RecruitingPhase 1NCT04794972

A Study of GNC-039, a Tetra-specific Antibody, in Participants With Relapsed/Refractory or Metastatic Solid Tumors

An Open-Label, Multi-Center, Phase I Study to Evaluate the Safety, Tolerability,Pharmacokinetic/Pharmacodynamics and Anti-tumor Activity of Tetra-specific Antibody GNC-039 in Participants With Relapsed/Refractory or Metastatic Solid Tumors


Sponsor

Sichuan Baili Pharmaceutical Co., Ltd.

Enrollment

60 participants

Start Date

Apr 14, 2021

Study Type

INTERVENTIONAL

Conditions

Summary

In this study, the safety, tolerability and preliminary effectiveness of GNC-039 in patients with relapsed/refractory or metastatic glioma or other solid tumors 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-039.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called GNC-039 for people with recurrent glioma and solid tumor. The study is currently recruiting participants at 6 locations. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGGNC-039

Administration by intravenous infusion.


Locations(6)

Beijing Tiantan Hospital, Capital Medical University

Beijing, Beijing Municipality, China

Affiliated Cancer Hospital of Chongqing Medical University

Chongqing, Chongqing Municipality, China

ZhuJiang Hospital of Southern Medical University

Guangzhou, Guangdong, China

Shenzhen Second People's Hospital

Shenzhen, Guangdong, China

The First Affiliated Hospital of Xi'an Jiao Tong University

Xian, Shanxi, China

West China Hospital,Sichuan University

Chengdu, Sichuan, China

View Full Details on ClinicalTrials.gov

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NCT04794972


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