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A Study to Assess the Safety, Tolerability and Pharmacokinetics of ASP3700 in Healthy Male Subjects

29. oktober 2014 opdateret af: Astellas Pharma Europe B.V.

A Phase 1, Single Ascending Oral Dose Study to Assess the Safety, Tolerability and Pharmacokinetics of ASP3700 in Healthy Male Subjects, Including a Drug-drug Interaction Part With Itraconazole

The purpose of this study is to evaluate the safety, tolerability and pharmacokinetics (PK) of single ascending oral doses of ASP3700 in healthy male subjects. This study will also explore the effect of itraconazole (another drug) on the PK of ASP3700, as well as to evaluate the safety and tolerability of ASP3700 alone and in combination with itraconazole in healthy male subjects.

Studieoversigt

Detaljeret beskrivelse

This study consists of 2 parts: Part 1 is a single ascending dose study where subjects will receive either ASP3700 or matching placebo; Part 2 is a drug-drug interaction (DDI) open-label, crossover study comprised of 1 sequence with 2 investigational periods where subjects will receive ASP3700 alone and in combination with itraconazole.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

44

Fase

  • Fase 1

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

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

Ingen

Køn, der er berettiget til at studere

Han

Beskrivelse

Inclusion Criteria:

  • Subject has a body mass index range of 18.5 - 30.0 kg/m2. The subject weighs at least 50 kg.
  • Subject and his female spouse/partners who are of childbearing potential must be using highly effective contraception consisting of 2 forms of birth control (1 of which must be a barrier method) starting at screening and continue throughout the clinical study period and for 90 days after the final study drug administration.
  • Subject must not donate sperm starting at screening and throughout the clinical study period and for 90 days after the final study drug administration.

Exclusion Criteria:

  • Subject has a known or suspected hypersensitivity to ASP3700 (parts 1 and 2) or itraconazole (part 2 only) or significant adverse reactions to historical cannabinoid use or any components of the formulations used.
  • Subject has any of the liver function tests (aspartate aminotransferase [AST], alanine aminotransferase [ALT], alkaline phosphatase, gamma-glutamyl transaminase, total bilirubin [TBL]) above the upper limit of normal (ULN). In such a case the assessment may be repeated once (upon admission to the clinical unit).
  • Subject has a history of a suicide attempt or suicidal behavior. Any recent suicidal ideation within the last 3 months or who are at significant risk to commit suicide, as judged by the Investigator using the C-SSRS (a level of 4 or 5) at screening or upon admission to the clinical unit.
  • Subject has any clinically significant abnormality following the Investigator's review of the physical examination, ECG and clinical study protocol-defined clinical laboratory tests at screening or upon admission to the clinical unit.
  • Subject has a pulse rate < 40 or > 90 beats per minute; mean SBP > 140 mmHg; mean DBP > 90 mmHg (vital signs measurements taken in triplicate after subject has been resting in supine position for 5 minutes; pulse rate will be measured automatically) upon admission to the clinical unit.
  • Subject has a mean corrected QT interval using Fridericia's formula (QTcF) interval > 430 ms at day -1. If the mean QTcF exceeds the limits above, 1 additional triplicate ECG can be taken.
  • Subject has a history of smoking more than 10 cigarettes (or equivalent amount of tobacco) per day within 3 months prior to admission to the clinical unit.
  • Subject has a history of drinking more than 21 units of alcohol per week (1 unit = 10 g pure alcohol = 250 mL of beer [5%] or 35 mL of spirits [35%] or 100 mL of wine [12%]) within 3 months prior to admission to the clinical unit.
  • Subject has consumed grapefruit, grapefruit-containing products or Seville orange-containing products within 72 hours prior to admission to the clinical unit.

Studieplan

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

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Grundvidenskab
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Dobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: ASP3700 single ascending dose cohort
Part 1
oral
Placebo komparator: Placebo single ascending dose cohort
Part 1
mundtlig
Eksperimentel: ASP3700 alone
Part 2
oral
Aktiv komparator: ASP3700 and itraconazole
Part 2
oral
mundtlig

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Safety as assessed by adverse events (Part 1)
Tidsramme: up to end of study visit (up to 16 days)
up to end of study visit (up to 16 days)
Safety as assessed by vital signs (Part 1)
Tidsramme: up to end of study visit (up to 16 days)
up to end of study visit (up to 16 days)
Safety as assessed by laboratory tests (Part 1)
Tidsramme: up to end of study visit (up to 16 days)
Laboratory tests includes the measurement of sex-hormone related biomarkers and exploratory renal biomarkers.
up to end of study visit (up to 16 days)
Safety as assessed by electrocardiogram (ECG) measurements (Part 1)
Tidsramme: up to end of study visit (up to 16 days)
ECG measurements include routine 12-lead ECG, continuous cardiac monitoring (Holter ECG) and real-time cardiac monitoring (ECG telemetry)
up to end of study visit (up to 16 days)
Safety as assessed by Bond and Lader VAS (Part 1)
Tidsramme: Up to Day 2
visual analogue scale (VAS)
Up to Day 2
Safety as assessed by C-SSRS (Part 1)
Tidsramme: Up to end of study visit (up to 16 days)
Columbia - Suicide Severity Rating Scale (C-SSRS)
Up to end of study visit (up to 16 days)
Safety as assessed by ARCI-49 (Part 1)
Tidsramme: Up to Day 2
Addiction Research Center Inventory (ARCI)-49 (49-item)
Up to Day 2
Pharmacokinetic parameter of itraconazole (plasma): Ctrough (Part 2)
Tidsramme: Days 3-13
Concentration immediately prior to dosing at multiple dosing
Days 3-13
Pharmacokinetic parameter of ASP3700 with and without itraconazole (plasma): AUCinf (Part 2)
Tidsramme: Days 1-7 (period 1) and Days 1-13 (period 2)
Area under the concentration-time curve from time of dosing extrapolated to time infinity (AUCinf)
Days 1-7 (period 1) and Days 1-13 (period 2)
Pharmacokinetic parameter of ASP3700 with and without itraconazole (plasma): AUCinf (%extrap) (Part 2)
Tidsramme: Days 1-7 (period 1) and Days 1-13 (period 2)
Percentage of AUCinf due to extrapolation from tlast to time infinity (AUCinf [%extrap])
Days 1-7 (period 1) and Days 1-13 (period 2)
Pharmacokinetic parameter of ASP3700 with and without itraconazole (plasma): AUClast (Part 2)
Tidsramme: Days 1-7 (period 1) and Days 1-13 (period 2)
Area under the concentration-time curve from the time of dosing to the last measurable concentration (AUClast)
Days 1-7 (period 1) and Days 1-13 (period 2)
Pharmacokinetic parameter of ASP3700 with and without itraconazole (plasma): Cmax (Part 2)
Tidsramme: Days 1-7 (period 1) and Days 1-13 (period 2)
Maximum concentration (Cmax)
Days 1-7 (period 1) and Days 1-13 (period 2)
Pharmacokinetic parameter of ASP3700 with and without itraconazole (plasma):λz (Part 2)
Tidsramme: Days 1-7 (period 1) and Days 1-13 (period 2)
Terminal elimination rate constant (λz)
Days 1-7 (period 1) and Days 1-13 (period 2)
Pharmacokinetic parameter of ASP3700 with and without itraconazole (plasma): MRT (Part 2)
Tidsramme: Days 1-7 (period 1) and Days 1-13 (period 2)
Mean residence time (MRT)
Days 1-7 (period 1) and Days 1-13 (period 2)
Pharmacokinetic parameter of ASP3700 with and without itraconazole (plasma): tlag (Part 2)
Tidsramme: Day 1 (period 1 and 2)
Time prior to the time corresponding to the first measurable (nonzero) concentration (tlag)
Day 1 (period 1 and 2)
Pharmacokinetic parameter of ASP3700 with and without itraconazole (plasma): tmax (Part 2)
Tidsramme: Days 1-7 (period 1) and Days 1-13 (period 2)
Time of maximum concentration (tmax)
Days 1-7 (period 1) and Days 1-13 (period 2)
Pharmacokinetic parameter of ASP3700 with and without itraconazole (plasma): t1/2 (Part 2)
Tidsramme: Days 1-7 (period 1) and Days 1-13 (period 2)
Terminal elimination half-life (t1/2)
Days 1-7 (period 1) and Days 1-13 (period 2)
Pharmacokinetic parameter of ASP3700 with and without itraconazole (plasma): Vz/F (Part 2)
Tidsramme: Days 1-7 (period 1) and Days 1-13 (period 2)
Apparent volume of distribution during the terminal elimination phase after extravascular dosing (Vz/F)
Days 1-7 (period 1) and Days 1-13 (period 2)
Pharmacokinetic parameter of ASP3700 with and without itraconazole (urine): Aelast (Part 2)
Tidsramme: Days 1-7 (period 1) and Days 1-13 (period 2)
Cumulative amount of study drug excreted into urine from time of dosing up to the collection time of the last measurable concentration (Aelast)
Days 1-7 (period 1) and Days 1-13 (period 2)
Pharmacokinetic parameter of ASP3700 with and without itraconazole (urine): Aeinf (Part 2)
Tidsramme: Days 1-7 (period 1) and Days 1-13 (period 2)
Cumulative amount of study drug excreted into urine from time of dosing extrapolated to time infinity (Aeinf)
Days 1-7 (period 1) and Days 1-13 (period 2)
Pharmacokinetic parameter of ASP3700 with and without itraconazole (urine): Aelast% (Part 2)
Tidsramme: Days 1-7 (period 1) and Days 1-13 (period 2)
Percentage of study drug excreted into urine from the time of dosing up to the collection time of the last measurable concentration (Aelast%)
Days 1-7 (period 1) and Days 1-13 (period 2)
Pharmacokinetic parameter of ASP3700 with and without itraconazole (urine): Aeinf% (Part 2)
Tidsramme: Days 1-7 (period 1) and Days 1-13 (period 2)
Percentage of study drug excreted into urine from time of dosing extrapolated to time infinity (Aeinf%)
Days 1-7 (period 1) and Days 1-13 (period 2)
Pharmacokinetic parameter of ASP3700 with and without itraconazole (urine): CLR (Part 2)
Tidsramme: Days 1-7 (period 1) and Days 1-13 (period 2)
Renal clearance (CLR)
Days 1-7 (period 1) and Days 1-13 (period 2)
Safety as assessed by orthostatic evaluation (or blood pressure change in orthostatic challenge test) (Part 1)
Tidsramme: Up to Day 7
Up to Day 7

Sekundære resultatmål

Resultatmål
Tidsramme
Composite of pharmacokinetics of ASP3700: AUCinf, AUCinf(%extrap), AUClast, Cmax, CL/F, λz, MRT, tlag, tmax, t½, Vz/F (plasma) (Part 1)
Tidsramme: up to Day 7
up to Day 7
Title: Composite of pharmacokinetics of ASP3700: Aelast, Aeinf, Aelast%, Aeinf%, CLR (urine) (Part 1)
Tidsramme: up to Day 7
up to Day 7
Safety as assessed by adverse events, vital signs, orthostatic evaluation, laboratory tests, ECG measurements, C-SSRS, Bond & Lader VAS, ARCI-49 (Part 2)
Tidsramme: Days 1-7 (period 1) and Days 1-13 (period 2) and at end of study visit (up to 22 days)
Days 1-7 (period 1) and Days 1-13 (period 2) and at end of study visit (up to 22 days)

Samarbejdspartnere og efterforskere

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

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. maj 2014

Primær færdiggørelse (Faktiske)

1. oktober 2014

Studieafslutning (Faktiske)

1. oktober 2014

Datoer for studieregistrering

Først indsendt

28. maj 2014

Først indsendt, der opfyldte QC-kriterier

2. juni 2014

Først opslået (Skøn)

4. juni 2014

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

30. oktober 2014

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

29. oktober 2014

Sidst verificeret

1. oktober 2014

Mere information

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 .

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