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Polymerized-type I collagen for the treatment of patients with rheumatoid arthritis. Effect of intramuscular administration in a double blind placebo-controlled clinical trial
J. Furuzawa-Carballeda, R. Fenutria-Ausmequet, V. Gil-Espinosa, F. Lozano-Soto, M.A. Teliz-Meneses, C. Romero-Trejo, J. Alcocer-Varela
CER2888
2006 Vol.24, N°5
PI 0514, PF 0520
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PMID: 17181919 [PubMed]
Abstract
OBJECTIVES:
To determine the efficacy, tolerance and safety of intramuscular injections of porcine type I collagen-PVP in patients with RA in a long term-therapy.
METHODS:
The study was a double blind placebo-controlled and included 30 patients with active RA (ACR). Patients were treated with intramuscular injections of 2 ml of collagen-PVP (3.4 mg of collagen) or 2 ml of placebo during 6 months. The follow up was done during the next 6 months. The primary endpoints included the Ritchie index (RI), swollen joint count, disease activity score (DAS), erythrocyte sedimentation rate (ESR), and C-reactive protein (CRP). The secondary endpoints included morning stiffness, pain intensity on a visual analogue scale (VAS), and Spanish-health assessment questionnaire (HAQ-DI). Improvement was determined using American College of Rheumatology response criteria (ACR20, 50 and 70).
RESULTS:
Collagen-PVP was safe and well tolerated. There were no adverse events. Patients had a statistically significant improvement (p < 0.05) in collagen-PVP-treated vs. placebo at 6 months of treatment in: swollen joint count (7.1 ± 0.8 vs. 16.0 ± 1.6), RI (8.1 ± 0.8 vs. 15.2 ± 1.5), morning stiffness (9.2 ± 3.1 vs. 29.1 ± 5.9 min), HAQ-DI (50.0 ± 10.8 vs. 22.9 ± 10.3), DAS (3.0 ± 0.2 vs. 4.9 ± 0.3), ACR20 (78.6 vs. 71.4%), ACR50 (57.1 vs. 0%) and ACR70 (7.1 vs. 0%) and CRP (1.1 ± 0.4 vs. 2.5 ± 0.7). Patients treated with collagen-PVP required lower doses of methotrexate vs. placebo (12.6 ± 0.6 vs. 14.2 ± 0.7 at 6 months and 12.3 ± 0.8 vs. 15.4 ± 0.6 at 12 months; p < 0.05). Serological or haematological parameters remained unchanged.
CONCLUSIONS:
Collagen-PVP has been shown to be a safe and well-tolerated drug for the long-term treatment of RA. Combination of collagen-PVP plus methotrexate was more efficacious than methotrexate alone. This biodrug can be useful in the treatment of RA.