drugset / Trial / NCT06887738

Study of NM8074 in Patients with Dermatomyositis (DM)

NCT06887738

Phase 2 Not yet recruiting 8 enrolled NovelMed Therapeutics
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

EvaluationDrugModalityDoseRoute
Subject RUXOPRUBART Monoclonal antibody 20 mg/kg Intravenous

Indications