e12ca8eb. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02930018-e12ca8eb

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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 10.6140.5720.654wilson
Risk in group 20.5920.550.632wilson
Risk difference, group 1 minus group 20.0221-0.03550.0795newcombe hybrid score
Risk ratio, group 1 over group 21.040.9431.14log
Odds ratio, group 1 over group 21.10.8621.4log
Number needed to treat, for one more participant with the outcome on Nerinetide, 2.6 mg/kg than on Placebo45.2from 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 minutes337549OG001
Group 2PlaceboDrug vehicle only~Placebo: Placebo Comparator: Placebo329556OG000

Outcome

Type
PRIMARY
Title
Number of Subjects With mRS Score of 0 to 2
Description
Overall number of subjects experiencing a favorable functional outcome 90 days post-randomization, defined as 0 to 2 on the mRS.~The modified Rankin Scale (mRS) is a valid and reliable clinician-reported measure of global disability that has been widely applied for evaluating recovery from stroke. It is a scale used to measure functional recovery (the degree of disability or dependence in daily activities) of people who have suffered a stroke. mRS scores range from 0 (best outcome) to 6 (worst outcome), with 0 indicating no residual symptoms; 5 indicating bedbound, requiring constant care; and 6 indicating death.
Time frame
90 Days
Population
Intent-to-Treat Population

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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