- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01402076
A Study to Assess the Effect Tasimelteon on the Cytochrome P450 3A4 and 2C8 Enzymes in Healthy Subjects
An Open-Label, Single-Sequence Study to Assess the Effect of Multiple Doses of Tasimelteon on the Cytochrome P450 3A4 and 2C8 Enzymes Using Midazolam and Rosiglitazone as Substrates in Healthy Subjects
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Fase 1
Kontakter og lokationer
Studiesteder
-
-
Missouri
-
Springfield, Missouri, Forenede Stater, 65802
- Bio-Kinetic Clinical Applications
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Ability and acceptance to provide written informed consent;
- Subjects must be males or females between 18 and 55 years of age, inclusive;
Female subjects of childbearing potential must be non-pregnant and non-lactating and have a negative serum or urine pregnancy test at the Screening visit and at Check-in (Days -1) and agree not to attempt to become pregnant during the course of the study. Female subjects of childbearing potential (including peri-menopausal women who have had a menstrual bleeding within 1 year) must be using appropriate birth control (e.g. intrauterine device [IUD], diaphragm or condom with spermicidal jelly or foam or abstinence, or cervical cap) for a period of 35 days before the first dosing, for the duration of the study, and for one month after the last dose;
a. Note: Women are not permitted to use hormonal methods of birth control (e.g. oral contraceptives, hormonal intrauterine device [IUD], patch and steroids) and must use another acceptable method of birth control during the study and for one month after the last dose. Women currently taking oral contraceptives will be required to discontinue their regimen two weeks prior to first dosing.
- Subjects with Body Mass Index (BMI) of >18 and <35 kg/m2 (BMI = weight (kg)/ [height (m)]2);
Vital signs (after 3 minutes resting in a semi-supine position) which are within the ranges shown below:
- Body temperature between 35.0-37.5 °C;
- Systolic blood pressure between 90-150 mm Hg;
- Diastolic blood pressure between 50-95 mm Hg;
- Pulse rate between 50-100 bpm.
- Willing and able to comply with study requirements;
- Subjects must be in good health as determined by past medical history, physical examination, electrocardiogram, clinical laboratory tests and urinalysis;
Exclusion Criteria:
- History of recent (within six months) drug or alcohol abuse;
- Any major surgery within three months of Day 1 or any minor surgery within one month;
- Donation or loss of 400 mL or more of blood within two months prior to the Baseline Visit;
- History or current evidence of cardiovascular, hepatic, hematopoietic, renal, gastrointestinal or metabolic dysfunction judged by the Investigator to be clinically significant;
- Any condition requiring the regular use of medication;
- History of intolerance and/or hypersensitivity to drugs including midazolam, rosiglitazone or other 'glitazones', melatonin or melatonin agonists, or anyone who has taken a melatonin preparation chronically within the past two months prior to Day 1;
- History of or current evidence of hypoglycemia judged by the Investigator to be clinically significant;
- History of liver disease and/or positive for one or more of the following serological results: HCV, HIV, HBsAg
- Treatment with any drug known to cause major organ system toxicity (e.g., chloramphenicol or tamoxifen) during the 60 day preceding Day 1;
- Elevated (> 2 times the upper limit of normal) liver function tests (i.e. aspartate aminotransferase (AST [SGOT]), alanine aminotransferase (ALT [SGPT]), and total bilirubin);
- Inability to be venipunctured and/or tolerate venous access;
- Subjects who have used tobacco products 3 months prior to dosing.
- Exposure to any investigational drug within 30 days or 5 half lives (whichever is longer) of baseline, including placebo;
- Participation in a previous BMS-214778/VEC-162 trial;
- Use of prescription or OTC medication, including herbal products (e.g., St. John's Wort) within 2 weeks of Day 1;
- Use of any food or beverage containing alcohol, grapefruit or grapefruit juice, apple or orange juice, vegetables from the mustard green family (e.g. kale, broccoli, watercress, collard greens, kohlrabi, brussel sprouts, mustard) and charbroiled meats within 1 week before Day 1 and during the actual duration of the study;
- Any other sound medical reason as determined by the clinical Investigator.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Grundvidenskab
- Tildeling: Ikke-randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Steady State PK Group
|
20mg daily dosing, Days 4-20
4mg, single dose, Days 3 and 20
Andre navne:
10mg, single dose, Days 1 and 18
|
|
Eksperimentel: No steady state PK
|
20mg daily dosing, Days 4-20
4mg, single dose, Days 3 and 20
Andre navne:
10mg, single dose, Days 1 and 18
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
CYP3A4 Pharmacokinetics
Tidsramme: Days 1 and 18
|
Composite of 24 hour pharmacokinetic parameters of midazolam will be compared between Day 1 and Day 18.
|
Days 1 and 18
|
|
CYP2C8 Pharmacokinetics
Tidsramme: Days 3 and 20
|
Composite of 24 hour pharmacokinetic parameters of rosiglitazone will be compared between Day 3 and 20.
|
Days 3 and 20
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Midazolam PK
Tidsramme: Days 1 and 17
|
Composite pharmacokinetic parameters of midazolam and α-hydroxymidazolam will be compared between Day 1 and Day 18.
|
Days 1 and 17
|
|
Rosiglitazone PK
Tidsramme: Days 3 and 20
|
Composite of 24 hour pharmacokinetic parameters of rosiglitazone will be compared between Day 3 and Day 20.
|
Days 3 and 20
|
|
Tasimelteon multiple dose pharmacokinetics
Tidsramme: Days 4-21
|
Composite of 24 hour pharmacokinetic parameters of tasimelteon and tasimelteon metabolites M9, M11, M12, M13, and M14, at Days 5, 8, 11, 14 (Group 1 only), and Days 17 and 19 (Groups 1 and 2).
|
Days 4-21
|
|
Tasimelteon safety and tolerability
Tidsramme: Days 1-21
|
Safety of multiple oral doses of 20 mg of tasimelteon alone and in combination with 10 mg of midazolam as measured by vital signs, ECG, and adverse event reporting.
|
Days 1-21
|
Samarbejdspartnere og efterforskere
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
- Hypoglykæmiske midler
- Lægemidlers fysiologiske virkninger
- Neurotransmittermidler
- Molekylære mekanismer for farmakologisk virkning
- Depressive midler til centralnervesystemet
- Bedøvelsesmidler, intravenøst
- Bedøvelsesmidler, general
- Bedøvelsesmidler
- Beroligende midler
- Psykotropiske stoffer
- Hypnotika og beroligende midler
- Adjuvanser, anæstesi
- Anti-angst midler
- GABA modulatorer
- GABA agenter
- Midazolam
- Rosiglitazon
Andre undersøgelses-id-numre
- VP-VEC-162-1110
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 Tasimelteon
-
Vanda PharmaceuticalsRekrutteringSøvnforstyrrelse | Søvnforstyrrelser | Autismespektrumforstyrrelse | Neurologisk lidelseForenede Stater
-
Vanda PharmaceuticalsAfsluttet
-
Vanda PharmaceuticalsAfsluttet
-
Vanda PharmaceuticalsAfsluttetJetlag lidelseForenede Stater
-
Vanda PharmaceuticalsRekrutteringSøvnvågningsforstyrrelser | Søvnforstyrrelser, døgnrytme | Kronobiologiske lidelser | Genmutationer og andre ændringer NecKalkun
-
Vanda PharmaceuticalsRekrutteringSøvnvågningsforstyrrelser | Søvnforstyrrelser, døgnrytme | Kronobiologiske lidelserForenede Stater, Tyskland, Østrig
-
Vanda PharmaceuticalsAfsluttetJetlag type søvnløshedForenede Stater
-
Brigham and Women's HospitalVanda PharmaceuticalsAfsluttetREM-adfærdsforstyrrelseForenede Stater
-
Vanda PharmaceuticalsAfsluttetSmith-Magenis syndrom | CirkadiskForenede Stater
-
Vanda PharmaceuticalsAfsluttetIkke-24-timers søvn-vågen lidelse