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Description
GEP44 was developed based on extensive structureactivity relationship studies and earlier preliminary in vivo studies that demonstrated its greater efficacy at reducing both food intake and body weight compared to the agonist peptide, Ex-4, without triggering gastrointestinal distress (as assessed by kaolin intake and behavioral scoring as a proxy for nausea in rats and direct evidence of emesis in shrews) 16
Many health plans don't cover the drugs
This study suggests there may be drugs that are soon available for OSA
Not sure which drivers apply to you
Untangling the ErbB signalling network
