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Pharmacokinetics, Pharmacodynamics, Safety and Tolerability of Single and Multiple Doses of Linagliptin Tablets in Patients With Different Degrees of Renal Impairment in Comparison to Subjects With Normal Renal Function

15. juli 2014 opdateret af: Boehringer Ingelheim

Pharmacokinetics, Pharmacodynamics, Safety and Tolerability of Single and Multiple 5 mg Doses of Linagliptin Tablets in Patients With Different Degrees of Renal Impairment in Comparison to Subjects With Normal Renal Function in a Monocentric, Open, Parallel-group, Phase I Trial

The main objective of this study was to assess the effect of normal and impaired renal function on the safety, pharmacokinetics, and pharmacodynamics of linagliptin following oral administration of 5 mg daily for 7 days (Groups 1 to 3), 5 mg daily for 10 days (Groups 6 and 7), or as a single dose (Groups 4 and 5)

Studieoversigt

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

51

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 80 år (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • Male or female subjects with normal renal function, defined as a Creatinine Clearance (CrCl) of >80 mL/min on screening (Group 1) , or male or female patients with Type 2 diabetes mellitus (T2DM) and normal renal function, defined as a CrCl of >80 mL/min on screening (Group 7)
  • Male or female patients with Renal impairment (RI), determined by the value of CrCl on Screening estimated according to the Cockcroft-Gault formula. Patients were classified into groups by their CrCl values:

    • Mild RI: CrCl>50 to ≤80 mL/min (Group 2)
    • Moderate RI: CrCl>30 to ≤50 mL/min (Group 3)
    • Severe RI: CrCl≤30 mL/min (Group 4)
    • End-stage renal disease (ESRD): CrCl≤30 mL/min, requiring hemodialysis (Group 5)
    • T2DM and severe RI: CrCl≤30 mL/min (Group 6)
  • Age 18 to 80 years
  • BMI 18 to 40 kg/m2, and minimum body mass of at least 45 kg for females
  • 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:

Participants (with or without RI) who met any of the following criteria were not included in this trial:

  • Relevant gastrointestinal tract surgery (except appendectomy, cholecystectomy, or herniotomy)
  • Diseases of the central nervous system, such as epilepsy, seizures, relevant neurological disorders, or psychiatric disorders
  • History of relevant orthostatic hypotension, fainting spells or blackouts; systolic blood pressure <100 or >160 mm Hg, diastolic blood pressure <60 or >100 mm Hg, pulse rate <50 or >100 1/min
  • Chronic or relevant acute infections
  • History of allergy/hypersensitivity (including drug allergies) that were deemed relevant to the trial as judged by the investigator
  • Intake of drugs with a long half-life (>24 h) within at least one month prior to study start, or planned intake of study medication within ≤10 half-lives of administration of another medication. Medications that patients with RI were currently taking for treatment of renal disease were not included under this criterium.
  • Use of medications during the trial or within 10 days prior to administration of study medication that might reasonably influence the results of the trial, based on knowledge at the time of protocol preparation. Co-medications known to inhibit or induce P-glycoprotein or CYP3A were not allowed. Inhibitors of P-glycoprotein or CYP3A include protease inhibitors (such as ritonavir, lopinavir, nelfinavir); azole antimycotics, (itraconazole, ketoconazole, miconazole); macrolide antibiotics, (clarithromycin, erythromycin); amiodarone, cimetidine, diltiazem, fluvoxamine, mibefradil, nefazodone, verapamil, tacrolimus, quinidine, reserpine, and cyclosporine A. Inducers of P-gp or CYP3A include carbamazepine, phenobarbital, phenytoin, rifabutin, rifampin, St. John's Wort and troglitazone. In uncertain cases, a case-by-case decision was made after consultation with the sponsor.
  • Participation in a previous trial with an investigational drug within 2 months of study start if the previous trial was a multiple dose study, or within 1 month of study start if the previous trial was a single dose study
  • Smoker (more than 10 cigarettes or 3 cigars or 3 pipes per day)
  • Inability to refrain from smoking when confined to the study site on trial days
  • Alcohol abuse (more than 60 g/day in males or more than 40 g/day in females)
  • Drug abuse, in the investigator's judgment, based on review of the participant's history and urine screening for abused substances
  • Veins unsuited for intravenous puncture on either arm (e.g. veins which were difficult to locate, access or puncture, veins with a tendency to rupture during or after puncture)
  • Blood donation (more than 100 mL within 4 weeks prior to administration of study medication or during the trial)
  • Excessive physical activities (within 48 h prior to start of the trial or during the trial)
  • Any laboratory value outside the reference range that was of clinical relevance (exceptions were in patients with RI who had abnormal renal function tests or deviations of clinical laboratory values that were related to renal impairment)
  • Inability to comply with the dietary regimen of study centre
  • Inability to understand and comply with protocol requirements, instructions and protocol-stated restrictions

For female patients

  • Pregnancy
  • Positive pregnancy test (human chorionic gonadotropin (β HCG) in urine))
  • No adequate contraception in women of childbearing potential (adequate contraception was considered to be sterilisation, use of an intrauterine device, or use of oral contraception along with a barrier method)
  • Lactation period

Subjects with normal renal function (Group 1) and subjects with T2DM and normal renal function (Group 7) who met the following criterium were not included in this trial:

  • Significant gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders as judged by the investigator

Patients with RI who met any of the following criteria were not included in this trial:

  • Moderate and severe concurrent liver function impairment (for example, due to hepatorenal syndrome)
  • Patients with significant diseases other than renal impairment were excluded. A significant disease was defined as a disease which in the opinion of the investigator put the patient at risk during participation in the study, could influence the results of the study, could influence the patient's ability to participate in the study, or was an unstable condition. Patients with diabetes (for Groups 1 to 5) or hypertension could be included in the trial if the disease was not significant according to these criteria.
  • Haemoglobin <8 g/dL, indicating severe anaemia of renal origin (use of erythropoietin was allowed to maintain haematocrit)

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: Ikke-randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Group 1
Linagliptin in subjects with normal renal function
Eksperimentel: Group 2
Linagliptin in patients with mild renal insufficiency (RI)
Eksperimentel: Group 3
Linagliptin in patients with moderate RI
Eksperimentel: Group 4
Linagliptin in patients with severe RI
Eksperimentel: Group 5
Linagliptin in patients with end-stage renal disease (ESRD)
Eksperimentel: Group 6
Linagliptin in patients with severe RI and Type 2 diabetes mellitus (T2DM)
Eksperimentel: Group 7
Linagliptin in patients with normal renal function and T2DM

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Tidsramme
AUCτ,ss (area under the concentration time curve of the analyte in plasma over the time interval from 0 to 24h after the last dose at steady state) - multiple dose groups
Tidsramme: up to 480 hours
up to 480 hours
Cmax,ss (maximum concentration of the analyte in plasma at steady state) - multiple dose groups
Tidsramme: up to 480 hours
up to 480 hours
AUC0-24 (area under the concentration time curve of the analyte in plasma over the time interval from 0 to 24h after the first dose) - single dose groups
Tidsramme: up to 24 hours
up to 24 hours
Cmax (maximum concentration of the analyte in plasma) - single dose groups
Tidsramme: up to 264 hours
up to 264 hours

Sekundære resultatmål

Resultatmål
Tidsramme
Antal patienter med bivirkninger
Tidsramme: op til 53 dage
op til 53 dage
tmax,(ss) (time from last dosing to maximum concentration of the analyte in plasma after the first dose or at steady state) - multiple dose groups
Tidsramme: up to 480 hours
up to 480 hours
C24,(ss) (concentration of the analyte in plasma at steady state after administration of the first or last dose at the end of the dosing interval) - multiple dose groups
Tidsramme: up to 480 hours
up to 480 hours
λz,(ss) (terminal rate constant in plasma after single dose/at steady state) - multiple dose groups
Tidsramme: up to 480 hours
up to 480 hours
t1/2,(ss) (terminal half-life of the analyte in plasma after single dose/at steady state) - multiple dose groups
Tidsramme: up to 480 hours
up to 480 hours
MRTpo,(ss) (mean residence time of the analyte in the body after single dose/at steady state after oral administration) - multiple dose groups
Tidsramme: up to 480 hours
up to 480 hours
CL/F,(ss) (apparent clearance of the analyte in the plasma after extravascular administration after single dose/at steady state) - multiple dose groups
Tidsramme: up to 480 hours
up to 480 hours
Vz/F,(ss) (apparent volume of distribution during the terminal phase λz after single dose/at steady state following extravascular administration) - multiple dose groups
Tidsramme: up to 480 hours
up to 480 hours
AUC0-∞ (area under the concentration time curve of the analyte in plasma over the time interval from 0 extrapolated to infinity after single dose in severely impaired or end stage renal disease (ESRD) patients)
Tidsramme: up to 264 hours
up to 264 hours
AUC0-tz (area under the concentration-time curve of the analyte in plasma over the time interval from 0 to the time of the last quantifiable data point after single dose in severely impaired or ESRD patients)
Tidsramme: up to 264 hours
up to 264 hours
%AUCtz-∞ (percentage of area under the concentration-time curve of the analyte in plasma over the time interval from the time of the last quantifiable data point extrapolated to infinity after single dose in severely impaired or ESRD patients)
Tidsramme: up to 264 hours
up to 264 hours
Assessment of Plasma protein binding
Tidsramme: predose Day 1
predose Day 1
Model-derived AUCτ,ss in severely impaired or ESRD patients
Tidsramme: up to 264 hours
up to 264 hours
Model-derived Cmax,ss in severely impaired or ESRD patients
Tidsramme: up to 264 hours
up to 264 hours
Change in Dipeptidyl peptidase IV (DPP-4) activity in plasma
Tidsramme: up to 480 hours
up to 480 hours
Number of patients with abnormal findings in physical examination
Tidsramme: up to day 32
up to day 32
Number of patients with clinically significant changes in vital signs
Tidsramme: up to day 32
up to day 32
Number of patients with abnormal changes 12-lead ECG (electrocardiogram)
Tidsramme: up to day 32
up to day 32
Number of patients with abnormal changes in laboratory parameters
Tidsramme: up to day 32
up to day 32
Assessment of tolerability by investigator on a 4-point scale
Tidsramme: up to 480 hours
up to 480 hours
AUC0-24 (area under the concentration time curve of the analyte in plasma over the time interval from 0 to 24h after the first dose) - multiple dose groups
Tidsramme: up to 24 hours
up to 24 hours
Cmax (maximum concentration of the analyte in plasma) - multiple dose groups
Tidsramme: up to 480 hours
up to 480 hours

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

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. april 2008

Primær færdiggørelse (Faktiske)

1. februar 2010

Datoer for studieregistrering

Først indsendt

15. juli 2014

Først indsendt, der opfyldte QC-kriterier

15. juli 2014

Først opslået (Skøn)

16. juli 2014

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

16. juli 2014

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

15. juli 2014

Sidst verificeret

1. juni 2014

Mere information

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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