drugset / Trial / NCT01129648

Study to Evaluate sUA-Lowering Activity, Safety & PK Interaction of Oral BCX4208 & Allopurinol Admin. in Subjects w/Gout

NCT01129648

Phase 2 Completed 87 enrolled BioCryst Pharmaceuticals
RandomizedFactorialQuadruple-blindTreatment

Summary

To evaluate safety and efficacy of BCX4208 alone and in combination with allopurinol in subjects with gout.

Timeline

Start
2010-05
Primary completion
2010-11
Completion
2010-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Allopurinol Small molecule 100 mg
Subject Allopurinol Small molecule 200 mg
Subject Allopurinol Small molecule 300 mg
Subject Ulodesine Small molecule 20 mg
Subject Ulodesine Small molecule 40 mg
Subject Ulodesine Small molecule 80 mg

Indications