Table 3.
Investigational therapies in the pipeline for dermatomyositis.
Target | Drug | NCT | Phase | Country | Status | Primary Outcome Measures |
---|---|---|---|---|---|---|
JAK inhibitor | Baricitinib | NCT04208464 | Phase 2a | UK | Not yet recruiting | Minimal, moderate, or major clinical response according to the IMACS criteria at 24 weeks |
JAK inhibitor | Baricitinib | NCT04972760 | Phase 3 | France | Not yet recruiting | Moderate improvement based on TIS at 24 weeks without prednisone |
JAK inhibitor | Tofacitinib | NCT04966884 | Open Label | China | Recruiting | Number of responders by total improvement score at 12 months |
Anti-interferon B monoclonal antibody | PF-06823859 | NCT03181893 | Phase 2 | USA | Recruiting | CDASI Activity Score at 12 weeks |
T-cell costimulation blockade | Abatacept | NCT02971683 | Phase 3 | USA | Active, not recruiting | IMACS DOI at 24 weeks |
T-cell costimulation blockade | Abatacept | NCT04946669 | Open label | China | Recruiting | IMACS DOI at 12 weeks |
T-cell costimulation blockade | Abatacept | NCT03215927 | Phase 2 | USA | Recruiting | Forced Vital Capacity (FVC) % Change in 24 weeks |
Complement inhibitor | Ravulizumab | NCT04999020 | Phase 3 | USA | Recruiting | Minimal improvement based on TIS at 26 weeks and 50 weeks |