drugset / Trial / NCT05074550
Safety Evaluation Study for Patients With Polycythemia Vera
NaSequentialOpen-labelTreatment
Summary
This is PhaseI Dose-Escalation Study to Evaluate the Safety and Pharmacokinetics of PPMX-T003 in Polycythemia Vera
Timeline
- Start
- 2022-08-24
- Primary completion
- 2023-08-01
- Completion
- 2024-03-31
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | PPMX-T003 | Monoclonal antibody | 0.25 mg/kg | Intravenous |
| Subject | PPMX-T003 | Monoclonal antibody | 0.4 mg/kg | Intravenous |
| Subject | PPMX-T003 | Monoclonal antibody | 0.64 mg/kg | Intravenous |
| Subject | PPMX-T003 | Monoclonal antibody | 1 mg/kg | Intravenous |