Adipotide
Adipotide (FTPP) is an experimental proapoptotic peptide designed to destroy the blood supply of white fat tissue, causing fat loss. It produced weight loss in obese primates in preclinical work but also caused dose-dependent kidney toxicity. It has never been tested in a completed human efficacy trial and is not a safe or characterised human agent.
01 Overview
Adipotide is a targeting peptide fused to a proapoptotic sequence: one part homes to a marker (prohibitin) on the vasculature feeding white adipose tissue, and the other triggers apoptosis in those endothelial cells, effectively starving fat tissue of its blood supply. In obese rhesus monkeys it produced rapid, substantial weight and fat loss.
The same primate studies revealed dose-dependent renal toxicity, including changes in kidney tissue, which is a major barrier to human use. There is no completed human efficacy trial demonstrating safe weight loss, and its appearance as a research-chemical fat-loss peptide markets a compound whose best-documented finding in primates is organ toxicity.
02 Mechanism
A fusion peptide that binds prohibitin on white-adipose-tissue vasculature and delivers a proapoptotic (KLAKLAK) motif, inducing apoptosis of the fat-feeding endothelium so adipose tissue regresses.
03 Dosing
| Tier | Dose | Route | Notes |
|---|---|---|---|
| Experimental (no validated dose) | 1–5 mg/day | SubQ | No validated human dose. Primate studies used weight-based dosing associated with renal toxicity; any self-dosing is high-risk. |
04 Effects
| Effect | Magnitude | Evidence | |
|---|---|---|---|
| Fat loss / weight lossRapid weight and fat reduction shown in obese rhesus monkeys; not demonstrated safely in humans. | Marked in obese primates | Preclinical | |
| Reduced food intakeDecreased food intake accompanied fat loss in primate studies. | Observed in animals | Preclinical |
05 Side effects
| Effect | Severity | Frequency | Evidence | Countermeasures |
|---|---|---|---|---|
| Nephrotoxicity (kidney damage)Dose-dependent kidney injury observed in primate studies, the principal barrier to human development. | Severe | Dose-dependent in primates | Preclinical | |
| Unknown systemic apoptotic off-target effectsA proapoptotic agent may affect tissues beyond fat vasculature; unstudied in humans. | Severe | Uncharacterised | Unconfirmed |