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Pilot Study to Evaluate the Duration of Effects on Simulated Car Driving and Cognitive Performance After a Single Dose of JNJ-42847922, Zolpidem and Placebo in Healthy Participants

23 marca 2016 zaktualizowane przez: Janssen-Cilag International NV

A Double-blind, Randomized, Controlled, 3-way Crossover, Pilot Study to Evaluate the Duration of Effects on Simulated Car Driving and Cognitive Performance After a Single Dose of JNJ-42847922, Zolpidem and Placebo in Healthy Subjects

The purpose of the study is to evaluate the effects of JNJ-42847922, compared to zolpidem and placebo, on driving performance as assessed by the mean difference of standard deviation of lateral position (SDLP) after forced awakening using a validated driving simulator test at 2, 4, 6 and 8 hours post-evening dose.

Przegląd badań

Status

Zakończony

Warunki

Interwencja / Leczenie

Szczegółowy opis

This is a single center, double-blind (neither Investigator nor participant knows which treatment the participant receives), randomized (study drug assigned by chance), 3-way cross-over (the same medications provided to all participants but in different sequence), pilot study in healthy male and female participants. Participants will be randomly assigned to 1 of 6 treatment and planning sequences. The study will consist of 3 parts: Screening Phase (between 21 days and 1 day prior to the first dose administration), a 3-way crossover double-blind, single dose treatment Phase and follow-up Phase (7 to 10 days after last dose administration). The maximum study duration for each participant will not exceed 7 weeks. The double-blind crossover treatment phase will consist of 3 treatment periods separated by a washout period of at least 3 days between dosing. Participants will receive either Treatment A (2 capsules of 20 milligram [mg] JNJ-42847922), Treatment B (10 mg zolpidem and 1 placebo capsule) or Treatment C (2 placebo capsules) in each treatment period. Driving performance will be assessed primarily by the mean difference of standard deviation of lateral position (SDLP) from an on road driving test. Participants' safety will be monitored throughout the study.

Typ studiów

Interwencyjne

Zapisy (Rzeczywisty)

36

Faza

  • Faza 1

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

18 lat do 55 lat (Dorosły)

Akceptuje zdrowych ochotników

Tak

Płeć kwalifikująca się do nauki

Wszystko

Opis

Inclusion Criteria:

  • Body mass index (BMI) (weight [kg]/height^2[m^2]) between 18 and 30 kg/m^2 (inclusive)
  • Men who are sexually active with a woman of childbearing potential must agree to use a condom, and all men must not donate sperm during the study and for 3 months after receiving the last dose of study drug. In addition, for men who have not had a vasectomy, their female partners should also use an appropriate method of birth control for at least the same duration
  • A woman of childbearing potential must have a negative serum pregnancy test at screening and a negative urine pregnancy test pre-dose on Day 1 of each period
  • A woman must agree not to donate eggs (ova, oocytes) for the purposes of assisted reproduction during the study and for at least 3 months after receiving the last dose of study drug
  • Participant has a valid driving license for more than 3 years, has driven at least 5000 kilometer (km) in the past year and is driving a car regularly
  • Women of childbearing potential must practice a highly effective method of birth control consistent with local regulations regarding the use of birth control methods for participants participating in clinical studies (that is, one that results in a less than 1 percent per year failure rate when used consistently and correctly)

Exclusion Criteria:

  • Participant has clinically significant liver or renal insufficiency; cardiac, vascular, pulmonary, gastrointestinal, endocrine, neurologic (including cataplexy and cognitive impairment), hematologic, rheumatologic, psychiatric, or metabolic disturbances. A significant primary sleep disorder is exclusionary
  • Clinically significant abnormal values for hematology, clinical chemistry, or urinalysis at screening as deemed appropriate by the investigator
  • Subject has a history of substance or alcohol use disorder according to Diagnostic and Statistical Manual of Mental Disorders (5th edition) (DSM-5) criteria within 6 months before screening or positive test result(s) for alcohol and/or drugs of abuse (opiates [including methadone], cocaine, amphetamines, methamphetamines, cannabinoids, barbiturates, ecstasy and benzodiazepines) at screening or admission on Day 1 of each study period
  • Current suicidal or homicidal ideation/intent/behavior
  • Serology positive for hepatitis B surface antigen (HBsAg), hepatitis C antibodies (HCV) or Human immunodeficiency virus (HIV) antibodies

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Randomizowane
  • Model interwencyjny: Zadanie krzyżowe
  • Maskowanie: Podwójnie

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: Group 1 (Sequence ABC)
Participants will receive Treatment A (2 capsules of 20 milligram [mg] JNJ-42847922) in Period 1, Treatment B (10 mg zolpidem and 1 placebo capsule) in Period 2 and Treatment C (2 placebo capsules) in Period 3 with a washout interval of at least 3 days between treatment periods. Participants randomized to this group will be assessed for pharmacodynamic testing at 2 and 6 hours after dosing.
Lek: JNJ-42847922
JNJ-42847922 will be administered as 40 milligram oral capsule (2 capsule*20 mg) in one of the treatment periods.
Lek: Zolpidem
Zolpidem will be administered as 1 capsule containing 10 mg in one of the treatment periods.
Lek: Placebo
Matching Placebo will be administered orally.
Eksperymentalny: Group 2 (Sequence BCA)
Participants will receive Treatment B in Period 1, Treatment C in Period 2 and Treatment A in Period 3 with a washout interval of at least 3 days between treatment periods. Participants randomized to this group will be assessed for pharmacodynamic testing at 2 and 6 hours after dosing.
Lek: JNJ-42847922
JNJ-42847922 will be administered as 40 milligram oral capsule (2 capsule*20 mg) in one of the treatment periods.
Lek: Zolpidem
Zolpidem will be administered as 1 capsule containing 10 mg in one of the treatment periods.
Lek: Placebo
Matching Placebo will be administered orally.
Eksperymentalny: Group 3 (Sequence CAB)
Participants will receive Treatment C in Period 1, Treatment A in Period 2 and Treatment B in Period 3 with a washout interval of at least 3 days between treatment periods. Participants randomized to this group will be assessed for pharmacodynamic testing at 2 and 6 hours after dosing.
Lek: JNJ-42847922
JNJ-42847922 will be administered as 40 milligram oral capsule (2 capsule*20 mg) in one of the treatment periods.
Lek: Zolpidem
Zolpidem will be administered as 1 capsule containing 10 mg in one of the treatment periods.
Lek: Placebo
Matching Placebo will be administered orally.
Eksperymentalny: Group 4 (Sequence ABC)
Participants will receive Treatment A in Period 1, Treatment B in Period 2 and Treatment C in Period 3 with a washout interval of at least 3 days between treatment periods. Participants randomized to this group will be assessed for pharmacodynamic testing at 4 and 8 hours after dosing.
Lek: JNJ-42847922
JNJ-42847922 will be administered as 40 milligram oral capsule (2 capsule*20 mg) in one of the treatment periods.
Lek: Zolpidem
Zolpidem will be administered as 1 capsule containing 10 mg in one of the treatment periods.
Lek: Placebo
Matching Placebo will be administered orally.
Eksperymentalny: Group 5 (Sequence BCA)
Participants will receive Treatment B in Period 1, Treatment C in Period 2 and Treatment A in Period 3 with a washout interval of at least 3 days between treatment periods. Participants randomized to this group will be assessed for pharmacodynamic testing at 4 and 8 hours after dosing.
Lek: JNJ-42847922
JNJ-42847922 will be administered as 40 milligram oral capsule (2 capsule*20 mg) in one of the treatment periods.
Lek: Zolpidem
Zolpidem will be administered as 1 capsule containing 10 mg in one of the treatment periods.
Lek: Placebo
Matching Placebo will be administered orally.
Eksperymentalny: Group 6 (Sequence CAB)
Participants will receive Treatment C in Period 1, Treatment A in Period 2 and Treatment B in Period 3 with a washout interval of at least 3 days between treatment periods. Participants randomized to this group will be assessed for pharmacodynamic testing at 4 and 8 hours after dosing.
Lek: JNJ-42847922
JNJ-42847922 will be administered as 40 milligram oral capsule (2 capsule*20 mg) in one of the treatment periods.
Lek: Zolpidem
Zolpidem will be administered as 1 capsule containing 10 mg in one of the treatment periods.
Lek: Placebo
Matching Placebo will be administered orally.

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Standard Deviation of Lateral Position (SDLP) Assessed From an On-road Driving Test
Ramy czasowe: up to 8 hours post-dose
The SDLP will be measured from a simulated road tracking test over about 15 minutes. Instructed speed is 100 kilometer (km)/hour.
up to 8 hours post-dose

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Mean Lateral Position (MLP) Assessed From an On-road Driving Test
Ramy czasowe: 2 to 8 hours post-dose
The MLP will be measured from a simulated road tracking test over about 15 minutes. Instructed speed is 100 kilometer (km)/hour.
2 to 8 hours post-dose
Distance-keeping Assessed From an On-road Driving Test
Ramy czasowe: 2 to 8 hours post-dose
Distance-keeping will be measured from a simulated road tracking test over about 15 minutes. Instructed speed is 100 kilometer (km)/hour.
2 to 8 hours post-dose
Mean Speed (MS) Assessed From an On-road Driving Test
Ramy czasowe: 2 to 8 hours post-dose
The MS will be measured from a simulated road tracking test over about 15 minutes. Instructed speed is 100 kilometer (km)/hour.
2 to 8 hours post-dose
Standard Deviation of Speed (SDS) Assessed From an On-road Driving Test
Ramy czasowe: 2 to 8 hours post-dose
The SDS will be measured from a simulated road tracking test over about 15 minutes. Instructed speed is 100 kilometer (km)/hour.
2 to 8 hours post-dose
Number of Head movements Assessed From an On-road Driving Test
Ramy czasowe: 2 to 8 hours post-dose
Number of head movements will be measured from a simulated road tracking test over about 15 minutes. Instructed speed is 100 kilometer (km)/hour.
2 to 8 hours post-dose
Reaction-time Assessed From an On-road Driving Test
Ramy czasowe: 2 to 8 hours post-dose
Reaction-time will be assessed by 10 minutes of special and unexpected traffic events.
2 to 8 hours post-dose
Inhibition-time Assessed From an On-road Driving Test
Ramy czasowe: 2 to 8 hours post-dose
Inhibition-time will be assessed by 10 minutes of special and unexpected traffic events.
2 to 8 hours post-dose
Alertness-time Assessed From an On-road Driving Test
Ramy czasowe: 2 to 8 hours post-dose
Alertness-time will be assessed by 10 minutes of special and unexpected traffic events.
2 to 8 hours post-dose
Drive safety Score (DSS)
Ramy czasowe: 2 to 8 hours post-dose
The DSS is a composite score of driving simulator behavior ranging from 0-10, related to actual driving performance.
2 to 8 hours post-dose
Subjective assessment of driving performance using visual analog scale
Ramy czasowe: 2 to 8 hours post-dose
Participants indicated the perceived quality of their driving performance on a visual analog scale, which ranged from 0 ('I drove exceptionally poorly') to 20 ('I drove exceptionally well') around a midpoint of 'I drove normally'.
2 to 8 hours post-dose
Computerized Cognitive Test Battery: Detection (DET) Test
Ramy czasowe: 2 to 8 hours post-dose
Simple reaction time task measuring processing speed; mean of the log10 transformed reaction times for correct responses (lower score = better performance).
2 to 8 hours post-dose
Computerized Cognitive Test Battery: Identification (IDN) Test
Ramy czasowe: 2 to 8 hours post-dose
Choice reaction time paradigm measuring attention; mean of the log10 transformed reaction times for correct responses (lower score = better performance).
2 to 8 hours post-dose
Computerized Cognitive Test Battery: One Back (OBK) Test
Ramy czasowe: 2 to 8 hours post-dose
Working memory measure; mean of the log10 transformed reaction times for correct responses (lower score = better performance).
2 to 8 hours post-dose
Computerized Cognitive Test Battery: One card learning
Ramy czasowe: 2 to 8 hours post-dose
A visual recall test scored using arcsine transformation of the proportion of correct responses.
2 to 8 hours post-dose
Computerized Cognitive Test Battery: Trailmaking Test Form B (TMT-B)
Ramy czasowe: 2 to 8 hours post-dose
TMT-B is a paper-and-pencil measure of divided attention and executive function (tracking, sequencing). The participant is instructed do draw a line to connect a set of 25 consecutively numbered and lettered circles, alternating sequentially between numbers and letters. The participant is instructed to work as quickly as possible while still maintaining accuracy. The test requires approximately 2 minutes to complete, alternate forms are available. Scores include time to completion and errors.
2 to 8 hours post-dose
Postural Stability Test
Ramy czasowe: 2 to 8 hours post-dose
Postural stability will be measured by body sway meter which allows measurement of body movements in a single plane. Body sway is measured with a pot string meter (celesco) based on the Wright ataxiameter (Wright, 1971). With a string attached to the waist, all body movements over a period of time are integrated and expressed as millimeter sway. The total period of body sway measurement will be two minutes.
2 to 8 hours post-dose
Karolinska Sleepiness Scale (KSS) Score
Ramy czasowe: 2 to 8 hours post-dose
The KSS is a participant-reported assessment used to rate sleepiness on a scale of 1 to 9, ranging from 1 (extremely alert) to 9 (very sleepy, great effort to keep awake, fighting sleep).
2 to 8 hours post-dose
Number of Participants With Adverse Events (AEs) and Serious Adverse Events (SAEs)
Ramy czasowe: up to Follow-up (7-10 days after last dose of study drug)
An AE was any untoward medical event that occurs in a participant administered an investigational product, and it does not necessarily indicate only events with clear causal relationship with the relevant investigational product. An SAE was an AE resulting in any of the following outcomes or deemed significant for any other reason: death; initial or prolonged in-patient hospitalization; life-threatening experience (immediate risk of dying); persistent or significant disability/incapacity; congenital anomaly.
up to Follow-up (7-10 days after last dose of study drug)
Relationship between duration of changes in driving ability and plasma concentrations of JNJ-42847922
Ramy czasowe: Pre-dose and Day 1 post-dose
Relationship between duration of changes in driving ability and plasma concentrations of JNJ-42847922 will be reported.
Pre-dose and Day 1 post-dose

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Sponsor

Janssen-Cilag International NV

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów

1 listopada 2015

Zakończenie podstawowe (Rzeczywisty)

1 lutego 2016

Ukończenie studiów (Rzeczywisty)

1 lutego 2016

Daty rejestracji na studia

Pierwszy przesłany

15 października 2015

Pierwszy przesłany, który spełnia kryteria kontroli jakości

15 października 2015

Pierwszy wysłany (Oszacować)

19 października 2015

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Oszacować)

24 marca 2016

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

23 marca 2016

Ostatnia weryfikacja

1 marca 2016

Więcej informacji

Terminy związane z tym badaniem

Słowa kluczowe

Dodatkowe istotne warunki MeSH

Inne numery identyfikacyjne badania

  • CR108056
  • 42847922EDI1011 (Inny identyfikator: Janssen-Cilag International NV)
  • 2015-004203-24 (Numer EudraCT)

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

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