Under active development. Data is being added and corrected on an hourly basis.

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Tesofensine structure

Tesofensine

Metabolic
Phase 2 Research
55%
Moderate Risk
3/5

Also Known As

NS2330 ยท TE

Overview

Tesofensine is an oral serotonin-norepinephrine-dopamine reuptake inhibitor originally developed for Parkinsons and Alzheimers. Now investigated for obesity treatment. Produces significant weight loss (10-12kg in trials).

Mechanism of Action

Inhibits reuptake of serotonin, norepinephrine, and dopamine. Reduces appetite and may increase resting energy expenditure. Metabolized by CYP3A4 to active metabolite M1.

Quick Reference

Common Dose 0.25-0.5mg
Frequency 1x daily (oral)
Half-Life ~8-9 days
Storage Store at room temperature. Oral tablet.

Notes

Very long half-life (~220 hours). Once daily dosing. Phase III trials for obesity ongoing. Not FDA approved.