drugset / Trial / NCT00525213

Study to Evaluate the Efficacy and Safety of Orally Administered Rob 803 When Added to Methotrexate

NCT00525213 ↗

Phase 2 Completed 224 enrolled OxyPharma
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of this study is to evaluate the efficacy (ACR20) of Rob 803 administered orally once daily for 12 weeks in combination with a stable dose of methotrexate in subjects with moderate or severe active RA.

Timeline

Start
2007-10
Primary completion
2009-08
Completion
2009-08

Drugs

EvaluationDrugModalityDoseRoute
Comparator Rob 803 Unknown — Oral

Indications