Raw, unthresholded statistical maps are publicly available on NeuroVault ( Study approval The trial protocol and drug were approved by the ethics committee of North, West, and Central Switzerland (EKNZ, Basel, Switzerland) and the national agency for the authorization and supervision of therapeutic products (Swissmedic, Berne, Switzerland)
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Duration: 2-4 weeks intensive phase, followed by 4-8 weeks standard protocol
The FDA issues warning letters requiring the company to cease prohibited marketing claims, reformulate the product, or stop selling it entirely
The research and development costs required to bring a new product to market are substantial with no guarantee that the product will ever become profitable
[PubMed] Naghedi-Baghdar, H., Nematy, M., Kooshyar, M