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combination products regulated as both a medical device and drug product
After a 2 week screening period all eligible participants were randomly assigned to treatment groups receiving either a subcutaneous injection of 2.4 mg of semaglutide, 2.4 mg of cagrilintide, a combination of cagrilintide and semaglutide, a semaglutide placebo, or a cagrilintide placebo [2]

10.1242/jeb.221606 [DOI] [PubMed] [Google Scholar] 13.Bratic A, Larsson NG

BPC-157 5 mg

This is not a basis to dismiss the work, but it is a basis to weight the absence of independent replication heavily when reading

Each capsule contains precisely measured 2mg dose enabling consistent research protocols
