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This analysis aimed to demonstrate the QP-A by predicting the outcomes of a proof-of-concept (PoC) trial of tesofensine in AD patients based on data from two small phase IIa trials

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You can see my testimony at the PCAC if you watch the live stream or the pre-recorded version on youtube at: Also our 5 risks of peptides, like bpc-157, is a useful resource in this area: I really think the FDA will ultimately ignore the opinion of the largely financially conflicted PCAC