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Status:

COMPLETED

Pharmacokinetics and Safety of Single Subcutaneous Pasireotide (SOM230) in Subjects With Varying Degrees of Hepatic Function

Lead Sponsor:

Novartis Pharmaceuticals

Conditions:

Hepatic Cirrhosis

Alcoholism

Eligibility:

All Genders

18-75 years

Phase:

PHASE1

Brief Summary

The purpose of this study is to evaluate the effect of varying degrees of hepatic function (Child-Pugh classification) on the pharmacokinetics and safety of pasireotide s.c. in subjects.

Eligibility Criteria

Inclusion

  • Inclusion criteria:
  • Common Inclusion criteria for all subjects:
  • Male or female subjects between 18 and 75 years of age, inclusive.
  • Vital signs at screening and baseline which are within normal ranges.
  • Subjects must have a BMI between 20 kg/m2 and 30 kg/m2.
  • Inclusion Criteria for cohort 1:
  • • Generally healthy subjects as determined by past medical history, physical examination, vital signs, electrocardiogram and standard laboratory tests at screening.
  • Inclusion Criteria for cohort 2-4:
  • Subjects with confirmed cirrhosis by at least one of the following criteria:
  • Histologically by prior liver biopsy showing cirrhosis.
  • Clinically by physical examination, and/or laboratory data, and/or liver imaging, and/or endoscopic findings.
  • Exclusion criteria:
  • Common Exclusion criteria for all subjects:
  • Donation or loss of 400 mL or more of blood within eight weeks prior to dosing.
  • Subjects with additional active malignant disease within the last five years (with the exception of non-melanoma skin cancers that were not metastatic and have been treated curatively).
  • Subjects with abnormal clinical laboratory values (except the clinical laboratory values linked to hepatic dysfunction).
  • Any surgical or medical condition that may interfere with the conduct of the study, may jeopardize the subject in case of participation in the study or may significantly alter the absorption, distribution, metabolism or excretion of drugs.
  • History of immunocompromise, including a positive HIV test result (ELISA and Western blot). A HIV test will not be required; however, previous medical history will be reviewed
  • Female subjects who are pregnant (positive pregnancy test at screening or at baseline) or lactating, or are of childbearing potential and not practicing a medically acceptable method of birth control.
  • Exclusion Criteria for cohort 1:
  • Clinical evidence of liver disease or liver injury as indicated by abnormal liver function tests.
  • A positive Hepatitis B surface antigen (HBsAg) or Hepatitis C test result (antibody positive subjects will be allowed if non-viremic).
  • Exclusion Criteria for cohort 2-4:
  • Symptoms or history of encephalopathy (Stage III or worse) within three months prior to dosing.
  • Clinical evidence of severe ascites. Exclusion criteria
  • Common Exclusion criteria for all subjects:
  • Donation or loss of 400 mL or more of blood within eight weeks prior to dosing.
  • Subjects with additional active malignant disease within the last five years (with the exception of non-melanoma skin cancers that were not metastatic and have been treated curatively).
  • Subjects with abnormal clinical laboratory values (except the clinical laboratory values linked to hepatic dysfunction).
  • Any surgical or medical condition that may interfere with the conduct of the study, may jeopardize the subject in case of participation in the study or may significantly alter the absorption, distribution, metabolism or excretion of drugs.
  • History of immunocompromise, including a positive HIV test result (ELISA and Western blot). A HIV test will not be required; however, previous medical history will be reviewed
  • Female subjects who are pregnant (positive pregnancy test at screening or at baseline) or lactating, or are of childbearing potential and not practicing a medically acceptable method of birth control.
  • Exclusion Criteria for cohort 1:
  • Clinical evidence of liver disease or liver injury as indicated by abnormal liver function tests.
  • A positive Hepatitis B surface antigen (HBsAg) or Hepatitis C test result (antibody positive subjects will be allowed if non-viremic).
  • Exclusion Criteria for cohort 2-4:
  • Symptoms or history of encephalopathy (Stage III or worse) within three months prior to dosing.
  • Clinical evidence of severe ascites.

Exclusion

    Key Trial Info

    Start Date :

    July 1 2008

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    Estimated Enrollment :

    34 Patients enrolled

    Trial Details

    Trial ID

    NCT00698464

    Start Date

    July 1 2008

    Last Update

    December 21 2020

    Active Locations (4)

    Enter a location and click search to find clinical trials sorted by distance.

    Page 1 of 1 (4 locations)

    1

    McGuire Research Institute VAMC

    Richmond, Virginia, United States, 23249

    2

    Universite Catholique de Louvain

    Brussels, Belgium

    3

    Novartis Investigative site

    Berlin, Germany

    4

    Novartis Investigative Site

    George, South Africa