drugset / Trial / NCT05338957
A Study of MRG002 in the Treatment of Patients With HER2-expressed Advanced Malignant Solid Tumors.
NaSingle-groupOpen-labelTreatment
Summary
The objective of this study is to assess the safety and tolerability of MRG002 in combination with HX008 in patients with HER2-expressed advanced malignant solid tumors; and to , explore the maximum tolerated dose (MTD), and to determine the recommended phase II dose (RP2D) of combination therapy; , and to evaluate the preliminary efficacy, pharmacokinetics, and immunogenicity of combination therapy in the targeted study population.
Timeline
- Start
- 2022-08-05
- Primary completion
- 2024-06
- Completion
- 2024-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Pucotenlimab | Monoclonal antibody | 3 mg/kg | Intravenous |
| Subject | TRASTUZUMAB VEDOTIN | Unknown | 1.8 mg/kg | Intravenous |
| Subject | TRASTUZUMAB VEDOTIN | Unknown | 2.2 mg/kg | Intravenous |
| Subject | TRASTUZUMAB VEDOTIN | Unknown | 2.6 mg/kg | Intravenous |