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Bioavailability, Safety and Tolerability of Diazepam Nasal Spray Versus Diazepam Rectal Gel (Diastat®)

Phase 2
Terminated
Conditions
Refractory Epilepsy
Interventions
Registration Number
NCT02474407
Lead Sponsor
Acorda Therapeutics
Brief Summary

This is a multi-center, open-label, crossover, pharmacokinetic, bio-availability study involving adolescents and adults with refractory (drug-resistant) epilepsy. Cohort 1 comprises the subjects used to determine the relative bioavailability of DZNS versus DRG (Diastat)

Detailed Description

To determine the bioavailability of diazepam nasal spray versus diazepam rectal gel (Diastat®) under conditions of use in adolescent and adult persons with epilepsy (PWE) meeting the definition of refractory epilepsy.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
78
Inclusion Criteria
  • Diagnosis of refractory epilepsy
  • Body weight 26 to 111 kilogram (kg) inclusive
  • Other inclusion criteria apply
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Exclusion Criteria
  • Male or female subject who is not surgically sterile or female subject who is less than 2 years postmenopausal, and does not agree to use a highly effective birth control method during the study and up to 3 months after the last dose of investigational product
  • Female subject who is pregnant, breastfeeding, or planning to become pregnant
  • Presence or history of any abnormality or illness that may affect the absorption, distribution, metabolism or elimination of diazepam
  • Other exclusion criteria apply
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Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
diazepam rectal gel (DRG)diazepam rectal gelA single rectal dose of diazepam will be administered to subjects according to the Diastat prescribing information.
diazepam nasal spray (DZNS)diazepam nasal sprayOne dose of diazepam nasal spray is administered as two intranasal sprays; one in each nostril using a nasal spray device.
Primary Outcome Measures
NameTimeMethod
AUC 0-24h24 hours

Relative bioavailability based on area under time plasma concentration curve.

Cmax24 hours

Relative bioavailability based on maximum observed plasma concentration.

Secondary Outcome Measures
NameTimeMethod
Focused Nasal Exam (Part B)pre-dose (day 1) up to 24 hours post-dose

A focused nasal exam was completed by the Investigator in the treatment period(s) when diazepam nasal spray was administered, based on a visual inspection of the nasal mucosa. Focused Nasal Examination Part B - will show nasal mucosal symptoms that will be rated for severity will include discharge, mucosal edema, crusting, erythema, and epistaxis. This exam may be conducted within a 5 minute window after the specified time point. Between the 12 and 24 h time points, the exam was should be repeated every 4 hours as needed to follow any residual symptoms to resolution and the time of resolution should be documented.

(Categories with no data were omitted)

Focused Nasal Exam (Part A)pre-dose (day 1) up to 24 hours post-dose

A focused nasal exam was completed by the Investigator in the treatment period(s) when diazepam nasal spray was administered, based on a visual inspection of the nasal mucosa. Nasal irritation will be graded "none" to Grade 4 "septal perforation." Grade 1a= focal irritation, Grade 1b= superficial mucosal erosion, Grade 2= moderate mucosal erosion, Grade 3= ulceration, Grade 4= septal perforation. This exam may be conducted within a 5 minute window after the specified time point. Between the 12 and 24 h time points, the exam should be repeated every 4 hours as needed to follow any residual symptoms to resolution and the time of resolution should be documented.

(Categories with no data were omitted)

Smell Identification Test (SIT)day 1 up to day 31

The SIT is a validated test of smell identification which scores patients into different levels of olfactory function normalized by age and gender, however it had not been validated for use in PWE. The Smell Identification Test (SIT) is a 40-item multiple-choice standardized test. The test can be self-administered and consists of four 10-page booklets with a different "scratch and sniff" strip on each page. A scratch with a pencil releases the scent from the strip, and the subject is then asked to match the scent to one of four choices on the page. An answer must be selected for each of the 40 items, even when the subject cannot detect a smell. The total score (i.e., number of correct answers, range: 0-40) can be compared against normative data collected from approximately 4000 normal individuals between ages 4 to 99 to determine the subject's percentile rank of olfactory dysfunction corrected for age and gender.

Taste Change QuestionnaireUp to 24 hours

Questionnaire given to safety population in Cohort 1 for reporting taste change during the study. If the subject spontaneously reports an experience of taste change associated with diazepam nasal spray dosing, it will be evaluated qualitatively by the research staff using a taste change questionnaire. The subject will be asked to describe the type, intensity, and duration of the change in taste at multiple scheduled time points after dosing. Between the 12 and 24 h time points, the questionnaire should be repeated every 4 hours as needed to follow any residual symptoms to resolution, and time of resolution should be documented.

Trial Locations

Locations (22)

Acorda Site #101

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Tampa, Florida, United States

Acorda Site #112

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Saint Louis, Missouri, United States

Acorda Site #121

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Hackensack, New Jersey, United States

Acorda Site #114

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Portland, Oregon, United States

Acorda Site #105

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Philadelphia, Pennsylvania, United States

Acorda Site #125

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Honolulu, Hawaii, United States

Acorda Site #116

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Philadelphia, Pennsylvania, United States

Acorda Site #122

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Dallas, Texas, United States

Acorda Site #115

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Little Rock, Arkansas, United States

Acorda Site #127

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Washington, District of Columbia, United States

Acorda Site #104

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Lexington, Kentucky, United States

Acorda Site #128

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Edison, New Jersey, United States

Acorda Site #123

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Amherst, New York, United States

Acorda Site #111

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Baltimore, Maryland, United States

Acorda Site #132

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Chapel Hill, North Carolina, United States

Acorda Site #102

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Bethesda, Maryland, United States

Acorda Site #117

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Jackson, Mississippi, United States

Acorda Site #110

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Ann Arbor, Michigan, United States

Acorda Site #119

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Rochester, New York, United States

Acorda Site #130

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Memphis, Tennessee, United States

Acorda Site #103

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Bellaire, Texas, United States

Acorda Site #108

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Houston, Texas, United States

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