OncRef

Clinical Trial: NCT05078593

A Clinical Study to Evaluate the Safety, Tolerability and Pharmacokinetic Characteristics of HLX26 Monoclonal Antibody Injection in Patients With Solid Tumor or Lymphoma

Status:

COMPLETED

Phase:

Phase 1

Lead Sponsor:Shanghai Henlius Biotech
Information Provided By:Shanghai Henlius Biotech
Last Update Posted:2024-02-23

Study Overview

Brief Summary

This study is a first-in-class open-label phase I human clinical study to evaluate the safety and tolerability of HLX26 with escalated doses in the treatment of patients with advanced/metastatic solid tumors or lymphomas.

Official Title

A Phase 1 Clinical Study to Evaluate the Safety, Tolerability and Pharmacokinetic Characteristics of HLX26 Monoclonal Antibody Injection (Anti LAG-3 Monoclonal Antibody) in Patients With Advanced/Metastatic Solid Tumor or Lymphoma

Conditions

Solid Tumor, Adult, Lymphoma

Intervention / Treatment

  • Drug: HLX26

Other Study ID Numbers

  • HLX26-001

Start Date (Actual)

2021-10-11

Primary Completion Date (Actual)

2023-08-18

Study Completion Date (Actual)

2023-08-18

Enrollment (Actual)

18

Study Type

Interventional

Phase

Phase 1