Metabolic & Weight Management
Adipotide
Also known as FTPP · Fat-Targeted Proapoptotic Peptide · Prohibitin-targeting peptide · Prohibitin-targeting peptide 1 · CKGGRAKDC-GG-D(KLAKLAK)2
Adipotide is a synthetic peptidomimetic built from two linked domains: a "homing" sequence that binds a receptor complex (annexin A2 and prohibitin) reported on the endothelial cells lining white adipose tissue vasculature, and a proapoptotic sequence intended to trigger programmed cell death in those vessels, indirectly reducing fat mass. Its best-known evidence is preclinical: a 2011 study in spontaneously obese rhesus monkeys (published in Science Translational Medicine) reported weight loss and improved insulin sensitivity, alongside dose-dependent, generally reversible changes to kidney tubule structure. A Phase 1 oncology trial in patients with obesity-associated prostate cancer received FDA IND clearance around 2012 (Arrowhead), but no completed peer-reviewed human efficacy or safety results have been published, and development was discontinued. As of 2026 the evidence base remains largely animal-based with no validated human data, and nephrotoxicity is the dominant reported safety concern. Adipotide is not an approved medicine and exists only as an experimental research compound.
Studied / used for
- Investigated for reduction of white adipose tissue mass and body weight in obesity models
- Studied for effects on insulin sensitivity and markers of insulin resistance in obese primates
- Investigated as a vascular-targeting (anti-angiogenic) approach to adipose tissue in preclinical research
- Explored in early oncology research in the context of obesity-associated prostate cancer
Commonly reported side effects
- Reversible kidney effects commonly reported in animal studies, including raised serum creatinine and renal tubular changes; nephrotoxicity is the primary reported safety concern and was the dose-limiting effect in preclinical models, and is commonly cited as a reason human development did not advance
- Dehydration commonly reported
- Reduced food intake commonly reported in preclinical models
- Nausea and fatigue commonly reported
- Injection-site soreness or irritation commonly reported
Not medical advice.
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