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Bring a scale and blood pressure cuff if you have one

Results from 327 women demonstrated: Significant increases in satisfying sexual events compared to placebo at 1.25 mg and 1.75 mg doses Improved Female Sexual Function Index total scores (mean improvement of 3.6 points vs 1.9 for placebo) Reduced sexual distress as measured by Female Sexual Distress Scale scores Dose-dependent response with optimal effects at 1.75 mg Two Phase 3 trials (RECONNECT studies) enrolled over 1,200 premenopausal women with acquired, generalized HSDD and confirmed efficacy at the 1.75 mg dose administered subcutaneously at least 45 minutes before anticipated sexual activity

Conclusion The clear advantage following the US FDA approval of resmetirom in early 2024 is the availability of the first targeted drug therapy specifically for MASH

Clin J Am Soc Nephrol 12(12):20322045

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