Denne siden ble automatisk oversatt og nøyaktigheten av oversettelsen er ikke garantert. Vennligst referer til engelsk versjon for en kildetekst.

Influence of Food on the Bioavailability of Two Doses of Telmisartan/HCTZ Fixed-dose Combination in Japanese Healthy Male Volunteers

27. oktober 2014 oppdatert av: 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

Studieoversikt

Studietype

Intervensjonell

Registrering (Faktiske)

32

Fase

  • Fase 1

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

20 år til 35 år (Voksen)

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Mann

Beskrivelse

Inclusion Criteria:

Healthy males according to the following criteria:

  1. 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
  2. Age ≥20 and Age ≤35 years
  3. Body weight ≥50 kg
  4. BMI ≥18.0 and BMI ≤25.0 kg/m2 (Body Mass Index)
  5. 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:

  1. Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders
  2. Diseases of the central nervous system (such as epilepsy) or psychiatric disorders or neurological disorders
  3. Chronic or relevant acute infections
  4. Any clinical relevant findings of the laboratory test deviating from normal
  5. Positive result for either hepatitis B surface (HBs) antigen, anti Hepatitis C virus (HCV) antibodies, syphilitic test or human immunodeficiency virus (HIV) test
  6. History of surgery of gastrointestinal tract (except appendectomy)
  7. History of relevant orthostatic hypotension, fainting spells or blackouts
  8. 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)
  9. 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
  10. 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
  11. Participation in another trial with an investigational drug within 4 months or 6 half-lives of the investigational drug prior to administration
  12. Smoker (≥20 cigarettes/day)
  13. Alcohol abuse (60 g or more ethanol/day: ex. 3 middle-sized bottles of beer, 3 gous (equivalent to 540 mL) of sake)
  14. Drug abuse
  15. Blood donation (more than 100 mL within 4 weeks prior to administration or during the trial)
  16. Excessive physical activities (within 1 week prior to administration or during the trial)
  17. Intake of alcohol within 2 days prior to administration
  18. Inability to comply with dietary regimen of study centre
  19. Inability to refrain from smoking on trial days
  20. Subjects judged to be inappropriate by the investigator or the sub-investigator

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Crossover-oppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Telmisartan low / HCTZ fixed-dose combination, fed
Eksperimentell: 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

Hva måler studien?

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
Antall deltakere med klinisk signifikante funn i vitale tegn
Tidsramme: Inntil 72 timer etter siste legemiddeladministrering
Inntil 72 timer etter siste legemiddeladministrering
Gjennomsnittlig oppholdstid for analytten i kroppen etter oral administrering (MRTpo)
Tidsramme: Inntil 72 timer etter legemiddeladministrering
Inntil 72 timer etter legemiddeladministrering
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

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Hjelpsomme linker

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart

1. juli 2008

Primær fullføring (Faktiske)

1. august 2008

Datoer for studieregistrering

Først innsendt

27. oktober 2014

Først innsendt som oppfylte QC-kriteriene

27. oktober 2014

Først lagt ut (Anslag)

28. oktober 2014

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

28. oktober 2014

Siste oppdatering sendt inn som oppfylte QC-kriteriene

27. oktober 2014

Sist bekreftet

1. oktober 2014

Mer informasjon

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

Kliniske studier på Sunn

Kliniske studier på Telmisartan lav

3
Abonnere