drugset / Trial / NCT03916094
Evaluate Safety, Tolerability and Pharmacokinetics of HLX22 in Patients With Advanced Solid Tumors Overexpressing HER2
NaSingle-groupOpen-labelTreatment
Summary
a single-center, open-label, dose-escalation Phase I clinical trial to evaluate the safety and the tolerability of HLX22 in patients with advanced solid tumors overexpressing HER2 after failure of standard of care.
Timeline
- Start
- 2019-07-31
- Primary completion
- 2021-01-04
- Completion
- 2021-12-27
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | HLX22 | Monoclonal antibody | 3 mg/kg | Intravenous |
| Subject | HLX22 | Monoclonal antibody | 10 mg/kg | Intravenous |
| Subject | HLX22 | Monoclonal antibody | 25 mg/kg | Intravenous |