Camrelizumab Utilization on Patients With Advanced Liver Cancer

  • STATUS
    Recruiting
  • End date
    Jan 13, 2025
  • participants needed
    1000
  • sponsor
    First Affiliated Hospital Xi'an Jiaotong University
Updated on 13 May 2022

Summary

To observe and evaluate the safety and efficacy of camrelizumab in advanced liver cancer

Description

camrelizumab , a humanized monoclonal antibody against PD-1, has been shown to block the binding of PD-1 to PD-L1, thereby inhibiting the immune escape of tumor cells. It has a high affinity for PD-1 (KD = 3.31 nmol/L), a high acceptor proportion (85% at 200 mg) of circulating T lymphocytes, and binds to epitopes different from Nivolumab and pembrolizumab,Phase 1 clinical trials have shown that camrelizumab is well tolerated and has antitumor activity in patients with advanced solid tumors.camrelizumab has been approved for indication for advanced hepatocellular carcinoma The main objective of this study was to observe and evaluate the safety and efficacy of treatment regiments containing Camrelizumab in advanced liver cancer。 The subjects included people over 18 years old, For men and women with advanced liver cancer confirmed by histopathology or cytology;

Details
Condition Advanced Hepatocellular Carcinoma
Treatment Camrelizumab
Clinical Study IdentifierNCT04487704
SponsorFirst Affiliated Hospital Xi'an Jiaotong University
Last Modified on13 May 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

years old or more
For both men and women
Patients with advanced liver cancer confirmed by histopathology or cytology; .Volunteer to join the study, sign the informed consent, good compliance, and cooperate with the follow-up

Exclusion Criteria

A known allergy to the study drug or any of its excipients; Or had a severe allergic reaction to other monoclonal antibodies
Patients who are ready for or have previously received an organ or allogeneic bone marrow transplant
Pregnant or lactating women
According to the judgment of the researcher, the patients should not be included in this study
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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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