drugset / 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
NaSingle-groupOpen-labelTreatment
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.
Timeline
- Start
- 2021-10-11
- Primary completion
- 2023-08-18
- Completion
- 2023-08-18
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | HLX26 | Monoclonal antibody | 60 mg | Intravenous |
| Subject | HLX26 | Monoclonal antibody | 150 mg | Intravenous |
| Subject | HLX26 | Monoclonal antibody | 300 mg | Intravenous |
| Subject | HLX26 | Monoclonal antibody | 500 mg | Intravenous |
| Subject | HLX26 | Monoclonal antibody | 800 mg | Intravenous |
| Subject | HLX26 | Monoclonal antibody | 1200 mg | Intravenous |
| Subject | HLX26 | Monoclonal antibody | 1600 mg | Intravenous |