- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02276378
Influence of Food on the Bioavailability of Two Doses of Telmisartan/HCTZ Fixed-dose Combination in Japanese Healthy Male Volunteers
27. oktober 2014 opdateret af: Boehringer Ingelheim
Influence of Food on the Bioavailability of Telmisartan 40 mg/HCTZ 12.5 mg Fixed-dose Combination and of Telmisartan 80 mg/HCTZ 12.5 mg Fixed-dose Combination in Japanese Healthy Male Volunteers (an Open-label, Randomised, Single-dose, Two-way Crossover Study)
To investigate the relative bioavailability and pharmacokinetics of the fixed-dose combination tablets (telmisartan 40 mg/HCTZ 12.5 mg and telmisartan 80 mg/HCTZ 12.5 mg) after food intake in comparison with those in the fasting state in healthy Japanese male volunteers
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
32
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
20 år til 35 år (Voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Han
Beskrivelse
Inclusion Criteria:
Healthy males according to the following criteria:
- Based upon a complete medical history, including the physical examination, vital signs (blood pressure (BP), pulse rate (PR), body temperature), 12-lead ECG (electrocardiogram), clinical laboratory tests
- Age ≥20 and Age ≤35 years
- Body weight ≥50 kg
- BMI ≥18.0 and BMI ≤25.0 kg/m2 (Body Mass Index)
- Signed and dated written informed consent prior to admission to the study in accordance with Good clinical practice (GCP) and the local legislation.
Exclusion Criteria:
- Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders
- Diseases of the central nervous system (such as epilepsy) or psychiatric disorders or neurological disorders
- Chronic or relevant acute infections
- Any clinical relevant findings of the laboratory test deviating from normal
- Positive result for either hepatitis B surface (HBs) antigen, anti Hepatitis C virus (HCV) antibodies, syphilitic test or human immunodeficiency virus (HIV) test
- History of surgery of gastrointestinal tract (except appendectomy)
- History of relevant orthostatic hypotension, fainting spells or blackouts
- Known hypersensitivity to any component of the formulation (telmisartan and hydrochlorothiazide), or to any other angiotensin II receptor blocker (ARBs), any other thiazides, or thiazide derivatives (e.c. sulfonamide derivatives like a chlorthalidone)
- Intake of drugs with a long half-life (≥24 hours) within at least one month or less than 10 half-lives of the respective drug prior to administration or during the trial
- Use of drugs which might reasonably influence the results of the trial based on the knowledge at the time of protocol preparation within 7 days prior to administration or during the trial
- Participation in another trial with an investigational drug within 4 months or 6 half-lives of the investigational drug prior to administration
- Smoker (≥20 cigarettes/day)
- Alcohol abuse (60 g or more ethanol/day: ex. 3 middle-sized bottles of beer, 3 gous (equivalent to 540 mL) of sake)
- Drug abuse
- Blood donation (more than 100 mL within 4 weeks prior to administration or during the trial)
- Excessive physical activities (within 1 week prior to administration or during the trial)
- Intake of alcohol within 2 days prior to administration
- Inability to comply with dietary regimen of study centre
- Inability to refrain from smoking on trial days
- Subjects judged to be inappropriate by the investigator or the sub-investigator
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: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Telmisartan low / HCTZ fixed-dose combination, fed
|
|
|
Eksperimentel: Telmisartan high / HCTZ fixed-dose combination, fed
|
|
|
Aktiv komparator: Telmisartan low /HCTZ fixed-dose combination, fasted
|
|
|
Aktiv komparator: Telmisartan high /HCTZ fixed-dose combination, fasted
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Area under the concentration-time curve of the analyte in the plasma over the time interval from 0 to the time of the last quantifiable data point (AUC0-tz)
Tidsramme: Up to 72 hours after drug administration
|
Up to 72 hours after drug administration
|
|
The maximum measured concentration of the analyte in the plasma (Cmax)
Tidsramme: Up to 72 hours after drug administration
|
Up to 72 hours after drug administration
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Antal deltagere med klinisk signifikante fund i vitale tegn
Tidsramme: Op til 72 timer efter sidste lægemiddeladministration
|
Op til 72 timer efter sidste lægemiddeladministration
|
|
Gennemsnitlig opholdstid for analytten i kroppen efter oral administration (MRTpo)
Tidsramme: Op til 72 timer efter lægemiddeladministration
|
Op til 72 timer efter lægemiddeladministration
|
|
Area under the concentration-time curve of the analyte in the plasma over the time interval from 0 extrapolated to infinity (AUC0-∞)
Tidsramme: Up to 72 hours after drug administration
|
Up to 72 hours after drug administration
|
|
Time from dosing to the maximum concentration of the analyte in the plasma (tmax)
Tidsramme: Up to 72 hours after drug administration
|
Up to 72 hours after drug administration
|
|
Terminal rate constant in the plasma (λz)
Tidsramme: Up to 72 hours after drug administration
|
Up to 72 hours after drug administration
|
|
Terminal half-life of the analyte in the plasma (t1/2)
Tidsramme: Up to 72 hours after drug administration
|
Up to 72 hours after drug administration
|
|
Number of participants with abnormal findings in physical examination
Tidsramme: Up to 72 hours after drug administration
|
Up to 72 hours after drug administration
|
|
Number of participants with clinically significant findings in 12-lead ECG
Tidsramme: Up to 72 hours after drug administration
|
Up to 72 hours after drug administration
|
|
Number of participants with clinically significant findings in clinical laboratory parameters
Tidsramme: Up to 72 hours after drug administration
|
Up to 72 hours after drug administration
|
|
Number of participants with adverse events
Tidsramme: Up to 7 days after drug administration
|
Up to 7 days after drug administration
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Hjælpsomme links
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. juli 2008
Primær færdiggørelse (Faktiske)
1. august 2008
Datoer for studieregistrering
Først indsendt
27. oktober 2014
Først indsendt, der opfyldte QC-kriterier
27. oktober 2014
Først opslået (Skøn)
28. oktober 2014
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
28. oktober 2014
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
27. oktober 2014
Sidst verificeret
1. oktober 2014
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Lægemidlers fysiologiske virkninger
- Molekylære mekanismer for farmakologisk virkning
- Antihypertensive midler
- Natriuretiske midler
- Membrantransportmodulatorer
- Diuretika
- Angiotensin II Type 1-receptorblokkere
- Angiotensinreceptorantagonister
- Natriumchlorid Symporter-hæmmere
- Hydrochlorthiazid
- Telmisartan
Andre undersøgelses-id-numre
- 502.569
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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