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No pathway to BPC-157 approval through expedited review programs (Fast Track, Breakthrough Therapy) is currently listed in the FDA's public database
The gastrointestinal effects result primarily from delayed gastric emptying and altered gut motility
The manufacturers wouldnt have to negotiate with individual Part D plans, fight to get on formularies, or manage rebates with PBMs, and they would now have direct access to a group of patients unreachable until a generous government subsidy came into being
Nat Protoc 14:22292257
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