Daiichi Sankyo will return all rights to develop and commercialize Translational Sciences’ investigational thrombus dissolving agent, TS23, after a successful Phase 1a clinical trial.
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[01-December-2017] |
TOKYO and PHOENIX, Dec. 1, 2017 /PRNewswire/ -- Daiichi Sankyo and Translational Sciences today announced that Daiichi Sankyo will return all rights to develop and commercialize Translational Sciences’ investigational thrombus (blood clot) dissolving agent, TS23, after a successful Phase 1a clinical trial. “Translational Sciences has been an excellent partner,” said Marielle Cohard-Radice, Executive Vice President, Global Head of Development of Daiichi Sankyo. “Our decision to terminate this agreement is based solely on our efforts to re-prioritize and re-focus our portfolio.” “While we enjoyed a successful partnership with Daiichi Sankyo, we understand the reprioritization of their portfolio,” said Guy Reed, MD of Translational Sciences. “There is a significant need for a safe, effective therapy for the millions of people who suffer from ischemic stroke, venous thromboembolism and myocardial infarction. After completing a successful Phase 1a trial, we are committed to advancing the clinical development of this novel monoclonal antibody for the benefit of patients with cardiovascular diseases.” Daiichi Sankyo took an impaired loss of approximately 2.4 billion yen (20 million U.S. dollars) in the second quarter consolidated financial result for FY2017 (IFRS), reflecting payments made in 2015 to Translational Sciences under the terms of the development agreement. About Daiichi Sankyo About Translational Sciences *This press release does not necessarily represent the official views of the National Institutes of Health. Contact: View original content:http://www.prnewswire.com/news-releases/daiichi-sankyo-and-translational-sciences-conclude-agreement-after-successful-phase-1a-trial-as-part-of-daiichi-sankyo-portfolio-prioritization-300564967.html SOURCE Daiichi Sankyo |