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NCT06226350

A Phase Ⅱ Study of F520 in Patients With Cervical Carcinoma

Completed Phase 2 Last updated 26 January 2024
What this trial tests

Phase 2 trial testing Recombinant Humanized Anti-PD-1 Monoclonal Antibody Injection in Cervical Cancer in 29 participants. Completed in 3 January 2024.

Timeline
4 March 2021
Primary endpoint
5 December 2023
3 January 2024

Quick facts

Lead sponsorShandong New Time Pharmaceutical Co., LTD
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment29
Start date4 March 2021
Primary completion5 December 2023
Estimated completion3 January 2024
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Shandong New Time Pharmaceutical Co., LTD — full company profile →

Who can join

18 and older, female only, with Cervical Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Comprehensive overview of antibody drug-related clinical studies in gynecology: insights from ClinicalTrials.gov.
    Zhou X, Xiao L, Lai F, Chen W, et al · · 2025 · cited 1× · PMID 40417700 · DOI 10.3389/fmed.2025.1521587

Verify or expand the search:

Other trials of Recombinant Humanized Anti-PD-1 Monoclonal Antibody Injection

Trials testing the same drug.

Other recruiting trials for Cervical Cancer

Currently open trials in the same condition.

Other Shandong New Time Pharmaceutical Co., LTD trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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