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Camrelizumab Utilization on Patients With Advanced Liver Cancer

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Xi'an Jiaotong University

Status

Enrolling

Conditions

Advanced Hepatocellular Carcinoma

Treatments

Other: camrelizumab

Study type

Interventional

Funder types

Other

Identifiers

NCT04487704
XJYFY-KRLZ-HCC-1

Details and patient eligibility

About

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

Full 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;

Enrollment

1,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 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

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

1,000 participants in 1 patient group

Camrelizumab in the treatment of liver cancer
Other group
Description:
Camrelizumab intravenous infusion (no need for prophylactic administration), no less than 30 min
Treatment:
Other: camrelizumab

Trial contacts and locations

1

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Central trial contact

Xu-Feng Zhang, MD,phD; Rui Qu

Data sourced from clinicaltrials.gov

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