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Variations in dosage or administration can significantly impact the observed mots-c peptide benefits

Direct RA outcome data is growing, and it was one of the two medications used in the UCLA RA study

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Bodyweight decreased dose dependently with retatrutide at 36 weeks by 319% (SE 061) for the 05 mg group, 792% (128) for the 4 mg escalation group, 1037% (156) for the 4 mg group, 1681% (159) for the 8 mg slow escalation group, 1634% (165) for the 8 mg fast escalation group, and 1694% (130) for the 12 mg escalation group, versus 300% (086) with placebo and 202% (072) with 15 mg dulaglutide