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After the FDA approval, Palatins European partner (Gedeon Richter) was evaluating the Phase 3 data for a possible EU application, but as of the latest updates, it appears no EMA approval has been granted for female HSDD or any use
Securing back-to-back authorizations from two of the world's most demanding regulators -- for a product class where peptide stability, device compatibility and analytical comparability have historically delayed generic entry -- underscores the scientific and quality robustness of Orbicular's program
Participants who had received the placebo up to week 80, achieved an average of 19.2% reduction in body weight at 104 weeks after switching to the maximum tolerated dose of retatrutide
Type 2 diabetes
Of course, 2025 is far from over Im sure that through books, podcast guests, conferences, and my continued focus on immersive journalism, research, and self-guinea-pigging, Ill discover plenty more biohacks to share with you
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