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A real world clinical study of carilizumab in the treatment of primary liver cancer

A real-world clinical study of Camrelizumb in the treatment of primary liver cancer

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000034264
Enrollment
Unknown
Registered
2020-06-30
Start date
2020-06-30
Completion date
Unknown
Last updated
2020-07-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Primary liver cancer

Interventions

single arm:Camrelizumb

Sponsors

The Second Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. There are no gender limits for patients over 18 years old; 2. Subjects with primary liver cancer confirmed by histopathology or cytology or in accordance with the clinical diagnostic criteria in the diagnostic and therapeutic criteria for primary liver cancer (2019 Edition); 3. Subjects with measurable target lesions examined by CT or MRI, except those with adjuvant therapy; 4. Subjects with child Pugh score <= 9; 5. ECoG physical status score was 0 ~ 2 points; 6. Patients who voluntarily join the study, sign informed consent, have good compliance and cooperate with follow-up; 7. The researchers believe that treatment can benefit.

Exclusion criteria

Exclusion criteria: 1. Patients who have been proved to be allergic to the test drug and its excipients; 2. Patients with active immunodeficiency disease or history of organ transplantation; 3. Patients with heart clinical symptoms or diseases that are not well controlled, for example: (1) NYHA grade 2 and above heart failure (2) Unstable angina pectoris (3) Myocardial infarction occurred within 1 year; 4. Patients with previous and current history of pulmonary fibrosis, interstitial pneumonia and severe impairment of lung function; 5. Pregnant or lactating women; 6. According to the judgment of the researcher, the patients who are not suitable to be included in this study.

Design outcomes

Primary

MeasureTime frame
mPFS;RFS;

Secondary

MeasureTime frame
Adverse events;ORR;DCR;DoR;OS;

Countries

China

Contacts

Public ContactZhendong Chen

The Second Affiliated Hospital of Anhui Medical University

ay2chenzhendong@163.com+86 13805519892

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 14, 2026