drugset / Trial / NCT05606263

Efficacy and Safety of Caldonirimab Plus Nimotuzumab for Recurrent or Metastatic Cervical Cancer

NCT05606263

Phase 2 Unknown 55 enrolled Xi'an Jiaotong University
NaSingle-groupOpen-labelTreatment

Summary

To evaluated the efficacy and safety of caldonirimab plus nimotuzumab as second-line or later therapy for recurrent or metastatic cervical cancer

Timeline

Start
2022-11-01
Primary completion
2023-11-30
Completion
2025-11-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Caldonirimab Monoclonal antibody 6 mg/kg
Subject Nimotuzumab Monoclonal antibody 400 mg Intravenous

Indications