drugset / Trial / NCT06800157

Study of LW402 Tablets in Moderate to Severe Rheumatoid Arthritis

NCT06800157 ↗

Phase 2 Completed 72 enrolled Shanghai Longwood Biopharmaceuticals Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This Phase IIa study is designed to evaluate the dose-response relationship, efficacy, safety, and tolerability of LW402 tablets administered for 12 weeks in adult patients with active rheumatoid arthritis receiving background methotrexate (MTX) therapy.

Timeline

Start
2023-02-27
Primary completion
2024-05-26
Completion
2024-08-30

Drugs

EvaluationDrugModalityDoseRoute
Subject LW402 Unknown 50 mg Oral
Subject LW402 Unknown 125 mg Oral
Background Methotrexate Small molecule — —

Indications