Evidence map›Paper›PMID 41919765›Full record

Trial reportEpilepsia2026

Systematic statistical analysis of change in SEIzure interVAL with diazepam nasal spray supports this novel clinical endpoint for immediate-use seizure medication.

Wesley T Kerr, Katherine N McFarlane, Leock Y Ngo, Enrique Carrazana, Adrian L Rabinowicz

Registry-linked trialAbstract readClinical Trial, Phase III
In one paragraph

Trial report in Epilepsia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02721069 (A 12-Month Open-Label, Repeat-Dose Safety Study of NRL-1 in Epilepsy Subjects), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02721069 phase3completednot on this map

A 12-Month Open-Label, Repeat-Dose Safety Study of NRL-1 in Epilepsy Subjects (DIAZ.001.05)

TypeinterventionalSponsorNeurelis, Inc.Ran2016 to 2020Enrolled175ConditionsAcute Repetitive Seizures, Breakthrough SeizuresArmsNRL-1
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Trial
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Wesley T KerrDivision of Epilepsy, Department of Neurology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.ORCID https://orcid.org/0000-0002-5546-5951
Katherine N McFarlaneDivision of Epilepsy, Department of Neurology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.ORCID https://orcid.org/0009-0000-0365-813X
Leock Y NgoNeurelis, San Diego, California, USA.ORCID https://orcid.org/0000-0002-8184-1367
Enrique CarrazanaNeurelis, San Diego, California, USA.ORCID https://orcid.org/0000-0001-8788-0722
Adrian L RabinowiczNeurelis, San Diego, California, USA.ORCID https://orcid.org/0000-0003-1299-0606

Funding

Feasibility of machine learning to improve the diagnostic odyssey for functional seizuresK23NS135134 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Wesley Thomas Kim Kerr · 2025 to 2026
$448k
Neurelis, Inc. W.T.K's research time funded by the National Institute of Neurological Disorders and Stroke K23NS135134NINDS NIH HHS K23 NS135134
6 · The paper itself

Abstract

objectiveAppropriate endpoints for daily antiseizure medications may differ from those for intermittent, immediate-use seizure medications (ISMs). The observed interval between seizure clusters over time (SEIzure interVAL [SEIVAL]) has been proposed as a novel effectiveness endpoint for ISMs. SEIVAL was initially identified pragmatically. This post hoc analysis evaluated how the study timeline and participant characteristics could impact the measurement of SEIVAL using data from an open-label study of intermittent treatment with diazepam nasal spray.

methodsThis analysis includes data from a long-term, phase 3 safety study of diazepam nasal spray, which enrolled patients aged 6-65 years with epilepsy and seizure clusters (NCT02721069). Study timeline and participant characteristic choices were evaluated systematically to determine the impact on effect size, and thereby statistical power, using data regarding individual treated seizure clusters. In this strategy, the date of the first treated seizure cluster constituted day 1 of the baseline period; consecutive 70-day periods were used for analysis. The change in SEIVAL for each patient was calculated using each measured SEIVAL for that patient in the primary outcome period (days 71-140) minus that patient's mean SEIVAL in the baseline period (days 1-70) with mixed effects linear regression.

resultsMean SEIVAL increased from 13 days at baseline (days 1-70) to 24 days in the primary outcome period (days 71-140, p < .0001). SEIVAL lengthening was seen in adults, adolescents (ages 6-17 years), and children (ages 6-12 years), with further lengthening past 140 days in adolescents and children. SEIVAL lengthened more in participants with <1 SEIVAL per 2 weeks at baseline than higher SEIVAL frequency. SIGNIFICANCE: This systematically planned analysis expands on and reinforces the previous pragmatic analysis that introduced the SEIVAL metric. The present analysis provides a novel framework for future studies of intermittently administered ISMs to treat seizure clusters such as diazepam nasal spray.

Indexed as

AnticonvulsantsDiazepamEpilepsySeizuresAdministration, IntranasalAdolescentAdultAgedChildFemaleHumansMaleMiddle AgedNasal SpraysTime FactorsTreatment OutcomeAnticonvulsantsDiazepamNasal Spraysbenzodiazepineepilepsyintranasalrescueseizure cluster

Identifiers

PMID41919765
PMCPMC13361021

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.