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it was abandoned, almost certainly because no sponsor was willing to underwrite the next phase

[1] [4] The medication is administered as a once-weekly subcutaneous injection, with dosing typically initiated at 2.5 mg once weekly for 4 weeks, then increased by 2.5 mg every 4 weeks as needed and tolerated up to 15 mg

The preferred injection site will depend on the individual and the healthcare professional administering the injection

Pharmacokinetic Profile: What Clinical Studies Reveal Clinical pharmacokinetic data indicates that Retatrutide demonstrates an elimination half-life ranging from 6 to 8 days

For example, a patient presents for an office visit for pelvic pain