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A Study to Assess the Effect of Severe Hepatic Impairment on the Pharmacokinetics of Intravenous Conivaptan

30 avril 2014 mis à jour par: Cumberland Pharmaceuticals

A Phase 1, Open-Label Study to Assess the Effect of Severe Hepatic Impairment on the Pharmacokinetics of Intravenous Conivaptan

The purpose of this study is to assess the pharmacokinetics and safety of a 48-hour continuous infusion of conivaptan in subjects with severe liver impairment compared to subjects with normal liver function.

Aperçu de l'étude

Statut

Complété

Les conditions

Intervention / Traitement

Description détaillée

Subjects will be admitted to the Phase 1 unit Day -2 and will remain confined to the unit until discharge on Study Day 5 after completion of all study procedures.

Type d'étude

Interventionnel

Inscription (Réel)

17

Phase

  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

    • California
      • Anaheim, California, États-Unis, 92801
        • Advanced Clinical Research Institute
    • Colorado
      • Lakewood, Colorado, États-Unis, 80228
        • DaVita Clinical Research
    • Florida
      • Orlando, Florida, États-Unis, 32809
        • Orlando Clinical Research

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

30 ans à 75 ans (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

Subjects with Normal Hepatic Function:

Female subject must be either:

  • post-menopausal prior to Screening, or
  • premenarchal prior to Screening, or
  • documented surgically sterile or post hysterectomy, or
  • if of childbearing potential, must have a negative pregnancy test at Screening and must be using highly effective contraception prior to Screening and throughout the study period and for 28 days after final study drug administration

    • Female subject must not be lactating and must not be breastfeeding at Screening or during the study period, and for 28 days after final study drug administration
    • Female subject must not donate ova starting at Screening or during the study period, and for 28 days after final study drug administration
    • Male subject must:
  • be using highly effective contraception consisting of two forms of birth control (one of which must be a barrier method) starting at Screening and continue throughout the study period, and for 28 days after final study drug administration
  • not donate sperm starting at Screening and throughout the study period, and for at least 28 days after final study drug administration

    • Subject weighs at least 45 kg and has a body mass index between 18 and 40 kg/m2 inclusive
    • The subject must have clinical laboratory test results within normal range, including liver function tests (LFTs)
    • The subject must have had a normal 12-lead electrocardiogram (ECG)

Hepatic Impaired Subjects:

  • Female subject must be either:

    • post-menopausal prior to Screening, or
    • premenarchal prior to Screening, or
    • documented surgically sterile or post hysterectomy, or
    • if of childbearing potential, must have a negative pregnancy test at Screening and must be using highly effective contraception prior to Screening and throughout the study period and for 28 days after final study drug administration
  • Female subject must not be lactating and must not be breastfeeding at Screening or during the study period, and for 28 days after final study drug administration
  • Female subject must not donate ova starting at Screening or during the study period, and for 28 days after final study drug administration
  • Male subject must:

    • be using highly effective contraception consisting of two forms of birth control (one of which must be a barrier method) starting at Screening and continue throughout the study period, and for 28 days after final study drug administration
    • not donate sperm starting at Screening and throughout the study period, and for at least 28 days after final study drug administration
  • Subject meets criteria for severe hepatic impairment defined by Child-Pugh method
  • Subject weighs at least 45 kg and has a body mass index between 18 and 40 kg/m2 inclusive
  • The subject must have clinical laboratory test results within therapeutic range except for hepatic disease
  • The subject must have had a normal 12-lead electrocardiogram (ECG)

Exclusion Criteria:

Subjects with Normal Hepatic Function:

  • Subject has a history of a clinically significant illness, and associated clinical symptoms, medical condition, or laboratory abnormality within past 3 months that would preclude participation in the study
  • Subject has evidence of biliary obstruction or other causes of hepatic impairment
  • Subject is known to have hepatitis or is a carrier of hepatitis B surface antigen (HBsAg), hepatitis C virus (HCV) antibody, or is known to be HIV positive or has HIV antibodies
  • Subject has an impaired ability to sense thirst
  • Subject has serum sodium less than 115mEg/L or greater than 140 mEg/L
  • Subject has either a systolic blood pressure (BP) of greater than 140 mmHg or a diastolic BP of less than 56 mmHg
  • Subject has taken any prescription or over-the-counter medications except for contraceptives, hormone replacement therapy and occasional acetaminophen, or alternative and complementary medicines within past 14 days
  • Subject has a history of carcinoma, except for basal cell or cutaneous squamous cell carcinoma within past 5 years
  • Subject drinks greater than 14 units of alcohol per week (Note: one unit = 12 ounces of beer, 4 ounces of wine, or 1 ounce of spirits)
  • Subject has a history of substance abuse within past 6 months prior to Screening Visit or the subject tests positive at Screening or clinic admission for alcohol or drugs of abuse
  • Subject is currently participating in another clinical trial or has received an investigational medication within past 30 days
  • Subject is known to have hypersensitivity to conivaptan or its derivatives
  • Subject has had a blood transfusion or donated/lost more than 550ml of blood within past 8 weeks
  • Subject is incapable of being compliant with the protocol

Subjects with Hepatic Impairment:

  • Subject has a history of a clinically significant illness, and associated clinical symptoms, medical condition, or laboratory abnormality within past 3 months that would preclude participation in the study. Subjects with controlled hypertension may be allowed
  • Subject has a condition associated with hepatic disease including; biliary obstruction, or other cause of hepatic impairment not related to parenchymal disorder and/or disease of the liver, fluctuating or rapidly deteriorating hepatic function, biliary liver cirrhosis, history or presence of hepatic encephalopathy greater than Grade 1 within past 3 months or unstable encephalopathy prior to Screening, tense ascites, esophageal/gastric variceal bleeding with past 6 months, server portal hypertension, surgical portal systemic shunt or peritoneal venous shunt, thrombocyte level below 50,000 x 10^9/L and prothrombin time (PT) above 18 seconds
  • Subject is hypovolemic or has evidence of orthostatic hypotension
  • Subject has an impaired ability to sense thirst
  • Subject has serum sodium less than 115mEg/L or greater than 140 mEg/L
  • Subject has either a systolic blood pressure (BP) of greater than 140 mmHg or a diastolic BP of less than 56 mmHg
  • Subject is known to be HIV positive or has HIV antibodies
  • Subject has had a change in dose regimen of medication needed for their underlying medical condition with the past four weeks
  • Subject is currently taking a prohibited medication
  • Subject drinks greater than 14 units of alcohol per week (Note: one unit equals 12 ounces of beer, 4 ounces of wine, or 1 ounce of spirits)
  • Subject has a history of substance abuse within past 6 months prior to Screening Visit or the subject tests positive at Screening or clinic admission for alcohol or drugs of abuse
  • Subject is currently participating in another clinical trial or has received an investigational medication with past 30 days
  • Subject has had a blood transfusion or donated/lost more than 550ml of blood within past 8 weeks
  • Subject is known to have hypersensitivity of conivaptan or its derivatives
  • Subject is incapable of being compliant with the protocol

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

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

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Comparateur actif: Sujets ayant une fonction hépatique normale
Intravenous
Autres noms:
  • YM087
  • Vaprisol
Expérimental: Subjects with severe hepatic impairment
Intravenous
Autres noms:
  • YM087
  • Vaprisol

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Délai
Assess the effect of severe hepatic impairment on the plasma drug concentration of conivaptan through analysis of blood samples
Délai: 5 days
5 days

Collaborateurs et enquêteurs

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

Les enquêteurs

  • Directeur d'études: Art Wheeler, MD, Cumberland Pharmaceuticals, Inc.

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 2011

Achèvement primaire (Réel)

1 février 2014

Achèvement de l'étude (Réel)

1 février 2014

Dates d'inscription aux études

Première soumission

8 juin 2011

Première soumission répondant aux critères de contrôle qualité

8 juin 2011

Première publication (Estimation)

9 juin 2011

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Estimation)

2 mai 2014

Dernière mise à jour soumise répondant aux critères de contrôle qualité

30 avril 2014

Dernière vérification

1 avril 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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