SS-31 (Elamipretide)
A mitochondria-targeting tetrapeptide (D-Arg-dimethylTyr-Lys-Phe-NH2) that concentrates in the inner mitochondrial membrane and binds cardiolipin, aiming to stabilise cristae and improve energy production. Unlike most peptides here it has been through multiple human trials in mitochondrial and cardiovascular disease, though pivotal efficacy has been mixed.
01 Overview
Elamipretide (SS-31, MTP-131) selectively accumulates in mitochondria and associates with cardiolipin, protecting cristae architecture and reducing reactive oxygen species during energy stress. It has been studied in primary mitochondrial myopathy, heart failure, dry AMD and other conditions, giving it a genuine — if inconclusive — human evidence base.
Several trials showed biomarker or subgroup signals but missed primary endpoints, so it remains investigational. Grey-market SS-31 is sold for anti-ageing and performance, well ahead of the clinical evidence, which does not support those uses.
02 Mechanism
Binds cardiolipin in the inner mitochondrial membrane, stabilising cristae, improving electron transport efficiency and reducing reactive oxygen species.
03 Dosing
| Tier | Dose | Route | Notes |
|---|---|---|---|
| Trial dose | 40 mg/day | SubQ | Common daily subcutaneous dose used in mitochondrial myopathy trials. |
04 Effects
| Effect | Magnitude | Evidence | |
|---|---|---|---|
| Improved mitochondrial energeticsTrials reported improvements in some functional and biomarker measures, though primary endpoints were often not met. | Biomarker and subgroup changes | Clinical | |
| Reduced oxidative stressPreclinical models show reduced reactive oxygen species and preserved cristae under stress. | Lower ROS in models | Preclinical |
05 Side effects
| Effect | Severity | Frequency | Evidence | Countermeasures |
|---|---|---|---|---|
| Injection-site reactionsRedness, itching or induration at subcutaneous injection sites, the most frequently reported adverse effect in trials. | Mild | Common | Clinical | |
| Gastrointestinal upsetNausea and diarrhoea reported in some trial participants. | Mild | Uncommon | Clinical |