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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
51
Isis Investigational site
Kamloops, British Columbia, Canada
Isis Investigational Site
Toronto, Ontario, Canada
Isis Investigational Site
Montreal, Quebec, Canada
Isis Investigational Site
Safety
Adverse events, laboratory tests, and vital signs
Time frame: 155 Days
hsCRP
The effects of treatment with ISIS CRP Rx or Placebo on hsCRP
Time frame: 155 Days
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Moscow, Russia
Isis Investigational Site
Moscow, Russia
Isis Investigational Site
Moscow, Russia
Isis Investigational Site
Saint Petersburg, Russia
Isis Investigational Site
Saint Petersburg, Russia
Isis Investigational Site
Saint Petersburg, Russia
Isis Investigational Site
Saint Petersburg, Russia