drugset / Trial / NCT06226350

A Phase Ⅱ Study of F520 in Patients With Cervical Carcinoma

NCT06226350

Phase 2 Completed 29 enrolled Shandong New Time Pharmaceutical Co., LTD
NaSingle-groupOpen-labelTreatment

Summary

This study was an open, single-arm, enriched, multicenter Phase II study.

Timeline

Start
2021-03-04
Primary completion
2023-12-05
Completion
2024-01-03

Drugs

EvaluationDrugModalityDoseRoute
Subject F520 Monoclonal antibody 3 mg/kg Intravenous

Indications