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- Ensayo clínico NCT02191228
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
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
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Actual)
Fase
- Fase 1
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
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 de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: No aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Group 1
Linagliptin in subjects with normal renal function
|
|
|
Experimental: Group 2
Linagliptin in patients with mild renal insufficiency (RI)
|
|
|
Experimental: Group 3
Linagliptin in patients with moderate RI
|
|
|
Experimental: Group 4
Linagliptin in patients with severe RI
|
|
|
Experimental: Group 5
Linagliptin in patients with end-stage renal disease (ESRD)
|
|
|
Experimental: Group 6
Linagliptin in patients with severe RI and Type 2 diabetes mellitus (T2DM)
|
|
|
Experimental: Group 7
Linagliptin in patients with normal renal function and T2DM
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Periodo de tiempo |
|---|---|
|
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
Periodo de tiempo: up to 480 hours
|
up to 480 hours
|
|
Cmax,ss (maximum concentration of the analyte in plasma at steady state) - multiple dose groups
Periodo de tiempo: 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
Periodo de tiempo: up to 24 hours
|
up to 24 hours
|
|
Cmax (maximum concentration of the analyte in plasma) - single dose groups
Periodo de tiempo: up to 264 hours
|
up to 264 hours
|
Medidas de resultado secundarias
Medida de resultado |
Periodo de tiempo |
|---|---|
|
Número de pacientes con eventos adversos
Periodo de tiempo: hasta 53 días
|
hasta 53 días
|
|
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
Periodo de tiempo: 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
Periodo de tiempo: up to 480 hours
|
up to 480 hours
|
|
λz,(ss) (terminal rate constant in plasma after single dose/at steady state) - multiple dose groups
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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)
Periodo de tiempo: 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)
Periodo de tiempo: 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)
Periodo de tiempo: up to 264 hours
|
up to 264 hours
|
|
Assessment of Plasma protein binding
Periodo de tiempo: predose Day 1
|
predose Day 1
|
|
Model-derived AUCτ,ss in severely impaired or ESRD patients
Periodo de tiempo: up to 264 hours
|
up to 264 hours
|
|
Model-derived Cmax,ss in severely impaired or ESRD patients
Periodo de tiempo: up to 264 hours
|
up to 264 hours
|
|
Change in Dipeptidyl peptidase IV (DPP-4) activity in plasma
Periodo de tiempo: up to 480 hours
|
up to 480 hours
|
|
Number of patients with abnormal findings in physical examination
Periodo de tiempo: up to day 32
|
up to day 32
|
|
Number of patients with clinically significant changes in vital signs
Periodo de tiempo: up to day 32
|
up to day 32
|
|
Number of patients with abnormal changes 12-lead ECG (electrocardiogram)
Periodo de tiempo: up to day 32
|
up to day 32
|
|
Number of patients with abnormal changes in laboratory parameters
Periodo de tiempo: up to day 32
|
up to day 32
|
|
Assessment of tolerability by investigator on a 4-point scale
Periodo de tiempo: 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
Periodo de tiempo: up to 24 hours
|
up to 24 hours
|
|
Cmax (maximum concentration of the analyte in plasma) - multiple dose groups
Periodo de tiempo: up to 480 hours
|
up to 480 hours
|
Colaboradores e Investigadores
Patrocinador
Publicaciones y enlaces útiles
Enlaces Útiles
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
- Enfermedades Renales
- Enfermedades urológicas
- Insuficiencia renal
- Agentes hipoglucemiantes
- Efectos fisiológicos de las drogas
- Mecanismos moleculares de acción farmacológica
- Inhibidores de enzimas
- Hormonas
- Hormonas, sustitutos hormonales y antagonistas hormonales
- Inhibidores de la proteasa
- Incretinas
- Inhibidores de la dipeptidil-peptidasa IV
- Linagliptina
Otros números de identificación del estudio
- 1218.26
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