drugset / Trial / NCT07409103

A Study to Assess the Safety and Efficacy of Different Doses of ELV001 to Treat Active Rheumatoid Arthritis in Patients With an Inadequate Response to Methotrexate and Tumor Necrosis Factor Inhibition (START SYNERGY)

NCT07409103 ↗

Phase 2 Recruiting 180 enrolled Elevara Medicines Limited
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a Phase 2 randomized, double-blind, placebo-controlled study with a total duration of 32 weeks from Screening to End-of-Study (EOS) Visit. Approximately 180 participants are planned to be enrolled. The number of participants can be extended to maximally 220 to account for dropouts during the study.

Timeline

Start
2026-02-18
Primary completion
2027-04-15
Completion
2028-03-31

Drugs

EvaluationDrugModalityDoseRoute
Subject ELV001 Unknown 25 mg —
Subject ELV001 Unknown 75 mg —
Subject ELV001 Unknown 125 mg —

Indications