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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 juillet 2014 mis à jour par: 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)

Aperçu de l'étude

Type d'étude

Interventionnel

Inscription (Réel)

51

Phase

  • La phase 1

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans à 80 ans (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Tout

La description

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)

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Non randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Group 1
Linagliptin in subjects with normal renal function
Expérimental: Group 2
Linagliptin in patients with mild renal insufficiency (RI)
Expérimental: Group 3
Linagliptin in patients with moderate RI
Expérimental: Group 4
Linagliptin in patients with severe RI
Expérimental: Group 5
Linagliptin in patients with end-stage renal disease (ESRD)
Expérimental: Group 6
Linagliptin in patients with severe RI and Type 2 diabetes mellitus (T2DM)
Expérimental: Group 7
Linagliptin in patients with normal renal function and T2DM

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Délai
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
Délai: up to 480 hours
up to 480 hours
Cmax,ss (maximum concentration of the analyte in plasma at steady state) - multiple dose groups
Délai: 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
Délai: up to 24 hours
up to 24 hours
Cmax (maximum concentration of the analyte in plasma) - single dose groups
Délai: up to 264 hours
up to 264 hours

Mesures de résultats secondaires

Mesure des résultats
Délai
Nombre de patients présentant des événements indésirables
Délai: jusqu'à 53 jours
jusqu'à 53 jours
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
Délai: 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
Délai: up to 480 hours
up to 480 hours
λz,(ss) (terminal rate constant in plasma after single dose/at steady state) - multiple dose groups
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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)
Délai: 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)
Délai: 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)
Délai: up to 264 hours
up to 264 hours
Assessment of Plasma protein binding
Délai: predose Day 1
predose Day 1
Model-derived AUCτ,ss in severely impaired or ESRD patients
Délai: up to 264 hours
up to 264 hours
Model-derived Cmax,ss in severely impaired or ESRD patients
Délai: up to 264 hours
up to 264 hours
Change in Dipeptidyl peptidase IV (DPP-4) activity in plasma
Délai: up to 480 hours
up to 480 hours
Number of patients with abnormal findings in physical examination
Délai: up to day 32
up to day 32
Number of patients with clinically significant changes in vital signs
Délai: up to day 32
up to day 32
Number of patients with abnormal changes 12-lead ECG (electrocardiogram)
Délai: up to day 32
up to day 32
Number of patients with abnormal changes in laboratory parameters
Délai: up to day 32
up to day 32
Assessment of tolerability by investigator on a 4-point scale
Délai: 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
Délai: up to 24 hours
up to 24 hours
Cmax (maximum concentration of the analyte in plasma) - multiple dose groups
Délai: up to 480 hours
up to 480 hours

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Liens utiles

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude

1 avril 2008

Achèvement primaire (Réel)

1 février 2010

Dates d'inscription aux études

Première soumission

15 juillet 2014

Première soumission répondant aux critères de contrôle qualité

15 juillet 2014

Première publication (Estimation)

16 juillet 2014

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Estimation)

16 juillet 2014

Dernière mise à jour soumise répondant aux critères de contrôle qualité

15 juillet 2014

Dernière vérification

1 juin 2014

Plus d'information

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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