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Study to Evaluate the Pharmacokinetics, Safety, Tolerability of Single Dose Lacosamide in Subjects With Renal Impairment Compared to Healthy Subjects

17 października 2014 zaktualizowane przez: UCB BIOSCIENCES GmbH

Open, Non-randomized, Sequential Group Comparison to Investigate the Pharmacokinetics, Safety, and Tolerability of 100 mg SPM 927 in Male and Female Subjects With Renal Impairment Including Subjects Requiring Dialysis Compared With Male and Female Healthy Subjects Following Single-dose Administration

To investigate the Pharmacokinetics (PK) of oral administered Lacosamide in renal impaired subjects and healthy subjects.

Przegląd badań

Status

Zakończony

Interwencja / Leczenie

Typ studiów

Interwencyjne

Zapisy (Rzeczywisty)

40

Faza

  • Faza 1

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

      • Cologne, Niemcy
        • 1
      • Rendsburg, Niemcy
        • 2

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

18 lat do 70 lat (Dorosły, Starszy dorosły)

Akceptuje zdrowych ochotników

Tak

Płeć kwalifikująca się do nauki

Wszystko

Opis

Inclusion Criteria:

  • Subject was informed and given ample time and opportunity to think about his/her participation and had given his/her written informed consent
  • Subject was willing and able to comply with all trial requirements
  • Subject was a male or female Caucasian, between 18 and 70 years of age (inclusive)
  • If female, subject was of non-childbearing potential (post-menopausal or hysterectomized) or was using medically adequate contraception
  • If female of childbearing potential, subject had a negative pregnancy test
  • Subject had a Body Mass Index (BMI) between 20 and 34 kg/m2 (inclusive)
  • Subject was healthy without clinically relevant cardiovascular, renal, gastrointestinal, hepatic, metabolic, endocrine, neurological, or psychiatric abnormalities detected during Eligibility Assessment (EA)

Subjects with renal impairment also had to fulfill the following inclusion criteria:

  • Subject had no clinically relevant cardiovascular or endocrine findings during EA
  • Subject had a renal impairment. The subjects were assigned to 1 of the following treatment groups according to Creatinine Clearance (CLCr) values determined 2 to 7 days prior to dosing:
  • Group 2: 80 mL/min > CLCr ≥ 50 mL/min (subjects with mild renal impairment)
  • Group 3: 50 mL/min > CLCr ≥ 30 mL/min (subjects with moderate renal impairment)
  • Group 4: CLCr < 30 mL/min (subjects with severe renal impairment, not on dialysis between 2 weeks before EA and end of the trial)

Inclusion criteria for Group 5:

  • Subject was informed and given ample time and opportunity to think about his/her participation and had given his/her written informed consent
  • Subject was willing and able to comply with all trial requirements
  • Subject was a male or female Caucasian, between 18 and 70 years of age (inclusive)
  • If female, subject was of non-childbearing potential (post-menopausal or hysterectomized) or was using medically adequate contraception
  • If female of childbearing potential, subject had a negative pregnancy test
  • Subject had a BMI between 20 and 34 kg/m2 (inclusive)
  • Subject had no clinically relevant cardiovascular or endocrine findings during EA
  • Subject had an endstage renal disease (CLCr < 15 mL/min, determined approximately 2 to 7 days before first dosing) treated with extracorporal hemodialysis for at least 4 months

Exclusion Criteria:

Healthy subjects:

  • Subject had previously participated in this trial
  • Subject had participated in another trial of an investigational product within the last 3 months or was currently participating in another trial of an investigational product
  • Subject had donated blood or had a comparable blood loss (> 500 mL) within the last 3 months prior to EA
  • Subject smoked more than 5 cigarettes per day or had done so within the 6 months prior to commencement of this trial
  • Subject had a history of chronic alcohol or drug abuse within the last 6 months prior to commencement of this trial
  • Subject consumed more than 40 g of alcohol/day (amount corresponds to 1 L beer/day or 0.5 L wine/day or 120 mL liquor/day)
  • Subject had positive tests for alcohol (urine or breath test) or drugs (urine test)
  • Subject had clinically relevant changes in the electrocardiogram (ECG), such as second- or third-degree atrioventricular (AV) block, prolongation of the QRS complex over 120 ms or of the corrected QT (QTc) interval > 430 ms (male subjects) or > 450 ms (female subjects)
  • Subject had a history or present condition of clinically relevant respiratory or cardiovascular disorders, eg, cardiac insufficiency, coronary heart disease, hypertension, arrhythmia, tachyarrhythmia, or status after myocardial infarction
  • Subject had a history or present condition of psychic abnormality, psychiatric or neurologic illness, or autonomic neuropathy that, in the opinion of the Investigator, could have jeopardized or would have compromised the subject's ability to participate in the trial
  • Subject had a history or present condition of seizure disorder
  • Subject had a history or present condition of malignancy
  • Subject had a history or present condition of renal disorders (albuminuria, chronic infections) or renal impairment
  • Subject had a history or present condition of Diabetes Mellitus or thyroid dysfunction, especially Hyperthyreosis, or other endocrine disorders
  • Subject had a clinically relevant allergy
  • Subject had a known or suspected drug hypersensitivity, in particular to the trial medication
  • Subject was taking any concomitant medication currently or within 2 weeks prior to the first day of dosing (with the exception of oral contraceptives and Paracetamol [maximum allowed dose: 1000 mg/dose], which were allowed up to 48 hours prior to dosing); further exceptions could be made if the Investigator and the sponsor jointly considered the medication as acceptable
  • Subject was tested positive for human immunodeficiency virus 1/2 antibodies (HIV-1/2-Ab), hepatitis B surface antigen (HBs-Ag), or hepatitis C virus antibody (HCV-Ab)
  • Subject had any clinically relevant abnormality in the physical examination or in vital sign measurements (systolic blood pressure > 150 mmHg or < 100 mmHg, diastolic blood pressure > 95 mmHg or < 60 mmHg, pulse rate > 100 beats per minute (bpm) or < 50 bpm)
  • Subject had a clinically relevant deviation from the norm in the clinical chemistry, hematology, or urinalysis evaluations

Exclusion criteria for Groups 2-4:

  • Exclusion criteria 1 to 12 for healthy subjects also applied to subjects with renal impairment
  • Subject had a clinically relevant allergy
  • Subject had a known or suspected drug hypersensitivity, in particular to the trial medication
  • Subject was taking any concomitant medication currently or within 2 weeks prior to dosing that could have interfered with the investigational product
  • Subject was tested positive for HIV-1/2-Ab, HBs-Ag, or HCV-Ab
  • Subject had any clinically relevant abnormality in the physical examination or in vital sign measurements (systolic blood pressure > 180 mmHg or < 100 mmHg, diastolic blood pressure > 110 mmHg, pulse rate > 100 bpm or < 60 bpm)
  • Subject had a clinically relevant deviation from the norm in the clinical chemistry, hematology or urinalysis evaluations other than expected for a subject with renal impairment, eg, hemoglobin < 8.0 g/dL

Exclusion criteria for Group 5:

  • Exclusion criteria 1 to 12 for healthy subjects also applied to subjects in Group 5
  • Subject had a clinically relevant allergy
  • Subject had a known or suspected drug hypersensitivity, in particular to the trial medication
  • Subject was tested positive for HIV-1/2-Ab, HBs-Ag, or HCV-Ab
  • Subject was taking any concomitant medication that might interfere with the investigational product currently or within 2 weeks prior to dosing
  • Subject had any clinically relevant abnormality in the physical examination or in vital sign measurements (systolic blood pressure > 200 mmHg [predialysis value] or < 100 mmHg, diastolic blood pressure > 110 mmHg, pulse rate > 100 bpm or < 60 bpm)
  • Subject had a clinically relevant deviation from the norm in the clinical chemistry, hematology, or urinalysis evaluations other than expected for a patient with renal impairment, eg, hemoglobin < 8.0 g/dL

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Przydział: Nielosowe
  • Model interwencyjny: Przydział równoległy
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: Group 1: Healthy subjects
Single dose of 100 mg Lacosamide
Single dose of 100 mg Lacosamide tablet
Inne nazwy:
  • Wimpat
Eksperymentalny: Group 2: Subjects with mild renal insufficiency
Single dose of 100 mg Lacosamide
Single dose of 100 mg Lacosamide tablet
Inne nazwy:
  • Wimpat
Eksperymentalny: Group 3: Subjects with moderate renal insufficiency
Single dose of 100 mg Lacosamide
Single dose of 100 mg Lacosamide tablet
Inne nazwy:
  • Wimpat
Eksperymentalny: Group 4: Subjects with severe renal insufficiency
Single dose of 100 mg Lacosamide
Single dose of 100 mg Lacosamide tablet
Inne nazwy:
  • Wimpat
Eksperymentalny: Group 5: Subjects with end stage renal insufficiency
Single dose of 100 mg Lacosamide
Single dose of 100 mg Lacosamide tablet
Inne nazwy:
  • Wimpat

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Area under the Lacosamide plasma concentration time curve from 0 to the last quantifiable data point (AUC(0-tz))
Ramy czasowe: Day 1 to Day 5 of study
Blood sampling at 0 (predose), 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 36, 48, 60, 72, 84, and 96 hours after single dose administration; > 24 hours excluded for group 5
Day 1 to Day 5 of study
Measured maximal concentration (Cmax) of Lacosamide
Ramy czasowe: Day 1 to Day 5 of study
Blood sampling at 0 (predose), 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 36, 48, 60, 72, 84, and 96 hours after single dose administration; > 24 hours excluded for group 5
Day 1 to Day 5 of study
Area under the Lacosamide plasma concentration-time curve from 0 to the last quantifiable data point (AUC (0-tz)), normalized by body weight
Ramy czasowe: Day 1 to Day 5 of study
Blood sampling at 0 (predose), 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 36, 48, 60, 72, 84, and 96 hours after single dose administration; > 24 hours excluded for group 5
Day 1 to Day 5 of study
Measured maximal concentration (Cmax, norm) of Lacosamide normalized by body weight
Ramy czasowe: Day 1 to Day 5 of study
Blood sampling at 0 (predose), 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 36, 48, 60, 72, 84, and 96 hours after single dose administration; > 24 hours excluded for group 5
Day 1 to Day 5 of study

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Time of observed maximum (tmax) of Lacosamide concentration
Ramy czasowe: Day 1 to Day 5 of study
Blood sampling at 0 (predose), 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 36, 48, 60, 72, 84, and 96 hours after single dose administration; > 24 hours excluded for group 5
Day 1 to Day 5 of study
Time of observed maximum (tmax) of Lacosamide metabolite (SPM12809) concentration
Ramy czasowe: Day 1 to Day 5 of study
Blood sampling at 0 (predose), 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 36, 48, 60, 72, 84, and 96 hours after single dose administration; > 24 hours excluded for group 5
Day 1 to Day 5 of study
Terminal half-life (t1/2) of Lacosamide
Ramy czasowe: Day 1 to Day 5 of study
Blood sampling at 0 (predose), 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 36, 48, 60, 72, 84, and 96 hours after single dose administration; > 24 hours excluded for group 5
Day 1 to Day 5 of study
Terminal half-life (t1/2) of Lacosamide metabolite (SPM12809)
Ramy czasowe: Day 1 to Day 5 of study
Blood sampling at 0 (predose), 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 36, 48, 60, 72, 84, and 96 hours after single dose administration; > 24 hours excluded for group 5
Day 1 to Day 5 of study
Apparent total clearance (CL/f) of Lacosamide from plasma
Ramy czasowe: Day 1 to Day 5 of study
Blood sampling at 0 (predose), 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 36, 48, 60, 72, 84, and 96 hours after single dose administration; > 24 hours excluded for group 5
Day 1 to Day 5 of study
Area under the lacosamide metabolite (SPM12809) plasma concentration-time curve from 0 to the last quantifiable data point (AUC(0-tz))
Ramy czasowe: Day 1 to Day 5 of study
Blood sampling at 0 (predose), 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 36, 48, 60, 72, 84, and 96 hours after single dose administration; > 24 hours excluded for group 5
Day 1 to Day 5 of study
Amount of Lacosamide excreted in urine from 0 to defined time point (Ae(0-48)) (t=48 hours)
Ramy czasowe: Day 1 to Day 3 of study
Urine sampling predose, 0-4, 4-8, 8-12, 12-24, 24-36, and 36-48 hours postdose
Day 1 to Day 3 of study
Amount of Lacosamide metabolite (SPM12809) excreted in urine from 0 to defined time point (Ae(0-48)) (t=48 hours)
Ramy czasowe: Day 1 to Day 3 of study
Urine sampling predose, 0-4, 4-8, 8-12, 12-24, 24-36, and 36-48 hours postdose
Day 1 to Day 3 of study
Measured maximal concentration (Cmax) of Lacosamide metabolite (SPM12809)
Ramy czasowe: Day 1 to Day 5 of study
Blood sampling at 0 (predose), 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 36, 48, 60, 72, 84, and 96 hours after single dose administration; > 24 hours excluded for group 5
Day 1 to Day 5 of study
Area under the Lacosamide metabolite (SPM12809) plasma concentration time curve from 0 to the last quantifiable data point (AUC(0-tz)), normalized by body weight
Ramy czasowe: Day 1 to Day 5 of study
Blood sampling at 0 (predose), 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 36, 48, 60, 72, 84, and 96 hours after single dose administration; > 24 hours excluded for group 5
Day 1 to Day 5 of study
Measured maximal Lacosamide metabolite (SPM12809) concentration (Cmax,norm), normalized by body weight
Ramy czasowe: Day 1 to Day 5 of study
Blood sampling at 0 (predose), 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 36, 48, 60, 72, 84, and 96 hours after single dose administration; > 24 hours excluded for group 5
Day 1 to Day 5 of study
Terminal half-life (t1/2) of Lacosamide in urine
Ramy czasowe: Day 1 to Day 3 of study
Urine sampling predose, 0-4, 4-8, 8-12, 12-24, 24-36, and 36-48 hours postdose
Day 1 to Day 3 of study
Lacosamide concentration in dialysis inlet line (Cin)
Ramy czasowe: From 4 hours up to 6 hours postdose
Dialysis samples collected 4 hours and 6 hours after administration (1.5 hours and 3.5 hours after start of dialysis)
From 4 hours up to 6 hours postdose
Lacosamide metabolite (SPM12809) concentration in dialysis inlet line (Cin)
Ramy czasowe: From 4 hours up to 6 hours postdose
Dialysis samples collected 4 hours and 6 hours after administration (1.5 hours and 3.5 hours after start of dialysis)
From 4 hours up to 6 hours postdose
Lacosamide concentration in dialysis outlet line (Cout)
Ramy czasowe: From 4 hours up to 6 hours postdose
Dialysis samples collected 4 hours and 6 hours after administration (1.5 hours and 3.5 hours after start of dialysis)
From 4 hours up to 6 hours postdose
Lacosamide metabolite (SPM12809) concentration in dialysis outlet line (Cout)
Ramy czasowe: From 4 hours up to 6 hours postdose
Dialysis samples collected 4 hours and 6 hours after administration (1.5 hours and 3.5 hours after start of dialysis)
From 4 hours up to 6 hours postdose
Extraction rate (E) of Lacosamide
Ramy czasowe: From 4 hours up to 6 hours postdose
Dialysis samples collected 4 hours and 6 hours after administration (1.5 hours and 3.5 hours after start of dialysis)
From 4 hours up to 6 hours postdose
Extraction rate (E) of Lacosamide metabolite (SPM12809)
Ramy czasowe: From 4 hours up to 6 hours postdose
Dialysis samples collected 4 hours and 6 hours after administration (1.5 hours and 3.5 hours after start of dialysis)
From 4 hours up to 6 hours postdose
Dialysis clearance (CLdial) of Lacosamide
Ramy czasowe: From 4 hours up to 6 hours postdose
Dialysis samples collected 4 hours and 6 hours after administration (1.5 hours and 3.5 hours after start of dialysis)
From 4 hours up to 6 hours postdose
Dialysis clearance (CLdial) of Lacosamide metabolite (SPM12809)
Ramy czasowe: From 4 hours up to 6 hours postdose
Dialysis samples collected 4 hours and 6 hours after administration (1.5 hours and 3.5 hours after start of dialysis)
From 4 hours up to 6 hours postdose
Rate constant of Lacosamide elimination
Ramy czasowe: Day 1 to Day 5 of study
Blood sampling at 0 (predose), 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 36, 48, 60, 72, 84, and 96 hours after single dose administration; > 24 hours excluded for group 5
Day 1 to Day 5 of study
Rate constant of Lacosamide metabolite (SPM12809) elimination
Ramy czasowe: Day 1 to Day 5 of study
Blood sampling at 0 (predose), 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 36, 48, 60, 72, 84, and 96 hours after single dose administration; > 24 hours excluded for group 5
Day 1 to Day 5 of study

Współpracownicy i badacze

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Publikacje i pomocne linki

Osoba odpowiedzialna za wprowadzenie informacji o badaniu dobrowolnie udostępnia te publikacje. Mogą one dotyczyć wszystkiego, co jest związane z badaniem.

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów

1 czerwca 2004

Zakończenie podstawowe (Rzeczywisty)

1 listopada 2004

Ukończenie studiów (Rzeczywisty)

1 listopada 2004

Daty rejestracji na studia

Pierwszy przesłany

19 lutego 2013

Pierwszy przesłany, który spełnia kryteria kontroli jakości

21 lutego 2013

Pierwszy wysłany (Oszacować)

22 lutego 2013

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Oszacować)

20 października 2014

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

17 października 2014

Ostatnia weryfikacja

1 lutego 2013

Więcej informacji

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

Badania kliniczne na Lacosamide tablet

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