drugset / Trial / NCT06887738
Study of NM8074 in Patients with Dermatomyositis (DM)
NaSingle-groupOpen-labelTreatment
Summary
This is a Phase II, open-label, multicenter study to evaluate the safety and efficacy of NM8074 administered via intravenous infusion in patients with Dermatomyositis (DM).
Timeline
- Start
- 2026-06
- Primary completion
- 2027-11
- Completion
- 2028-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | RUXOPRUBART | Monoclonal antibody | 20 mg/kg | Intravenous |