Clinical Trials Directory

Trials / Active Not Recruiting

Active Not RecruitingNCT05160545

A Study of GNC-035, a Tetra-specific Antibody, in Participants With Locally Advanced or Metastatic Breast Cancer

An Open-Label, Multi-Center, Phase I Study I Study to Evaluate the Safety, Tolerability, Pharmacokinetic/Phamacodynamics and Anti-tumor Activity of Tetra-specific Antibody GNC-035 in Participants With Locally Advanced or Metastatic Breast Cancer

Status
Active Not Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
36 (actual)
Sponsor
Sichuan Baili Pharmaceutical Co., Ltd. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

In this study, the safety, tolerability and preliminary effectiveness of GNC-035 in participants with locally advanced or metastatic Breast Cancer will be investigated to assess the dose-limiting toxicity (DLT), maximum tolerated dose (MTD) or maximum administered dose (MAD) for MTD is not reached of GNC-035.

Conditions

Interventions

TypeNameDescription
DRUGGNC-035Administration by intravenous infusion

Timeline

Start date
2021-11-26
Primary completion
2025-12-01
Completion
2025-12-01
First posted
2021-12-16
Last updated
2025-09-26

Locations

6 sites across 1 country: China

Source: ClinicalTrials.gov record NCT05160545. Inclusion in this directory is not an endorsement.