Skip to content

The efficacy and safety of Camrelizumab in treating advanced gynecological tumors

The efficacy and safety of Camrelizumab in treating advanced gynecological tumors

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100049393
Enrollment
Unknown
Registered
2021-08-01
Start date
2021-08-30
Completion date
Unknown
Last updated
2022-04-19

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

Conditions

Gynecologic Oncology

Interventions

Case series:Nil

Sponsors

The First Affiliated Hospital of He'nan University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Female aged >=18 years old, weight>30Kg; 2.Patients with advanced cervical cancer, endometrial cancer, ovarian cancer and other gynecological tumors diagnosed by histology or cytology; 3.At least one measurable lesion (spiral CT scan length of measurable lesion >=10mm or short diameter of enlarged lymph node >=15mm according to RECIST1.1); 4.The researchers determined that patients could receive Carrerizumab; 5.The patient was voluntarily treated with Carrelizumab; 6.Volunteer to join this study, sign informed consent, good compliance and cooperate with follow-up.

Exclusion criteria

Exclusion criteria: 1.Pregnant or nursing women; 2.People allergic to Carrelizumab and its accessories; 3.Patients currently participating in other clinical studies; 4.The researchers judged other circumstances not suitable for inclusion in the study.

Design outcomes

Primary

MeasureTime frame
overall survival;

Secondary

MeasureTime frame
progression free survival;time to progression;objective remission rate;disease control rate;

Countries

China

Contacts

Public ContactWang Yan

The First Affiliated Hospital of He'nan University of Science and Technology

wangyan650727@163.com+86 13700815027

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026