SS-31
In Clinical TrialsMitochondrial Peptides · Mitochondrial Protection
SS-31 (elamipretide) is a mitochondria-targeted peptide that concentrates 1000-fold in the inner mitochondrial membrane.
What is SS-31?
SS-31 (elamipretide) is a mitochondria-targeted peptide that concentrates 1000-fold in the inner mitochondrial membrane. It protects mitochondrial function, reduces oxidative stress, and has shown promise for heart failure, mitochondrial diseases, and age-related mitochondrial decline.
Also known as: Elamipretide, Bendavia, MTP-131
How Does SS-31 Work?
Targets cardiolipin in the inner mitochondrial membrane, stabilizing cristae structure and optimizing electron transport chain function. Reduces reactive oxygen species (ROS) production at the source. Improves mitochondrial ATP production efficiency.
What is SS-31 Used For?
- Mitochondrial protection
- Heart failure
- Age-related decline
- Exercise recovery
Potential Side Effects
- Injection site reactions
- Headache
- Dizziness
Contraindications
- Pregnancy
- Children (limited data)
FDA Legal Status
United States — FDA
In Clinical TrialsThis peptide is currently investigational and not approved for clinical use.
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Frequently Asked Questions
What makes SS-31 unique?
Quick Facts
- Legal Status (USA)
- In Clinical Trials
- Evidence Rating
- BModerate Evidence (Some Human Data)
- Class / Subclass
- Mitochondrial Peptides / Mitochondrial Protection
- Administration
- subcutaneous, intravenous
- Typical Dosage
- 4mg daily (clinical trials)
- Half-Life
- ~3-4 hours
- Year Discovered
- 2004
Sources
Last updated: 2026-04-01
Sources & references
Primary sources used for the dosing, mechanism, side-effect, and regulatory claims on this page. Verify time-sensitive information (regulatory status, prescribing details) on the source before relying on it for medical decisions. See our disclaimer.
- PubMed PMID 16873680 — peer-reviewed primary literature on SS-31.
- ClinicalTrials.gov NCT02814097 — registered clinical trial; protocol, dosing, and outcome reporting per FDA / NIH standards.
- FDA Federal Register — official notice record for FDA regulatory actions and Category 1 / 503A bulk-substance updates.