Daiichi Sankyo extends phase I/II test on novel treatment of Duchenne muscular dystrophy (DMD)

The drug, DS-5141, is a nucleic acid medicine and has been co-developed with Orrphan Disease Treatment Institute, Tokyo. As it was not possible to obtain the expected results with regard to the main endpoint of efficacy, the administration period for the same patient will be prolonged 4fold.

Daiichi Sankyo news release, April 25, 2018

Most popular posts:

This website stores cookies on your computer. These cookies are used to provide a more personalized experience and to track your whereabouts around our website in compliance with the European General Data Protection Regulation. If you decide to to opt-out of any future tracking, a cookie will be setup in your browser to remember this choice for one year.

Accept or Deny