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DOI 10.1016/j.jep.2016.05.031

Медицинская библиотека · Journal of ethnopharmacology · 2016

Gastrointestinal safety and efficacy of long-term GCSB-5 use in patients with osteoarthritis: A 24-week, multicenter study.

Ha Chul-Won, Park Yong-Beom, Kyung Hee-Soo, Han Chung-Soo, Bae Ki-Cheor, Lim Hong-Chul, Park Sang-Eun, Lee Myung Chul, Won Ye-Yeon, Lee Dong-Chul, Cho Sung-Do, Kim Chang-Wan, Kim Jin-Goo, Kang Joon-Soon, Lee Ju-Hong, Choi Eui-Sung, Seon Jong-Keun, Lee Woo-Suk, Bin Seong-Il

Клиническое исследование IV фазыСравнительное исследованиеСтатьяМногоцентровое исследованиеПеревод в очереди

Аннотация

ETHNOPHARMACOLOGY RELEVANCE: A previous study indicated non-inferiority of GCSB-5 to celecoxib regarding efficacy and safety in treating OA; however, the gastrointestinal (GI) safety data was limited to 12 weeks. Accordingly, a longer term study with a larger number of patients was necessary to establish the GI safety of GCSB-5.

AIM OF STUDY: The primary goal was to determine the safety and efficacy of 24-week use of GCSB-5. The secondary goal was to compare the GI safety data of GCSB-5 with that of the previously reported Celecoxib Long-term Arthritis Safety Study (CLASS).

METHOD: This was a 24-week, multicenter, single-arm phase IV Study for the safety and efficacy of GCSB-5. A total of 761 patients were enrolled and 756 patients received at least one dose of GCSB-5. Among them, 629 patients (82.7%) completed the 24 week follow up. The primary goal was to determine the safety and efficacy of GCSB-5 for 24 weeks. The secondary goal was to compare the GI safety data of GCSB-5 with that of the previously reported Celecoxib Long-term Arthritis Safety Study (CLASS).

RESULTS

The incidence of GI disorders of GCSB-5 was 23.7%. The annual rate of perforation, ulcer obstruction, or bleeding (PUB) incidence was 0.0%. The drop-out rate due to GI disorders following GCSB-5 use was 4.8%. Compared to celecoxib data from CLASS, the incidence of GI disorders (23.7% vs. 31.4%, p<0.001), annual rate of PUB and gastroduodenal ulcers (0.0% vs 2.2%, p=0.004), and drop-out rate due to GI disorders following GCSB-5 use were significantly low (4.8% vs 8.7%, p<0.001). Efficacy was proven by significant improvements in Western Ontario McMaster Questionnaire (WOMAC) scale, Korean Knee Score (KKS), 100-mm pain visual analogue scale (VAS), and physician's global assessments of patient's response to therapy (PGART).

CONCLUSIONS

The safety and efficacy profile of GCSB-5 are comparable to celecoxib. These results indicate GCSB-5 is safe for a long-term treatment of knee OA patients.

TRIAL REGISTRATION: ClinicalTrials.gov (NCT01604239).

Для цитирования: Ha Chul-Won, Park Yong-Beom, Kyung Hee-Soo, Han Chung-Soo, Bae Ki-Cheor, Lim Hong-Chul, Park Sang-Eun, Lee Myung Chul, Won Ye-Yeon, Lee Dong-Chul, Cho Sung-Do, Kim Chang-Wan, Kim Jin-Goo, Kang Joon-Soon, Lee Ju-Hong, Choi Eui-Sung, Seon Jong-Keun, Lee Woo-Suk, Bin Seong-Il. Gastrointestinal safety and efficacy of long-term GCSB-5 use in patients with osteoarthritis: A 24-week, multicenter study.. Journal of ethnopharmacology. 2016. DOI: 10.1016/j.jep.2016.05.031.

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