drugset / Trial / NCT04103905
A Study of MIL62 in Treatment of CD20 Positive B-cell Lymphomas
NaSingle-groupOpen-labelTreatment
Summary
This open-label, multicenter,dose-escalating phase I study was designed to evaluate the safety, tolerability, pharmacokinetics and efficacy of MIL62 in Chinese patients with relapsed/refractory CD20-positive B-cell non-Hodgkin lymphoma(NHL) for whom no treatment of higher priority was available.
Timeline
- Start
- 2017-02-10
- Primary completion
- 2019-05-30
- Completion
- 2020-05-29
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | MIL62 | Monoclonal antibody | 200 mg | Intravenous |
| Subject | MIL62 | Monoclonal antibody | 400 mg | Intravenous |
| Subject | MIL62 | Monoclonal antibody | 800 mg | Intravenous |
| Subject | MIL62 | Monoclonal antibody | 1000 mg | Intravenous |
| Subject | MIL62 | Monoclonal antibody | 1500 mg | Intravenous |