Compound atlas
Metabolic

Tesofensine

Small molecule (oral)Prescription drug
Half-life
220h
approx. mean t½
Dose range
0.25–1 mg
typical, not prescriptive
Category
Metabolic
primary use-case
Single-dose decay
t½ = 9.2d · first-order model
~36.7d
to clear
1× t½
50%
remaining
2× t½
25%
remaining
~4× t½
6%
remaining
0%25%50%75%100%0m9.2d18.3d27.5d36.7d45.8d

How a single dose clears, assuming first-order elimination. The half-life is the biggest driver of how often you dose — start a cycle to see your own cumulative concentration curve.

Overview

An oral triple monoamine-reuptake inhibitor investigated for obesity, producing notable appetite suppression.

Mechanism of action

Inhibits reuptake of dopamine, noradrenaline, and serotonin, reducing appetite and increasing satiety.

Typical protocol

0.25–1 mg orally once daily; long half-life means slow accumulation.

Storage

Room temp, dry.

Disclaimer

This page summarizes publicly available information. None of it constitutes medical advice, prescription, or recommendation to acquire, possess, or use any compound. Many peptides described are research chemicals not approved for human use in the EU. Consult a licensed physician.