Ezt az oldalt automatikusan lefordították, és a fordítás pontossága nem garantált. Kérjük, olvassa el a angol verzió forrásszöveghez.

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

2014. október 17. frissítette: 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.

A tanulmány áttekintése

Állapot

Befejezve

Körülmények

Beavatkozás / kezelés

Tanulmány típusa

Beavatkozó

Beiratkozás (Tényleges)

40

Fázis

  • 1. fázis

Kapcsolatok és helyek

Ez a rész a vizsgálatot végzők elérhetőségeit, valamint a vizsgálat lefolytatásának helyére vonatkozó információkat tartalmazza.

Tanulmányi helyek

      • Cologne, Németország
        • 1
      • Rendsburg, Németország
        • 2

Részvételi kritériumok

A kutatók olyan embereket keresnek, akik megfelelnek egy bizonyos leírásnak, az úgynevezett jogosultsági kritériumoknak. Néhány példa ezekre a kritériumokra a személy általános egészségi állapota vagy a korábbi kezelések.

Jogosultsági kritériumok

Tanulmányozható életkorok

18 év (Felnőtt, Idősebb felnőtt)

Egészséges önkénteseket fogad

Igen

Tanulmányozható nemek

Összes

Leírás

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

Tanulási terv

Ez a rész a vizsgálati terv részleteit tartalmazza, beleértve a vizsgálat megtervezését és a vizsgálat mérését.

Hogyan készül a tanulmány?

Tervezési részletek

  • Kiosztás: Nem véletlenszerű
  • Beavatkozó modell: Párhuzamos hozzárendelés
  • Maszkolás: Nincs (Open Label)

Fegyverek és beavatkozások

Résztvevő csoport / kar
Beavatkozás / kezelés
Kísérleti: Group 1: Healthy subjects
Single dose of 100 mg Lacosamide
Single dose of 100 mg Lacosamide tablet
Más nevek:
  • Vimpat
Kísérleti: Group 2: Subjects with mild renal insufficiency
Single dose of 100 mg Lacosamide
Single dose of 100 mg Lacosamide tablet
Más nevek:
  • Vimpat
Kísérleti: Group 3: Subjects with moderate renal insufficiency
Single dose of 100 mg Lacosamide
Single dose of 100 mg Lacosamide tablet
Más nevek:
  • Vimpat
Kísérleti: Group 4: Subjects with severe renal insufficiency
Single dose of 100 mg Lacosamide
Single dose of 100 mg Lacosamide tablet
Más nevek:
  • Vimpat
Kísérleti: Group 5: Subjects with end stage renal insufficiency
Single dose of 100 mg Lacosamide
Single dose of 100 mg Lacosamide tablet
Más nevek:
  • Vimpat

Mit mér a tanulmány?

Elsődleges eredményintézkedések

Eredménymérő
Intézkedés leírása
Időkeret
Area under the Lacosamide plasma concentration time curve from 0 to the last quantifiable data point (AUC(0-tz))
Időkeret: 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
Időkeret: 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
Időkeret: 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
Időkeret: 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

Másodlagos eredményintézkedések

Eredménymérő
Intézkedés leírása
Időkeret
Time of observed maximum (tmax) of Lacosamide concentration
Időkeret: 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
Időkeret: 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
Időkeret: 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)
Időkeret: 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
Időkeret: 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))
Időkeret: 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)
Időkeret: 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)
Időkeret: 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)
Időkeret: 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
Időkeret: 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
Időkeret: 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
Időkeret: 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)
Időkeret: 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)
Időkeret: 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)
Időkeret: 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)
Időkeret: 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
Időkeret: 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)
Időkeret: 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
Időkeret: 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)
Időkeret: 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
Időkeret: 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
Időkeret: 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

Együttműködők és nyomozók

Itt találhatja meg a tanulmányban érintett személyeket és szervezeteket.

Publikációk és hasznos linkek

A vizsgálattal kapcsolatos információk beviteléért felelős személy önkéntesen bocsátja rendelkezésre ezeket a kiadványokat. Ezek bármiről szólhatnak, ami a tanulmányhoz kapcsolódik.

Tanulmányi rekorddátumok

Ezek a dátumok nyomon követik a ClinicalTrials.gov webhelyre benyújtott vizsgálati rekordok és összefoglaló eredmények benyújtásának folyamatát. A vizsgálati feljegyzéseket és a jelentett eredményeket a Nemzeti Orvostudományi Könyvtár (NLM) felülvizsgálja, hogy megbizonyosodjon arról, hogy megfelelnek-e az adott minőség-ellenőrzési szabványoknak, mielőtt közzéteszik őket a nyilvános weboldalon.

Tanulmány főbb dátumok

Tanulmány kezdete

2004. június 1.

Elsődleges befejezés (Tényleges)

2004. november 1.

A tanulmány befejezése (Tényleges)

2004. november 1.

Tanulmányi regisztráció dátumai

Először benyújtva

2013. február 19.

Először nyújtották be, amely megfelel a minőségbiztosítási kritériumoknak

2013. február 21.

Első közzététel (Becslés)

2013. február 22.

Tanulmányi rekordok frissítései

Utolsó frissítés közzétéve (Becslés)

2014. október 20.

Az utolsó frissítés elküldve, amely megfelel a minőségbiztosítási kritériumoknak

2014. október 17.

Utolsó ellenőrzés

2013. február 1.

Több információ

Ezt az információt közvetlenül a clinicaltrials.gov webhelyről szereztük be, változtatás nélkül. Ha bármilyen kérése van vizsgálati adatainak módosítására, eltávolítására vagy frissítésére, kérjük, írjon a következő címre: register@clinicaltrials.gov. Amint a változás bevezetésre kerül a clinicaltrials.gov oldalon, ez a webhelyünkön is automatikusan frissül. .

Klinikai vizsgálatok a Egészséges

Klinikai vizsgálatok a Lacosamide tablet

3
Iratkozz fel