History

March 2005 SymBio Pharmaceuticals Limited established at Nishi-Shimbashi, Minato-ku, Tokyo
July 2005 Head office relocates to Shimbashi, Minato-ku, Tokyo
December 2005 License Agreement finalized with Astellas Pharma GmbH for SyB L-0501 (bendamustine) development & commercialization rights in Japan
March 2006 Manufacturer's License (packaging, labeling and storage) obtained from Tokyo Metropolitan Government
March 2007 License Agreement finalized with Astellas Deutschland GmbH for SyB L-0501 (bendamustine) development & commercialization rights in China (HK), Taiwan, Korea and Singapore
August 2008 License Agreement finalized with Eisai Co., Ltd. for co-development and commercialization rights of SyB L-0501 (bendamustine) in Japan
March 2009 SymBio Pharmaceuticals concludes Sublicense Agreement with Cephalon, Inc. for development and commercialization rights of bendamustine hydrochloride in China (HK)
May 2009 License Agreement finalized with Eisai Co., Ltd. for co-development and commercialization rights of SyB L-0501 (bendamustine) in Korea and Singapore
October 2010 Received Domestic Manufacturing and Marketing Approval for Anticancer Agent TREAKISYM
December 2010 Launched domestic sales of anticancer agent TREAKISYM
July 2011 Onconova and SymBio Pharmaceuticals complete License Agreement for SyB L-1101/SyB C-1101
October 2011 Listed on Osaka Securities Exchange JASDAQ Growth Market
November 2014 Head office relocates to Toranomon, Minato-ku, Tokyo
May 2016 SymBio Pharma USA, Inc. established at Menlo Park, California, USA 
August 2016 Approval for Domestic Manufacturing and Marketing of Anticancer Agent TREAKISYM for Additional Indication of Chronic Lymphocytic Leukemia
December 2016 SymBio Pharmaceuticals announces the NDA approval of TREAKISYM ®(bendamustine) for the additional indication of First-line Treatment of Low-grade Non-Hodgkin's Lymphoma and Mantle Cell Lymphoma in Japan
September 2017 Eagle Pharmaceuticals (NASDAQ: EGRX) and SymBio Pharmaceuticals completed License Agreement for bendamustine liquid formulations (RTD Injection and RI Injection) development & commercialization rights in Japan *RTD: Ready-to-dilute, RI: Rapid Infusion
July 2018 TREAKISYM®(bendamustine) has been newly included as a standard-of-care option in the Guidelines for Tumors of Hematopoietic and Lymphoid Tissues 2018
September 2019 SymBio Pharmaceuticals obtained from Chimerix (NASDAQ:CMRX) the exclusive worldwide rights to develop, manufacture, and commercialize the antiviral drug brincidofovir (BCV) excluding the prevention and treatment of smallpox
September 2020 SymBio Pharmaceuticals receives approval of TREAKISYM®Ready-To-Dilute (RTD) formulation
December 2020 Commencement of in-house sales of the anti-cancer agent TREAKISYM®
January 2021 Market Launch of TREAKISYM®Ready-To-Dilute (RTD) Formulation
March 2021 SymBio Pharmaceuticals receives approval of TREAKISYM ®(bendamustine) in combination with rituximab, and in combination with rituximab and polatuzumab vedotin for relapsed or refractory diffuse large B-cell lymphoma
April 2021 SymBio Pharmaceuticals receives approval of TREAKISYM®Ready-To-Dilute (RTD) Formulation in combination with rituximab ,and in combination with rituximab and polatuzumab vedotin for relapsed or refractory diffuse large B-cell lymphoma
February 2022 SymBio Pharmaceuticals receives approval of 10-minute Rapid Infusion (RI) administration of the TREAKISYM®Liquid Formulation
December 2023 Head office relocates within Toranomon, Minato-ku, Tokyo