CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 51 enrolled
Drug / intervention
CRx-102 (2.7/180) +4 moredrug
Likely dose
CRx-102 (2.7/180) 2.7 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00551707
NCT00551707Phase 2Completed

A Randomized, Double-Blind, Placebo-Controlled, Multi-Center Study to Evaluate the Superiority of CRx-102 Over Each of Its Components When Given to Subjects With Active Rheumatoid Arthritis (RA)

Zalicus·interventional·Posted Oct 31, 2007·Updated Apr 29, 2014

In Brief

A Phase 2 clinical trial evaluating CRx-102 (2.7/180), prednisolone, and 3 other interventions for Rheumatoid Arthritis. Completed, enrolled 51 participants across 48 sites in 12 countries.

Detailed Summary

CRx-102 is a synergistic combination drug candidate containing the cardiovascular drug dipyridamole and a very low dose of the glucocorticoid prednisolone. CRx-102 is believed to work through a novel mechanism of action in which dipyridamole selectively amplifies the anti-inflammatory and immunomodulatory activities of the glucocorticoid without replicating the dose-dependent adverse effects. CRx-102 has been associated with clinical benefit in proof of concept studies in subjects with hand Osteoarthritis (OA) and Rheumatoid Arthritis (RA). In this trial, CRx-102 will be given to subjects with active RA as an add-on therapy to existing stable doses of Disease Modifying Anti-Rheumatic Drugs (DMARDs) including methotrexate (MTX), sulfasalazine, hydroxychloroquine, leflunomide or azathioprine. MTX in combination with other DMARDs (e.g., sulfasalazine or hydroxychloroquine) will be permitted to reflect the current standard of care practices within rheumatology.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesArgentina, Canada, Estonia, Hungary, Lithuania, Mexico, Poland, Romania, Russia, Serbia, South Africa, United States
Collaborators--

Timeline

Phase 2CompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedOct 31, 2007
Enrollment StartOct 1, 2007
Primary CompletionNov 1, 2008
Study CompletionJan 1, 2009
TodayJul 2, 2026
Enrollment to primary: 1.1 yearsPosted 18.7 years ago

Interventions

CRx-102 (2.7/180)drug

prednisolone 2.7 mg plus dipyridamole 180 mg

prednisolonedrug

prednisolone (2.7 mg)

dipyridamoledrug

dipyridamole 360 mg

placebodrug

placebo

CRx-102 (2.7/360)drug

Prednisolone 2.7 mg plus Dipyridamole 360 mg