RecruitingPhase 1NCT07473726

A Phase I Clinical Study to Evaluate the Safety, Tolerability, and PK of HLX48 in Advanced/Metastatic Solid Tumors

A Phase I Clinical Study to Evaluate the Safety, Tolerability, and Pharmacokinetic Characteristics of HLX48 (EGFR/c-MET Bispecific Antibody-Drug Conjugate) in Participants With Advanced/Metastatic Solid Tumors


Sponsor

Shanghai Henlius Biotech

Enrollment

72 participants

Start Date

Jun 30, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This study is an open-label first-in-human phase I clinical study to evaluate the safety, tolerability, and pharmacokinetic characteristics of HLX48 in patients with advanced/metastatic solid tumors.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called HLX48 for people with advanced/metastatic solid tumors. The study is currently recruiting participants at 7 locations. People eligible for this study include aged 18 Years to 75 Years.

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

DRUGHLX48

EGFR/c-MET Bispecific Antibody-Drug Conjugate


Locations(7)

Macquarie University

North Ryde, New South Wales, Australia

GenesisCare St.Leonards

Saint Leonards, New South Wales, Australia

Peninsula and South Eastern Haematology and Oncology Group

Frankston, Victoria, Australia

Zhujiang Hospital of Southern Medical University

Guangzhou, Guangdong, China

Sun Yat-Sen University Cancer Center

Guangzhou, Guangzhou, China

Shanghai General Hospital

Hongkou, Shanghai Municipality, China

Shanxi Provincial Cancer Hospital

Taiyuan, Shanxi, China

View Full Details on ClinicalTrials.gov

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NCT07473726


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