Denne side blev automatisk oversat, og nøjagtigheden af ​​oversættelsen er ikke garanteret. Der henvises til engelsk version for en kildetekst.

A Study to Demonstrate Bioequivalence Between a 12-mg Dose of an Oral Suspension Formulation of Perampanel and a 12-mg Tablet Formulation of Perampanel Under Fasted and Fed Conditions in Healthy Subjects

2. november 2015 opdateret af: Eisai Inc.

A Randomized, Open-Label, Crossover Study to Demonstrate Bioequivalence Between a 12-mg Dose of an Oral Suspension Formulation of Perampanel and a 12-mg Tablet Formulation of Perampanel Under Fasted and Fed Conditions in Healthy Subjects

This is an open-label, 2-arm, single-dose, randomized crossover study. The study will enroll a total of 100 subjects (2 arms with 50 subjects in each arm). In Arm 1, bioequivalence between the oral suspension and tablet formulations of perampanel will be evaluated under fasted conditions; in Arm 2, bioequivalence between the oral suspension and tablet formulations will be evaluated under fed conditions. In both study arms, subjects will be randomized on Study Day 1 for Treatment Period 1 to receive a single 12-mg dose for perampanel as either oral suspension or a tablet, and will then receive the alternative treatment on Study Day 43 of Treatment Period 2. Drug administration will be separated by a washout of at least 6 weeks between the two treatment periods.

Studieoversigt

Status

Afsluttet

Betingelser

Intervention / Behandling

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

100

Fase

  • Fase 1

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år til 55 år (Voksen)

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria

  1. Healthy males or females, ages 18 to 55 years, inclusive, at the time of informed consent.
  2. Body mass index (BMI) of 18 to 32 kg/m2, inclusive at Screening.
  3. Females must not be lactating or pregnant at Screening or Baseline.
  4. Females of childbearing potential must not have had unprotected sexual intercourse within 30 days before study entry and must agree to use a highly effective method of contraception (eg, total abstinence, a doublebarrier method [such as condom plus diaphragm with spermicide], have a vasectomized partner with confirmed azoospermia, or an intrauterine device, contraceptive implant, or oral contraceptive that does not contain levogesterol) throughout the entire study period and for 30 days after study drug discontinuation. Females using hormonal contraceptives containing levogesterol must be on another form of contraception (such as double barrier method.) as well. If currently abstinent, the subject must agree to use a doublebarrier method as described above if she becomes sexually active during the study period or for 30 days after study drug discontinuation. Females who are using hormonal contraceptives must have been on a stable dose of the same hormonal contraceptive product for at least 4 weeks before dosing and must continue to use the same contraceptive during the study and for 30 days after study drug discontinuation. All females will be considered to be of childbearing potential unless they are postmenopausal (amenorrheic for at least 12 consecutive months, in the appropriate age group, and without other known or suspected cause) or have been sterilized surgically (i.e. bilateral tubal ligation, total hysterectomy, or bilateral oophorectomy, all with surgery at least 1 month before dosing).

Exclusion Criteria

  1. Clinically significant illness that requires medical treatment within 8 weeks or a clinically significant infection that requires medical attention within 4 weeks of dosing.
  2. Evidence of disease that may influence the outcome of the study within 4 weeks of dosing, eg, psychiatric disorders and disorders of the gastrointestinal tract, liver, kidney, respiratory system, endocrine system, hematological system, neurological system, cardiovascular system, or subjects who have a congenital abnormality in metabolism.
  3. Any history of gastrointestinal surgery that may affect PK profiles of perampanel, eg, hepatectomy, nephrotomy, cholecystectomy, digestive organ resection or any gastrointestinal procedure for the purpose of weight loss (including Lapband), which would slow gastric emptying.
  4. Any clinically abnormal symptom or organ impairment found by medical history at Screening, and physical examinations, vital signs, electrocardiogram (ECG) finding, or laboratory test results that require medical treatment at Screening or Baseline.
  5. Any laboratory abnormalities considered clinically significant by the investigator.
  6. A prolonged QT/QTc interval (QTc greater than 450 msec) as demonstrated upon repeat ECG at Screening or Baseline.
  7. History of prolonged QT/QTc interval.
  8. History of risk factors for torsade de pointes (eg, heart failure, hypokalemia, family history of long QT syndrome).
  9. History of ischemic heart disease (eg, acute coronary syndromes, stable angina), syncope or cardiac arrhythmias.
  10. Siting heart rate less than 40 or greater than 100 beats/min at Screening or Baseline Period 1 and sitting systolic blood pressure greater than 140 mmHg or less than 90 mmHg or diastolic blood pressure greater than 90 mmHg or less than 60 mmHg at Screening or Baseline.
  11. Hemoglobin less than 11.5 g/dLfor females and less than 12.5 g/dL for males at screen and Baseline check-in Period 1.
  12. Subjects who experienced a weight loss or gain of greater than 10% between Screening and before dosing.
  13. Subjects who received blood products within 4 weeks, donated blood within 8 weeks, or donated plasma within 1 week of dosing.
  14. Hypersensitivity to the study drug or any of its excipients.
  15. Known history of food allergies or presently experiencing significant seasonal or perennial allergy at Screening.
  16. Known to be human immunodeficiency virus (HIV) positive at Screening.
  17. Active viral hepatitis (B or C) as demonstrated by positive serology at Screening.
  18. History of use of illegal (or legalized) recreational drugs in the past year.
  19. History of drug or alcohol dependency or abuse within approximately the last 2 years or who have a positive urine drug test or breath alcohol test at Screening or Baseline.
  20. Engagement in strenuous exercise within 2 weeks before dosing (eg, marathon runners, weight lifters).
  21. Currently enrolled in another clinical trial or used any investigational drug or device within 30 days preceding informed consent.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Crossover opgave
  • Maskning: Dobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Perampanel - Group 1

Treatment A: Single oral dose of a 12-mg perampanel tablet under fasted condition.

Treatment B: Single 12 mg dose of perampanel oral suspension under fasted condition.

Subjects will be randomized on Study Day 1 for Treatment Period 1 to Treatment A or Treatment B. On Study Day 43 the subject will then receive the alternate Treatment for Treatment Period 2.

Eksperimentel: Perampanel - Group 2

Treatment C: Single oral dose of a 12-mg perampanel tablet co-administered with high fat meal.

Treatment D: Single 12 mg dose of perampanel oral suspension co-administered with high fat meal.

Subjects will be randomized on Study Day 1 for Treatment Period 1 to Treatment C or Treatment D. On Study Day 43 the subject will then receive the alternate Treatment for Treatment Period 2.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Tidsramme
Pharmacokinetics of Perampanel: AUC(0-t)
Tidsramme: Up to 504 hours postdose in each treatment period
Up to 504 hours postdose in each treatment period
Pharmacokinetics of Perampanel: AUC(0-inf)
Tidsramme: Up to 504 hours postdose in each treatment period
Up to 504 hours postdose in each treatment period
Pharmacokinetics of Perampanel: Cmax
Tidsramme: Up to 504 hours postdose in each treatment period
Up to 504 hours postdose in each treatment period

Sekundære resultatmål

Resultatmål
Tidsramme
Pharmacokinetics of Perampanel: AUC(0-72h)
Tidsramme: Up to 504 hours postdose in each treatment period
Up to 504 hours postdose in each treatment period
Pharmacokinetics of Perampanel: tmax
Tidsramme: Up to 504 hours postdose in each treatment period
Up to 504 hours postdose in each treatment period
Pharmacokinetics of Perampanel: tlag
Tidsramme: Up to 504 hours postdose in each treatment period
Up to 504 hours postdose in each treatment period
Pharmacokinetics of Perampanel: Lambda-z
Tidsramme: Up to 504 hours postdose in each treatment period
Up to 504 hours postdose in each treatment period
Pharmacokinetics of Perampanel: t1/2
Tidsramme: Up to 504 hours postdose in each treatment period
Up to 504 hours postdose in each treatment period

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart

1. september 2014

Primær færdiggørelse (Faktiske)

1. december 2014

Studieafslutning (Faktiske)

1. januar 2015

Datoer for studieregistrering

Først indsendt

15. oktober 2014

Først indsendt, der opfyldte QC-kriterier

29. oktober 2014

Først opslået (Skøn)

31. oktober 2014

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

3. november 2015

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

2. november 2015

Sidst verificeret

1. november 2015

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • E2007-A001-048

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Kliniske forsøg med Perampanel

3
Abonner