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Completed

NCT Number: NCT04293029

Pharmacokinetics and Safety of SHR0302 in Patients With Hepatic Impairment

Study to Evaluate Pharmacokinetics and Safety of SHR0302 in Patients With Mild, Moderate Hepatic Impairment and Normal Liver Function in Phase I Clinical Study

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Key information

Conditions

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

The First Affiliated Hospital of Jilin University

Changchun, Jilin, China

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

All subjects::

  • Signing the informed consent forms;
  • 18 years to 65 years (inclusive);
  • Body mass index should be between 18 and 30 kg/m2 (inclusive);
  • No medication was used before screening,or stable medication for 4 weeks.

Normal liver function:

  • Clinical laboratory tests during the screening period were normal,or the abnormality has no clinical significance.

Hepatic impaired subjects:

  • Child-Pugh Classification score clinically determined as mild or moderate hepatic impairment.
  • Liver damage due to primary liver disease.

Exclusion criteria

All subjects:

  • Subject known or suspected of being sensitive to the study drugs or its ingredient;

Normal liver function:

  • Previous history of liver function impairment, or physical examination and laboratory examination at screening indicated the presence or possibility of liver function impairment.
  • Hepatitis B surface antigen (HBsAg) positive or Anti-hepatitis C virus (HCV) antibody or hepatitis C core antigen positive within 3 months prior to administration.

Hepatic impaired subjects:

  • Suspected or diagnosed as liver cancer or with other malignant tumors;
  • Drug induced liver injury,acute liver injury,liver transplantation history.
  • Subjects with hepatic failure,or severe complications caused by Hepatocirrhosis.

Treatment and study plan

SHR0302

Drug

SHR0302

Primary outcomes

  1. Peak Plasma Concentration (Cmax)

    Time frame: 72 hours after dosing

    Peak Plasma Concentration (Cmax) will be compared between normal hepatic function patients and mild or moderate hepatic dysfunction patients

  2. Area under the plasma concentration versus time curve from single dosing time extrapolated to infinity(AUC0-∞)

    Time frame: 72 hours after dosing

    Area under the plasma concentration versus time curve from single dosing time extrapolated to infinity(AUC0-∞) will be compared between normal hepatic function patients and mild or moderate hepatic dysfunction patients

  3. Area under the plasma concentration versus time curve from the last time of dosing to the last measurable concentration (AUC0-t)

    Time frame: 72 hours after dosing

    Area under the plasma concentration versus time curve from the last time of dosing to the last measurable concentration (AUC0-t) will be compared between normal hepatic function patients and mild or moderate hepatic dysfunction patients

Secondary outcomes

  1. Adverse events

    Time frame: 72 hours after dosing

    Number of Participants With Adverse Events and Serious Adverse Events

Sponsors and collaborators

Lead sponsor

Jiangsu HengRui Medicine Co., Ltd.

Industry

Registry information

Official study title

Pharmacokinetics and Safety of SHR0302 in Patients With Mild, Moderate Hepatic Impairment and Normal Liver Function in Phase I Clinical Study

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Mar 3, 2020
Registry last updated
Oct 14, 2021

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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