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Field GuideFat LossAdipotide
Fat Loss

Adipotide

FTPP · prohibitin-targeting peptide-1

A fat-targeting peptide that works by cutting off the blood supply to white adipose tissue. Striking primate results, and a phase 1 trial terminated for kidney toxicity. Included here because it is sold — not because it is recommended.

📝 Community guide · reviewed by Carl · Suggest an edit
Carl reading the research Carl read the papers
so you don’t have to.

What it actually is

Adipotide is a peptidomimetic that binds prohibitin, a protein concentrated on the blood vessels feeding white fat. It carries a second domain that triggers apoptosis — cell death — in those vessels.

The concept is unusual: rather than suppressing appetite or raising metabolic rate, it starves fat tissue of its blood supply so the tissue itself is lost. That mechanism is also the source of the problem, because the kidney is densely vascular and takes the same hit.

Carl’s one-liner: The one where the dose that works and the dose that damages your kidneys are approximately the same dose.

How it’s thought to work

What the research says

The 2011 Barnhart primate study is the famous one — obese rhesus monkeys lost roughly 11% of body weight in four weeks. Renal toxicity was described there as mild and reversible. It was not, in humans: the phase 1 clinical trial was terminated in 2019, with dose-limiting renal toxicity — raised creatinine and structural change in tubular cells. The therapeutic index is around 1.0, meaning the dose that produces meaningful fat loss is essentially the same dose that damages kidneys.

Watch: Adipotide explained

Video by Seth Spartan (The TRT King) on YouTube. Not affiliated with Peptide Carl and not an endorsement — included because a second explanation of the same mechanism is often what makes it click.

Reported protocols

These are the doses the peptide community actually reports running (Reddit & forums), alongside published research — logged for education, not as a recommendation to use.

ParameterCommonly reported range
Study protocolPublished work used 28-day cycles followed by a washout — long enough for fat reduction, intended to cap cumulative renal exposure
Circulating figures0.5 mg/kg/day for 28 days is widely repeated online. It is extrapolated from monkey studies and did not translate safely to humans
Lower figuresSome sources cite roughly 0.01 mg/kg/day as a more conservative research dose
RouteSubcutaneous
MonitoringEvery serious protocol calls for kidney function monitoring — creatinine and eGFR — from the first week
Community tipThe honest community position on this compound is largely do not run it. The people who have looked closely at the phase 1 termination generally conclude the margin is too thin to manage at home.
Reality check: This is the one compound in this directory where the safety signal is not theoretical. A human trial was stopped because of it. Renal injury in the primate work was dose-dependent, progressive and frequently irreversible. Kidney damage is also largely silent until it is advanced — you do not feel it happening, which removes the usual feedback that tells someone to stop. Nothing here is a protocol; it is a description of why one is difficult to construct safely.

Common use cases

GoalCommunity protocol notes
Adipose research28-day cycles with washout, per the published study design
Why it is not a fat-loss protocoltherapeutic index ~1.0 — no usable margin between effect and renal injury

Mixing it (reconstitution)

Freeze-dried peptides must be reconstituted with bacteriostatic water before they can be measured. Carl’s calculator turns “mg in the vial + ml of water + target dose” into “units on the syringe” — and tells you how long the vial lasts.

→ Open the Reconstitution Calculator

Injection & handling

Published research used subcutaneous administration in 28-day cycles with a washout period between them. The far more important point is monitoring: renal function — creatinine and eGFR — is the parameter that ended the human programme, and kidney injury produces no symptoms until it is well advanced. Anyone handling this compound without baseline and ongoing bloods has no way of knowing what is happening.

Stacks it appears in

Carl’s quick FAQ

Does it actually work?
In primates, clearly — around 11% body weight in four weeks. Efficacy was never the problem.
Why was the trial stopped?
Dose-limiting renal toxicity: elevated creatinine and structural damage to kidney tubular cells. Animal work had suggested this was mild and reversible; in humans it was not.
What does a therapeutic index of 1.0 mean?
That the effective dose and the harmful dose are effectively the same. Most usable drugs have a wide gap between the two. This one does not.
Is there a safe dose?
No dose has been established as safe in humans. The trial designed to find one was terminated.
The honest summary: Adipotide has the most interesting mechanism in this directory and the worst risk profile. It is documented here because it is sold and people will look it up — they should find the phase 1 termination and the therapeutic index rather than only the monkey headline. If you take one thing from this page: the fat-loss result is real, and so is the reason the human trial stopped.
Carl
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