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Robert A. Terkeltaub, Daniel E. Furst, Katherine Bennett, Karin A. Kook, R. S. Crockett, and Matthew W. Davis ARTHRITIS & RHEUMATISM Vol. 62, No. 4, April.

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Presentation on theme: "Robert A. Terkeltaub, Daniel E. Furst, Katherine Bennett, Karin A. Kook, R. S. Crockett, and Matthew W. Davis ARTHRITIS & RHEUMATISM Vol. 62, No. 4, April."— Presentation transcript:

1 Robert A. Terkeltaub, Daniel E. Furst, Katherine Bennett, Karin A. Kook, R. S. Crockett, and Matthew W. Davis ARTHRITIS & RHEUMATISM Vol. 62, No. 4, April 2010, pp 1060–1068 High Versus Low Dosing of Oral Colchicine for Early Acute Gout Flare R2 Kim Hyuck / Prof. Son Kyeong Min

2 Introduction Colchicine : mainly used in the treatment and prophylaxis of gout flare –the evidence basis : remarkably limited (Only 1 randomized, placebo-controlled trial,n =43) The AGREE (Acute Gout Flare Receiving Colchicine Evaluation) – study compared low- and high-dose colchicine –randomized, placebo-controlled design. –Pharmacokinetic profiles : comparable maximum blood concentrations (Cmax). –high-dose regimen : 4.8 mg total over 6 hours –low-dose regimen :1.8 mg total over 1 hour

3 Patient and methods Characterization of colchicine pharmacokinetics In healthy volunteers who had fasted –low-dose colchicine :1.2 mg followed by 0.6 mg in 1 hour [1.8 mg total] –high-dose colchicine :1.2 mg followed by 0.6 mg every hour for 6 hours [4.8 mg total] –single-dose colchicine : 0.6 mg

4 Patient and methods6.84 2.5 6.19

5 AGREE study population Male and postmenopausal female patients –>18 years of age with a confirmed past diagnosis of gout total of 575 patients total of 575 patients –randomized to 1 of 3 treatment groups – 1) “low-dose” colchicine, 2) “high-dose” colchicine, 3)placebo

6 Patient and methods AGREE study design Multicenter(54), randomized, double-blind, placebo- controlled, parallel-group, dose comparison between April 2007 and October 2008 The patient : a standardized diary – pain, symptoms, adverse events (AEs), and rescue medication use(e.g. NSAID)

7 Patient and methods AGREE statistical analysis and end points The primary end point : >50% pain reduction at 24 hours without rescue medication (e.g. NSAID) The primary analysis –Comparison of high-dose colchicine and placebo groups –Comparison of low dose colchicine with placebo groups

8 Result Characteristics of the AGREE study subjectsFindings of the AGREE efficacy evaluationFindings of the AGREE safety evaluation

9 Result : Characteristics of the AGREE study subjects. AGREE (Acute Gout Flare Receiving Colchicine Evaluation) patient flow diagram

10 Result : Characteristics of the AGREE study subjects. Baseline characteristics of the patients

11 Result : Findings of the AGREE efficacy evaluation Efficacy analysis

12 Result : Findings of the AGREE efficacy evaluation Distribution of percent improvement

13 Result : Findings of the AGREE safety evaluation Incidence of most frequent adverse events

14 ConclusionEfficacySafty low-dose colchicine High-dose colchicine low-dose colchicine High-dose colchicine


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