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Reporting of data from clinical trials comes slowly or not at all. Impending regulations in the US promise to improve the situation, but full compliance will require better incentives from institutions and a greater understanding that reporting data does not jeopardize the publication of results.
The US Food and Drug Administration's priority review voucher system for drugs to treat neglected disease has come under scrutiny for lacking preconditions that ensure fair pricing of the products that they aim to usher forward. That loophole needs to be closed.
As part of the World Health Organization (WHO) R&D Blueprint initiative, leading stakeholders on Middle East respiratory syndrome coronavirus (MERS-CoV) convened to agree on strategic public-health goals and global priority research activities that are needed to combat MERS-CoV.