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OpenTrials
Completed

NCT Number: NCT03465059

Safety and Pharmacokinetics of Zanubrutinib (BGB-3111) in Healthy Subjects and Those With Impaired Liver Function

This study is designed to evaluate the safety and pharmacokinetics of zanubrutinib in subjects with impaired liver function in comparison with healthy subjects

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

University of Miami, Miami, Florida, United States

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male and/or female subjects in good health as determined by past medical history, physical examination, vital signs, ECG and laboratory tests at screening.
  • Subjects must have a body mass index (BMI) between 18 and 40 kg/m2 to participate at screening.
  • Female subject must be of non-childbearing potential, i.e. surgically sterile at least 6 months prior to screening with supportive clinical documentation OR post-menopausal must have no regular menstrual bleeding for at least 12 months prior to inclusion. Menopause will be confirmed by a plasma FSH level of >40 IU/L
  • Male subjects must agree to practice 2 highly effective methods of birth control at least one method must be barrier technique.

Additional Inclusion Criteria for Healthy Subjects Only:

  • In good health as determined by past medical history, physical examination, vital signs, ECG, and laboratory tests at screening; subjects without diseases/conditions
  • Matched with a hepatic impaired patient (mild, moderate or severe, as applicable) using the following criteria: sex, age ±10 years and body mass index (BMI)± 10 kilograms

Additional Inclusion Criteria for Hepatic Impaired Subjects Only:

  • History of cirrhosis with supportive documentation (ultrasonography, computed tomography scan, liver biopsy, magnetic resonance imaging, clinical laboratory tests results or physical signs consistent with a clinical diagnosis of liver cirrhosis.
  • Child-Pugh Clinical Assessment Score consistent with degree of hepatic impairment.
  • Blood pressure of 90 to 155 mmHg (systolic) and 50 to 100 mmHg (diastolic).
  • Otherwise considered healthy in general as determined by physical examination findings and laboratory assessments within normal limits.

Exclusion criteria

  • Subjects with a clinically relevant history or presence of any clinically significant disease.
  • History of drug or alcohol abuse within the 12 months prior to dosing.
  • A positive human immunodeficiency virus (HIV) Type 1 or 2 test result at screening.
  • History of blood donation of 500 mL or more of blood within 2 months prior to screening
  • A positive tuberculosis test result.

Additional Exclusion Criteria for Hepatic Impaired Subjects Only:

  • Received a liver transplant
  • Acute or exacerbating hepatitis
  • Active Stage 3 or 4 hepatic encephalopathy
  • Previously diagnosed with hepatocellular carcinoma, or a history of cholestatic liver disease or biliary sepsis within the past 2 years.
  • Additional Exclusion Criteria for Healthy Subjects Only: A positive Hepatitis B surface antigen (HBsAg) or Hepatitis C test result.
  • History of any clinically significant chronic and/or active hepatic disease.

Treatment and study plan

Zanubrutinib

Drug

A single oral dose of 80 mg Zanubrutinib will be administered.

Primary outcomes

  1. Plasma concentration of Zanubrutinib (BGB-3111) to evaluate protocol specified PK parameters

    Time frame: Days 1, 2 & 3

    Plasma concentration of Zanubrutinib (BGB-3111) to evaluate Area Under the Plasma Concentration-Time Curve (AUC) of Zanubrutinib

  2. Plasma concentration of Zanubrutinib (BGB-3111) to evaluate protocol specified PK parameters

    Time frame: Days 1, 2 & 3

    Plasma concentration of Zanubrutinib (BGB-3111) to evaluate Maximum Observed Plasma Concentration (Cmax) of Zanubrutinib

Secondary outcomes

  1. Treatment-Emergent Adverse Events (AE)

    Time frame: up to Day 17

    Percentage of Participants with Treatment-Emergent Adverse Events (AE)

Sponsors and collaborators

Lead sponsor

BeiGene

Industry

Registry information

Official study title

A Phase 1, Open-label, Single-dose Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Zanubrutinib (BGB-3111) in Subjects With Varying Degrees of Hepatic Impairment

Important dates

Study start
2018
Primary completion
2018
Study completion
2018
First posted
Mar 14, 2018
Registry last updated
Apr 24, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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