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Both are made by Lilly

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Safety Profile & Chemical Identity of Melanotan-2 Data from peer-reviewed publications and supplier datasheets Melanotan-2 Chemical Identity Synthetic cyclic heptapeptide analog of -MSH with lactam bridge Asp-Lys Melanotan-2 Documented Tolerance Profile Data from pilot clinical studies and peer-reviewed case reports Published clinical and preclinical data Four peer-reviewed trials and case reports Phase I pilot 1996, Wessells 1998-2000, case reports 2011-2014 2/3 Subjects with measurable pigmentation after 5 low doses of 0,01-0,03 mg/kg SC Doses studied (mg/kg SC) MC4R+ Central erectile function effects documented in double-blind crossover Evaluation method 20 years Cumulative review of Melanotan-I and Melanotan-II development since the University of Arizona Documented steps Case report Melanoma reported after Melanotan-2 injections + use of UV tanning beds Clinical context 3 generations Pharmacological evolution: MT2 (pan-MCR) bremelanotide (MC4R pref.) afamelanotide (MC1R selective) Receptor selectivity Important Notice Search Only Not intended for human consumption

The change in intracellular ROS levels was plotted as mean fluorescence intensity (MFI)

Structure Patients treated with tesamorelin for 52 weeks (T-T group) showed no change between Weeks 26 and 52 in mean trunk fat (increase of 0.1 kg in Study 1 and decrease of 0.5 kg in Study 2, respectively, compared with an increase of 1.4 kg in patients in the T-P group in Study 1 and an increase of 1.09 kg in Study 2, respectively) nor was there a change from Week 26 baseline in mean lean body mass (decrease of 0.1 kg in Study 1 and increase of 0.1 kg in Study 2, respectively, compared with a decrease of 1.8 kg in patients in the T-P group in Study 1 and a decrease of 1.7 kg in Study 2, respectively)