drugset / Trial / NCT01414101

Safety, Tolerability, and Pharmacodynamic Study of ISIS CRP Rx in Rheumatoid Arthritis

NCT01414101 ↗

Phase 2 Completed 51 enrolled Ionis Pharmaceuticals, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics of ISIS CRP Rx and its effects on CRP and other pharmacodynamic measures, versus placebo, in subjects with active rheumatoid arthritis.

Timeline

Start
2011-08
Primary completion
2013-05
Completion
2013-05

Drugs

EvaluationDrugModalityDoseRoute
Subject ISIS CRP Rx Antisense oligonucleotide 100 mg Subcutaneous
Subject ISIS CRP Rx Antisense oligonucleotide 200 mg Subcutaneous
Subject ISIS CRP Rx Antisense oligonucleotide 400 mg Subcutaneous

Indications