MQX-503, a novel formulation of nitroglycerin, improves the severity of Raynaud's phenomenon

Lorinda Chung, Lee Shapiro, David Fiorentino, Murray Baron, Joseph Shanahan, Sangeeta Sule, Vivien Hsu, Naomi Rothfield, Virginia Steen, Richard W. Martin, Edwin Smith, Maureen Mayes, Robert Simms, Janet Pope, Bashar Kahaleh, M. E. Csuka, Barry Gruber, David Collier, Nadera Sweiss, Adam GilbertFrederick J. Dechow, Jeffrey Gregory, Fredrick M. Wigley

Research output: Contribution to journalArticlepeer-review

Abstract

Objective. Raynaud's phenomenon (RP) affects 3-9% of the general population and >90% of patients with systemic sclerosis. Nitrates are often prescribed for the treatment of RP, but currently available formulations are limited by side effects, particularly headaches, dizziness, and skin irritation. The purpose of this study was to evaluate the tolerability and efficacy of a novel formulation of topical nitroglycerin, MQX-503, in the treatment of RP in an ambulatory setting. Methods. We conducted a multicenter, randomized, placebo-controlled study with a 2-week single-blind run-in period to determine baseline severity, followed by a 4-week double-blind treatment phase. Two hundred nineteen adult patients with a clinical diagnosis of primary or secondary RP received 0.9% MQX-503 gel or matching placebo during the treatment period. Gel was applied immediately before or within 5 minutes of the beginning of an episode of RP (maximum of 4 applications daily). End points included the change in the mean Raynaud's Condition Score (RCS; scale 0-10), the frequency and duration of episodes, and subjective assessments at the target week (the week during the treatment phase that most closely matched the run-in period in terms of ambient temperature) compared with baseline. Results. The mean (%) change in the RCS at the target week compared with baseline was significantly greater in the MQX-503 group (0.48 [14.3%]) than that in the placebo group (0.04 [1.3%]; P = 0.04). Changes in the frequency and duration of RP episodes and subjective assessments were not statistically different between the groups. MQX-503 had a side effect profile similar to that of placebo. Conclusion. MQX-503 is well tolerated and more effective than placebo for the treatment of RP.

Original languageEnglish (US)
Pages (from-to)870-877
Number of pages8
JournalArthritis and rheumatism
Volume60
Issue number3
DOIs
StatePublished - Mar 2009

ASJC Scopus subject areas

  • Immunology and Allergy
  • Rheumatology
  • Immunology
  • Pharmacology (medical)

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