Exploring the Efficacy, Safety and Cost-effectiveness Analysis of Cadonilimab in the Treatment of Cervical Cancer

NCT06140589 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2024-09-19

No results posted yet for this study

Summary

Cadonilimab, a PD-1/CTLA-4 bi-specific antibody, is being developed by Akeso, Inc. for the treatment of a range of solid tumors, including cervical cancer, lung cancer, gastric/gastroesophageal junction cancer, liver cancer and nasopharyngeal cancer. Cadonilimab was approved in China in June 2022 for use in patients with relapsed or metastatic cervical cancer who have progressed on or after platinum-based chemotherapy. The clinicopathological data of patients with persistent, recurrent or metastatic cervical cancer treated with Cadonilimab were collected, and medical images (magnetic resonance, CT, etc.) before and after treatment were followed up, and the efficacy was evaluated according to RECIST standards. The incidence and severity of adverse events and clinically significant abnormal laboratory test results were collected to evaluate the safety of the drug. Survival benefit analysis is conducted based on the patient's survival time and medical expenses.

Conditions

Interventions

DRUG

Cadonilimab

The intravenous dose of Cadonilimab was 10mg/kg, and every 3 weeks was a course of treatment; Or 6mg/kg, every 2 weeks for a course of treatment

Sponsors & Collaborators

  • Fujian Medical University Affiliated Nanping First Hospital

    collaborator UNKNOWN
  • The First Hospital Affiliated to Fujian Medical University

    collaborator UNKNOWN
  • Fujian Medical University Union Hospital

    collaborator OTHER
  • Gutian Hospital

    collaborator UNKNOWN
  • Jiangxi Provincial Cancer Hospital

    collaborator OTHER
  • Shunde Women and Children's Hospital (Maternity and Child Healthcare Hospital of Shunde Foshan)

    collaborator UNKNOWN
  • Lianyungang Donghai County People's Hospital

    collaborator UNKNOWN
  • Changsha Maternal and Child Health Hospital

    collaborator UNKNOWN
  • Pingxiang Maternal and Child Health Hospital

    collaborator UNKNOWN
  • Huinan County People's Hospital

    collaborator UNKNOWN
  • People's Hospital Affiliated to Fujian University of Traditional Chinese Medicine

    collaborator UNKNOWN
  • Fujian Cancer Hospital

    lead OTHER_GOV

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-09-07
Primary Completion
2024-12-31
Completion
2026-12-31

Countries

  • China

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06140589 on ClinicalTrials.gov