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They are not intended for human consumption, veterinary use, or any clinical application
Dosing is determined by your licensed provider based on your individual health profile and treatment goals
However, development was discontinued in 2007 after the largest Phase IIb trial failed to demonstrate statistically significant weight loss compared to placebo
Tesofensine (2 mg/kg, subcutaneously) and Clozapine-N-Oxide (CNO, 3 mg/kg, intraperitoneally), both drugs or vehicle (DMSO or saline) were administered at 18:30 (30 minutes before the dark cycle begins)
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