New Open Source Drug Discovery Initiative Takes Aim At “Devastating” Disease 07/02/2018 by Intellectual Property Watch 3 Comments Share this:Click to share on Twitter (Opens in new window)Click to share on LinkedIn (Opens in new window)Click to share on Facebook (Opens in new window)Click to email this to a friend (Opens in new window)Click to print (Opens in new window)A consortium including the Drugs for Neglected Disease initiative has launched a groundbreaking open source drug discovery project as way to find new drugs to treat mycetoma, a “devastating disease for which current treatments are ineffective, expensive, and toxic,” the group said. According to a paper laying out the “open pharma” drug development concept, “There are many potential advantages of an open source approach, such as improved efficiency, the quality and relevance of the research, and wider participation by the scientific and patient communities; a blend of traditional and innovative financing mechanisms will have to be adopted.” The full press release on the project is reprinted below. New open source drug discovery project aims to develop mycetoma treatment A transparent, open, and cost-effective approach to developing drugs for a deeply neglected disease Geneva, Rotterdam, Sydney – 6 February 2018 The MycetOS (Mycetoma Open Source) project was launched today by the University of Sydney, Erasmus MC, and the Drugs for Neglected Diseases initiative (DNDi) to use an Open Pharma approach to discover compounds that could lead to new treatments for patients suffering from fungal mycetoma (eumycetoma), a devastating disease for which current treatments are ineffective, expensive, and toxic. As a first step in the project, the global scientific community is invited to review the manuscript, “Analogues of fenarimols as novel drug candidates for mycetoma”, which has been recently submitted with full dataset to bioRxiv, an open access biology preprint server, for review and comment by interested scientists. The manuscript shares the results of early work to screen 800 diverse, drug-like molecules for active compounds against the causative pathogen of eumycetoma, which yielded several promising new hits. These results and the associated data form the starting point for the MycetOS community, which will communicate on Twitter (@MycetOS). MycetOS will progress drug discovery efforts through community-driven, in-kind scientific contributions and a robust, fully transparent online presence. All ideas and results will be published immediately in real time to an open-access database. In addition to communicating via Twitter, the MycetOS community will use a dedicated subreddit forum for transparent interactive discussion, and use github for sharing data and key project files. “We invite anyone interested to review not only the manuscript but also the dataset, and to join this Open Pharma drug discovery project for mycetoma,” said Dr Mat Todd, Associate Professor at the University of Sydney. “Forward movement of the work looks to the participation of interested researchers and others. This is already happening successfully with a previous Open Pharma project, Open Source Malaria (@O_S_M).” The manuscript on the findings of the screening effort was co-authored by early MycetOS participants from the University of Sydney, Erasmus MC, and DNDi, and by partners at the Medicines for Malaria Venture (MMV), which provided the molecules for screening from their Stasis and open access Pathogen Boxes. “While MycetOS was developed by participants from the University of Sydney, Erasmus MC and DNDi, it is not ‘owned’ by any of us,” said Wendy van de Sande, Associate Professor, Erasmus MC. “This early work merely starts a process of discovering potential new chemical entities for eumycetoma, and we invite anyone interested to identify how they might contribute and participate as an equal partner in this search for a new treatment for this most neglected of tropical diseases.” About eumycetoma Eumycetoma is a neglected tropical infectious disease, primarily endemic in Africa, that attacks the skin, deep muscle and bone, causing devastating deformities that frequently result in amputation and permanent disability. The current antifungal treatment is neither safe, nor effective (having only a 25-35% cure rate), nor affordable. The median treatment duration is 12 months, and the treatment costs more than many local people can afford. An effective, safe, affordable and shorter-term curative treatment that is appropriate for rural settings is urgently needed. Share this:Click to share on Twitter (Opens in new window)Click to share on LinkedIn (Opens in new window)Click to share on Facebook (Opens in new window)Click to email this to a friend (Opens in new window)Click to print (Opens in new window) Related "New Open Source Drug Discovery Initiative Takes Aim At “Devastating” Disease" by Intellectual Property Watch is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.