DNDi recognizes the potential value, to researchers in public health and other actors, of the data gathered in the course of its research and development activities. DNDi also recognizes the ethical imperative to share and disseminate its data responsibly in order to contribute to knowledge for the improvement of lives of neglected patients whose needs are often overlooked as research priorities.
DNDi commits to sharing its clinical trial data in a manner that respects the DNDi Guiding Principles on the Sharing of Clinical Trial Data.
These Principles apply to all final (locked and analyzed) and anonymized patient-level data and clinical study reports on all clinical trials, including Phase I trials, where DNDi as Sponsor owns the generated data. When DNDi is involved in a study in the capacity other than as the Sponsor, including as a co-sponsor, DNDi will make efforts to have these principles followed by the third parties.