South Korea-based Daewon Pharmaceutical (Daewon) announced that it has launched the teriparatide biosimilar Terrosa.
Daewon launches teriparatide biosimilar in South Korea
Biosimilars/News | Posted 19/06/2020 0 Post your comment
Teriparatide is a recombinant form of parathyroid hormone (PTH). Teriparatide is identical to a portion of human PTH and intermittent use activates osteoblasts more than osteoclasts, which leads to an overall increase in bone. This makes it an effective anabolic, i.e. bone growing, agent. It is therefore used for the treatment of osteoporosis in postmenopausal women and men at high risk for fracture and for glucocorticoid-induced osteoporosis in men and postmenopausal women.
Daewon signed a licensing agreement with Richter-Helm BioTec, which is a joint venture between Hungary-based Gedeon Richter and Germany’s Helm, to sell Terrosa in South Korea in February 2017. Daewon then received marketing approval from South Korea’s drug regulator, the Ministry of Food and Drug Safety (MFDS), for Terrosa in November 2019 [1].
Terrosa is the first biosimilar of teriparatide to be launched in Korea and the first biological marketed by Daewon. According to the company, ‘the treatment has not only proved its effectiveness and safety but also has excellent price competitiveness, which will likely reduce the burden on patients’.
According to Daewon, the local osteoporosis treatment market has one million patients and is worth about Won 200 billion (US$162.5 million). The injection market for osteoporosis treatment is also estimated at Won 70 billion.
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Biosimilars approved in South Korea
Reference
1. GaBI Online - Generics and Biosimilars Initiative. Teriparatide biosimilar Terossa approved in South Korea [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2020 Jun 19]. Available from: www.gabionline.net/Biosimilars/News/Teriparatide-biosimilar-Terossa-approved-in-South-Korea
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