- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02183337
Bioavailability of BI 1356 With and Without Co-administration of Pioglitazone and the Bioavailability of Pioglitazone With and Without Coadministration of BI 1356 in Healthy Male and Female Volunteers
4. juli 2014 opdateret af: Boehringer Ingelheim
Relative Bioavailability of Both BI 1356 and Pioglitazone After Co-administration Compared to the Bioavailability of Multiple Oral Doses of BI 1356 10 mg qd Alone and Pioglitazone 45 mg qd Alone in Healthy Male and Female Volunteers (an Open Label, Randomised, Multiple-dose, Two-way Crossover Study)
Study to investigate the bioavailability of BI 1356 with and without co-administration of pioglitazone and the bioavailability of pioglitazone with and without coadministration of BI 1356
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
20
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 65 år (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Healthy females and males according to the following criteria: Based upon a complete medical history, including the physical examination, vital signs (Blood Pressure (BP), Pulse Rate (PR)), 12-lead Electrocardiogram (ECG), clinical laboratory tests
- Age ≥18 and Age ≤65 years
- BMI ≥18.5 and BMI ≤29.9 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:
- Any finding of the medical examination (including BP, PR and ECG) deviating from normal and of clinical relevance
- Any evidence of a clinically relevant concomitant disease
- Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders
- Surgery of the gastrointestinal tract (except appendectomy)
- Diseases of the central nervous system (such as epilepsy) or psychiatric disorders or neurological disorders
- History of relevant orthostatic hypotension, fainting spells or blackouts
- Chronic or relevant acute infections (e.g. HIV)
- History of relevant allergy/hypersensitivity (including allergy to drug or its excipients)
- 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 or that prolong the QT/QTc interval based on the knowledge at the time of protocol preparation within 10 days prior to administration or during the trial
- Participation in another trial with an investigational drug within two months prior to administration or during the trial
- Smoker (> 10 cigarettes or > 3 cigars or > 3 pipes/day)
- Inability to refrain from smoking on trial days
- Alcohol abuse (more than 60 g/day)
- Drug abuse
- Blood donation (more than 100 mL within four weeks prior to administration or during the trial)
- Excessive physical activities (within one week prior to administration or during the trial)
- Any laboratory value outside the reference range that is of clinical relevance
- Inability to comply with dietary regimen of trial site
- A marked baseline prolongation of QT/QTc interval (e.g., repeated demonstration of a QTc interval >450 ms)
- A history of additional risk factors for Torsade de Pointes (TdP) (e.g., heart failure, hypokalemia, family history of Long QT Syndrome)
For male subjects:
- Not willing to use adequate contraception (condom use plus another form of contraception e.g. spermicide, oral contraceptive taken by female partner, sterilisation, IUD [intrauterine device]) during the whole study period from the time of the first intake of study drug until one month after the last intake
For female subjects:
- Pregnancy or planning to become pregnant within 2 months of study completion
- Positive pregnancy test
- Are not willing or are unable to use a reliable method of contraception (such as implants, injectibles and combined oral contraceptives, sterilisation, IUD, double barrier method) for at least 3 months prior to participation in the trial, during and up to 2 months after completion/termination of the trial
- Chronic use of oral contraception or hormone replacement containing ethinyl estradiol as the only method of contraception
- Lactation period
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: BI 1356
Treatment sequence AB_C or C_AB
|
|
|
Aktiv komparator: Pioglitazone
Treatment sequence AB_C or C_AB
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
AUCτ,ss (area under the concentration-time curve of the analyte in plasma at steady state over a uniform dosing interval τ)
Tidsramme: up to 21 days
|
up to 21 days
|
|
Cmax,ss (maximum measured concentration of the analyte in plasma at steady state over a uniform dosing interval τ)
Tidsramme: up to 21 days
|
up to 21 days
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
tmax,ss (time from last dosing to maximum concentration of the analyte in plasma at steady state)
Tidsramme: up to 21 days
|
up to 21 days
|
|
C24,ss (concentration of the analyte in plasma at steady state after administration of the last dose at the end of the dosing interval)
Tidsramme: up to 21 days
|
up to 21 days
|
|
λz,ss (terminal rate constant in plasma at steady state)
Tidsramme: up to 21 days
|
up to 21 days
|
|
t1/2,ss (terminal half-life of the analyte in plasma at steady state)
Tidsramme: up to 21 days
|
up to 21 days
|
|
MRTpo,ss (mean residence time of the analyte in the body at steady state after oral administration)
Tidsramme: up to 21 days
|
up to 21 days
|
|
CL/F,ss (apparent clearance of the analyte in the plasma after extravascular administration at steady state)
Tidsramme: up to 21 days
|
up to 21 days
|
|
Vz/F,ss (apparent volume of distribution during the terminal phase λz at steady state following extravascular administration)
Tidsramme: up to 21 days
|
up to 21 days
|
|
Changes in physical examination (including body weight)
Tidsramme: up to 27 days after last administration of study medication
|
up to 27 days after last administration of study medication
|
|
Changes in Vital signs (Blood pressure (BP), Pulse Rate (PR)
Tidsramme: up to 27 days after last administration of study medication
|
up to 27 days after last administration of study medication
|
|
Changes in 12-lead ECG (electrocardiogram)
Tidsramme: up to 27 days after last administration of study medication
|
up to 27 days after last administration of study medication
|
|
Changes in clinical laboratory values
Tidsramme: up to 27 days after last administration of study medication
|
up to 27 days after last administration of study medication
|
|
Number of patients with adverse events
Tidsramme: up to 27 days after last administration of study medication
|
up to 27 days after last administration of study medication
|
|
Assessment of tolerability by investigator on a 4-point scale
Tidsramme: up to 27 days after last administration of study medication
|
up to 27 days after last administration of study medication
|
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. februar 2007
Primær færdiggørelse (Faktiske)
1. april 2007
Datoer for studieregistrering
Først indsendt
4. juli 2014
Først indsendt, der opfyldte QC-kriterier
4. juli 2014
Først opslået (Skøn)
8. juli 2014
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
8. juli 2014
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
4. juli 2014
Sidst verificeret
1. juli 2014
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 1218.13
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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