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, while respecting the rights of those patients.
DNDi commits to sharing its clinical trial data in a manner that respects participants in medical research and maximizes the benefits to participants and society, while minimizing any potential harm. In 2017, we signed the World Health Organization’s Joint statement on public disclosure of results from clinical trials.
You can read more about DNDi’s commitment to data sharing in the DNDi Guiding Principles on the Sharing of Clinical Trial Data.
Researchers who would like access to DNDi clinical data are requested to fill out a request form: PDF
Please send completed forms or inquiries to CTdata@dndi.org.