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The decision to terminate the clinical development of Lotiglipron was based on the pharmacokinetic data from the clinical Phase 1 drug-drug interaction studies (NCT05671653 and NCT05788328), as well as the laboratory measurements of elevated transaminases in these Phase 1 studies and the ongoing Phase 2 study (NCT05579977)

The method of embodiment 35, wherein the composition comprises from about 14 wt % to about 18 wt % poloxamer 407

therefore consultation from your doctor is recommended prior administering injections containing this substance into your body..

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PMID: 37595516