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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 oktober 2014 bijgewerkt door: 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.

Studie Overzicht

Toestand

Voltooid

Interventie / Behandeling

Studietype

Ingrijpend

Inschrijving (Werkelijk)

40

Fase

  • Fase 1

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

      • Cologne, Duitsland
        • 1
      • Rendsburg, Duitsland
        • 2

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 70 jaar (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Ja

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

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

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

  • Toewijzing: Niet-gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Group 1: Healthy subjects
Single dose of 100 mg Lacosamide
Single dose of 100 mg Lacosamide tablet
Andere namen:
  • Vimpat
Experimenteel: Group 2: Subjects with mild renal insufficiency
Single dose of 100 mg Lacosamide
Single dose of 100 mg Lacosamide tablet
Andere namen:
  • Vimpat
Experimenteel: Group 3: Subjects with moderate renal insufficiency
Single dose of 100 mg Lacosamide
Single dose of 100 mg Lacosamide tablet
Andere namen:
  • Vimpat
Experimenteel: Group 4: Subjects with severe renal insufficiency
Single dose of 100 mg Lacosamide
Single dose of 100 mg Lacosamide tablet
Andere namen:
  • Vimpat
Experimenteel: Group 5: Subjects with end stage renal insufficiency
Single dose of 100 mg Lacosamide
Single dose of 100 mg Lacosamide tablet
Andere namen:
  • Vimpat

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Area under the Lacosamide plasma concentration time curve from 0 to the last quantifiable data point (AUC(0-tz))
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Time of observed maximum (tmax) of Lacosamide concentration
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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)
Tijdsspanne: 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
Tijdsspanne: 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))
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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
Tijdsspanne: 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)
Tijdsspanne: 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
Tijdsspanne: 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)
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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

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.

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 juni 2004

Primaire voltooiing (Werkelijk)

1 november 2004

Studie voltooiing (Werkelijk)

1 november 2004

Studieregistratiedata

Eerst ingediend

19 februari 2013

Eerst ingediend dat voldeed aan de QC-criteria

21 februari 2013

Eerst geplaatst (Schatting)

22 februari 2013

Updates van studierecords

Laatste update geplaatst (Schatting)

20 oktober 2014

Laatste update ingediend die voldeed aan QC-criteria

17 oktober 2014

Laatst geverifieerd

1 februari 2013

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 .

Klinische onderzoeken op Gezond

Klinische onderzoeken op Lacosamide tablet

3
Abonneren