drugset / Trial / NCT04934514
Clinical Study of IAH0968 in Patients With HER2-positive Advanced Solid Tumors
Non-randomizedSequentialOpen-labelTreatment
Summary
This is a phase I/IIa study to evaluate the safety, tolerability and preliminary efficacy of IAH0968 in patients with HER2-positive advanced solid tumors who have failed standard treatment.
Timeline
- Start
- 2021-07-06
- Primary completion
- 2024-12-31
- Completion
- 2025-03-31
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | IAH0968 | Monoclonal antibody | 6 mg/kg | — |
| Subject | IAH0968 | Monoclonal antibody | 10 mg/kg | — |
| Subject | IAH0968 | Monoclonal antibody | 15 mg/kg | — |
| Subject | IAH0968 | Monoclonal antibody | 20 mg/kg | — |
| Background | Cisplatin | Other / unclassified | 75 mg/m2 | Intravenous |
| Background | Gemcitabine | Small molecule | 1000 mg/m2 | Intravenous |