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Amiprilose Hydrochloride for Rheumatoid Arthritis

Wayne G. Riskin, MD; Dennis B. Gillings, PhD; and John A. Scarlett, MD
[+] Article and Author Information

This article was presented in part on 17 June 1989 at the annual meeting of the American College of Rheumatology, Cincinnati, Ohio.

Grant Support: Supported in part by grants from Greenwich Pharmaceuticals Inc.

Requests for Reprints: Wayne G. Riskin, MD, 4700-C Sheridan Street, Hollywood, FL 33021.

Current Author Addresses: Dr. Riskin: 4700-C Sheridan Street, Hollywood, FL 33021.

Dr. Gillings: Quintiles, Inc., 1829 E. Franklin St, Chapel Hill, NC 27514.

Dr. Scarlett: Greenwich Pharmaceuticals, 501 Office Center Drive, Ft. Washington, PA 19034.


© 1989 American College of PhysiciansAmerican College of Physicians


Ann Intern Med. 1989;111(6):455-465. doi:10.7326/0003-4819-111-6-455
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Study Objective: To assess the safety and efficacy of amiprilose hydrochloride (HCl), a novel synthetic carbohydrate with anti-inflammatory and immunomodulatory properties, in patients with rheumatoid arthritis.

Design: Prospective, multicenter, randomized, parallel group, double-blind placebo-controlled 12-week trial.

Patients: Two hundred and one functional class I and II patients with definite or classic rheumatoid arthritis, previously untreated with disease modifying antirheumatic drugs.

Interventions: Patients were withdrawn from nonsteroidal anti-inflammatory drug therapy. Those who flared were randomly assigned to amiprilose HCl, 6 g/d, or placebo for 12 weeks. No concomitant anti-inflammatory or antirheumatic drug therapy was permitted during the study. Combination acetaminophen and propoxyphene napsylate was the only supplemental analgesic medication allowed.

Measurements and Main Results: The number of painful joints and swollen joints, joint pain and joint swelling indices, left and right grip strength, investigator global assessment, and patient global assessment returned to baseline for the amiprilose group and showed statistically significant (P < 0.05) differences from the placebo group within 4 to 6 weeks. The protocol criteria for overall therapeutic response were satisfied by 41% of the amiprilose patients, compared with 21% of the placebo group (P = 0.003). Approximately 0.5 tablet per day less analgesic medication was taken by the amiprilose group (P < 0.05 at weeks 6 and 12). There were no statistically significant differences in morning stiffness, walking time, erythrocyte sedimentation rate, C-reactive protein, or rheumatoid factor between the groups. A similar number of adverse experiences were reported by the patients on amiprilose (67%) and on placebo (63%). One patient on amiprilose developed thrombocytopenia of unknown cause; no other reported adverse effects were serious.

Conclusions: Amiprilose HCl has significant anti-inflammatory activity and a favorable safety profile when used as the sole antirheumatic therapy in patients with active rheumatoid arthritis. Synthetic carbohydrates may represent an important new class of drugs for the treatment of inflammatory, autoimmune diseases.

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