Japanese drug makers Kissei Pharmaceutical Company and JCR Pharmaceuticals have announced positive results of a phase 3 study for JR-131, a proposed biosimilar to darbepoetin alfa (Aranesp).
Japanese drug makers Kissei Pharmaceutical Company and JCR Pharmaceuticals have announced positive results of a phase 3 study for JR-131, a proposed biosimilar to darbepoetin alfa (Aranesp).
Darbepoetin alfa is a long-acting erythropoiesis-stimulating agent for the treatment of renal anemia in people with chronic kidney failure. The therapy is also used to treat anemia caused by chemotherapy in people with certain types of cancer.
The phase 3 study began in August 2016. In the study’s primary efficacy endpoint, JR-131 demonstrated equivalence for variations in hemoglobin concentration and similarity with regard to the 2 products’ safety profiles was confirmed.
Amgen, the maker of the originator product, received FDA approval for Aranesp in 2001, and in 2016, the company reported $526 million in sales of the drug.
Certain drug manufacturers have already launched biosimilars of darbepoetin alfa in less highly regulated territories; companies such as Hetero Drugs, Dr. Reddy’s Laboratories, and Torrent Pharmaceuticals have all launched darbepoetin alfa biosimilars in India, some as early as 2010.
Kissei and JCR entered into a collaborative research and development agreement for JR-131 in September 2013, and aim to apply for marketing approval later in 2018.
The drug makers’ efforts are part over an overall uptick in the Japanese market, which some analysts predict will continue throughout 2018. According to a recent report from CPhI Japan, demographic pressures are increasing healthcare costs, making cost-saving options an appealing investment. As a result, the development of biosimilars and generics are expected to experience rapid growth in 2018.
“The Japanese pharma industry has recently made attempts to attract more global business and the report findings demonstrate that there are more opportunities than ever for new players to penetrate the market, particularly in generics and biosimilars,” said brand manager of CPhI Japan, Laura Murina. “This year, CPhI Japan will continue to provide a platform for the global pharma community to convene, fostering even greater links between the domestic and international markets, and maintaining Japan’s position as a tier-one pharma business destination.”
From Amjevita to Zarxio: A Decade of US Biosimilar Approvals
March 6th 2025Since the FDA’s groundbreaking approval of Zarxio in 2015, the US biosimilars market has surged to 67 approvals across 18 originators—though the journey has been anything but smooth, with adoption facing hurdles along the way.
How AI Can Help Address Cost-Related Nonadherence to Biologic, Biosimilar Treatment
March 9th 2025Despite saving billions, biosimilars still account for only a small share of the biologics market—what's standing in the way of broader adoption and how can artificial intelligence (AI) help change that?
Will the FTC Be More PBM-Friendly Under a Second Trump Administration?
February 23rd 2025On this episode of Not So Different, we explore the Federal Trade Commission’s (FTC) second interim report on pharmacy benefit managers (PBMs) with Joe Wisniewski from Turquoise Health, discussing key issues like preferential reimbursement, drug pricing transparency, biosimilars, shifting regulations, and how a second Trump administration could reshape PBM practices.
The Banking of Biosimilars: Insights From a Leading Health Economist
February 4th 2025Biosimilars have the potential to reduce health care costs and expand patient access, but economic and policy barriers affect adoption, explored James D. Chambers, PhD, MPharm, MSc, associate professor at the Tufts Medical Center Institute for Clinical Research and Health Policy Studies, in an interview.