BIIB023 Proof-of-Concept Study in Participants With Lupus Nephritis
Stopped early · Phase 2 · Has a placebo group
Conditions studied: Lupus Nephritis
In brief
The primary objective of the study is to assess the efficacy of BIIB023 as an add-on treatment to background therapy compared with placebo in combination with background therapy in the treatment of participants with active, biopsy-proven lupus nephritis. The secondary objectives of this study are to assess the safety and tolerability of BIIB023 compared with placebo in this study population.
Key facts
- Study ID
- NCT01499355
- Run by
- Biogen
- People needed
- 276
- Starts
- 2012-07-01
- Expected to finish
- 2015-12-01
- Last updated by the study team
- 2017-01-18
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Research Site — Orlando, Florida, United States
- Research Site — Boston, Massachusetts, United States
- Research Site — Rochester, Minnesota, United States
- Research Site — Lake Success, New York, United States
- Research Site — Chapel Hill, North Carolina, United States
- Research Site — Columbus, Ohio, United States
- Research Site — Memphis, Tennessee, United States
- Research Site — El Paso, Texas, United States
- Research Site — Capital Federal, Ciudad Autonoma Buenos Aires, Argentina
- Research Site — Córdoba, Córdoba Province, Argentina
- Research Site — San Miguel de Tucumán, Tucumán Province, Argentina
- Research Site — Ciudad Autonoma Buenos Aires, Argentina
- Research Site — La Plata, Argentina
- Research Site — San Juan, Argentina
- Research Site — San Miguel de Tucumán, Argentina
- Research Site — Melbourne, Victoria, Australia
- Research Site — Leuven, Belgium
- Research Site — Liège, Belgium
- Research Site — Cuiabá, Mato Grosso, Brazil
- Research Site — São Paulo, São Paulo, Brazil
- Research Site — Barranquilla, Colombia
- Research Site — Bogotá, Colombia
- Research Site — Medellín, Colombia
- Research Site — Pessac, Gironde, France
- Research Site — Torrance, California, United States
Full record on ClinicalTrials.gov
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