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Strive to enable biopharmaceuticals created and manufactured by China to benefit patients worldwide |
At present, 3SBio products that are registered overseas include YISAIPU, TPIAO, EPIAO, Intefen and SEPO, etc. The registration has covered nearly 40 countries and regions around the world, with the business and customer scope basically covering all the developing countries. After years of hard work, these products have also been registered and listed in many countries.
In the future, 3SBio’s international business will focus on emerging markets or developing countries such as Brazil, Mexico, Colombia in Latin America, Indonesia, Philippines, Thailand in Southeast Asia, Russia, Ukraine, Uzbekistan in CIS, Turkey, Saudi Arabia, Egypt, Jordan, Morocco in Middle East and North Africa, India, Sri Lanka, Pakistan and Bangladesh in South Asia. It will promote the overseas distribution of EPO, TPO, Yisaipu and SEPO via out-licensing or partnerships with local agents. At the same time, the Company will actively participate in the development of overseas pharmaceutical industries and contribute to the improvement of medical capabilities in developing countries through technology transfers, local joint ventures, capital contribution with technologies, and mergers and acquisitions.
Published at the 74th Annual Scientific Meeting of the American College of Rheumatology (ACR), Atlanta, Georgia, USA, in November 10, 2010.
Abstract 1811. In the “real life” environment, the 20-week efficacy and safety analysis was conducted in the 110 patients who received Etanar® (25 mg, subcutaneous injection, twice a week) in combination with multiple DMARD anti-RA treatment for a long time.
This article was published as a poster in EULARL 2015 (Rome, Italy) (P. Santos-Moreno et al. Ann Rheum Dis 2015; 74:789-790).
The descriptive cross-sectional study included 158 RA patients who visited at least 6 rheumatologists within the past 24 months, and respectively received adalimumab (61 (38.6%), infliximab (35 (22.2 %) and YISAIPU biosimilar products (62 (39.2%) (Etanar® CP Guojian Pharmaceutical Co., Ltd. (China)).
(PISantos-Moreno, G. Sánchez, D. Gómez, C. Castro. Clinical and Experimental Rheumatology, 2015; 33: 858-862.) A multicenter observational cohort study evaluated the clinical reactions at the 12th month in 105 RA patients treated with Etanar (rhTNFR:Fc) and the incidence of the adverse reactions was recorded.
(Pedro Santos-Moreno, Guillermo Sánchez, Danny Gómez. et al; JCR-Journal of Clinical Rheumatology, 2016; 22 (2):57-62) The observational retrospective cohort study compared the clinical reactions at 36 months after treatment in 307 RA patients who received YISAIPU (Etanar®), infliximab (Remecade®) or adalimumab (Humira®) and evaluated the adverse events.
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