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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 bijgewerkt door: 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

Studie Overzicht

Studietype

Ingrijpend

Inschrijving (Werkelijk)

20

Fase

  • Fase 1

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

18 jaar tot 65 jaar (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Ja

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

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

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Crossover-opdracht
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: BI 1356

Treatment sequence AB_C or C_AB

  • Treatment A: 5 days BI 1356 until steady state followed by
  • Treatment B: combined treatment of BI 1356 with pioglitazone for 7 days
  • Treatment C: 7 days of treatment with Pioglitazone alone
Actieve vergelijker: Pioglitazone

Treatment sequence AB_C or C_AB

  • Treatment A: 5 days BI 1356 until steady state followed by
  • Treatment B: combined treatment of BI 1356 with pioglitazone for 7 days
  • Treatment C: 7 days of treatment with Pioglitazone alone

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Tijdsspanne
AUCτ,ss (area under the concentration-time curve of the analyte in plasma at steady state over a uniform dosing interval τ)
Tijdsspanne: 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)
Tijdsspanne: up to 21 days
up to 21 days

Secundaire uitkomstmaten

Uitkomstmaat
Tijdsspanne
tmax,ss (time from last dosing to maximum concentration of the analyte in plasma at steady state)
Tijdsspanne: 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)
Tijdsspanne: up to 21 days
up to 21 days
λz,ss (terminal rate constant in plasma at steady state)
Tijdsspanne: up to 21 days
up to 21 days
t1/2,ss (terminal half-life of the analyte in plasma at steady state)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: up to 21 days
up to 21 days
Changes in physical examination (including body weight)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: up to 27 days after last administration of study medication
up to 27 days after last administration of study medication

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

Nuttige links

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start

1 februari 2007

Primaire voltooiing (Werkelijk)

1 april 2007

Studieregistratiedata

Eerst ingediend

4 juli 2014

Eerst ingediend dat voldeed aan de QC-criteria

4 juli 2014

Eerst geplaatst (Schatting)

8 juli 2014

Updates van studierecords

Laatste update geplaatst (Schatting)

8 juli 2014

Laatste update ingediend die voldeed aan QC-criteria

4 juli 2014

Laatst geverifieerd

1 juli 2014

Meer informatie

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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