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Chemo-immunotherapy for Cervical Cancer Stage IIICp Trial

W

Women's Hospital School Of Medicine Zhejiang University

Status and phase

Enrolling
Phase 2

Conditions

Immunochemotherapy
Cervical Cancer

Treatments

Drug: Camrelizumab combined with chemotherapy

Study type

Interventional

Funder types

Other

Identifiers

NCT07167160
IRB-20250023

Details and patient eligibility

About

Efficacy evaluation of camrelizumab combined with chemotherapy for adjuvant treatment of patients with pathologically confirmed lymph node-positive cervical cancer after staging surgery.

Enrollment

59 estimated patients

Sex

Female

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients with cervical cancer staged FIGO2018 IIIC1p or IIIC2p after radical surgery;
  2. Positive PD-L1 expression;
  3. ECOG score ≤1

Exclusion criteria

  1. Positive parametrium or surgical margin;
  2. Incomplete radical surgery;
  3. Residual target lesions;
  4. Active autoimmune disease or autoimmune disease requiring systemic treatment;
  5. Previous treatment with immune checkpoint inhibitors.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

59 participants in 1 patient group

chemotherapy group
Experimental group
Treatment:
Drug: Camrelizumab combined with chemotherapy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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