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All peptides
Research vial labelled SS-31, a Mitochondrial and metabolic peptide studied in preclinical and clinical literature

SS-31

Elamipretide

The file here is mostly preclinical work plus clinic and community practice, not registrational trials.

Targets cardiolipin on the inner mitochondrial membrane. It has been through real phase III work in mitochondrial myopathy with mixed endpoints.

General profile

Class
Mitochondrial and metabolic
Evidence
Mixed or moderate evidence
Studied dose range
5–10 mg
Frequency in protocols
Daily in trial protocols
Route
Subcutaneous
Half life
~2 hours
Reconstitution
2 mL bacteriostatic water per 50 mg vial
Storage
Refrigerated, ~30 days

Timing and cycling in the literature

Usually dosed in the morning window

Daily in trial protocols

Mitochondrial energetics are measured across the active day in the trials, so morning dosing matches the study design.

Reported cycle: 8 weeks on, 4 weeks off

Mitochondrial myopathy trials dosed daily across months to reach measurable endpoints.

Watch for: Injection site reactions, which were the most common finding in the trials.

What it conflicts with

Three separate questions, kept separate. A hard stop means the mechanisms must not run together at all and timing does not fix it. A syringe rule means the same day is fine but one barrel is not. Redundancy is not dangerous, it is paying twice to hit one target.

No named pair conflicts are on file for this compound. That is missing data, not clearance: with no compatibility data the default is separate syringes, and you still introduce one new compound at a time.

Most syringe compatibility claims here are practice and expert consensus, not peer reviewed mixing studies. A clear liquid after mixing does not prove the compounds are still active, and cloudiness, particles or gelling means discard. Active cancer, pregnancy, major cardiac care and heavy immunosuppression override every stack preference on this page.

See how SS-31 fits your week

The injection scheduler spaces doses using the clinical timing data, flags the pairs above before you draw them, and tells you why.

Model this in the injection scheduler

The studies

Human trials: No completed human efficacy trial that establishes a dose for the use people are chasing.

Open questions: Treat published dosing as observed practice, not a validated protocol.

Published papers

Indexed from Europe PMC and refreshed weekly. Each link opens the paper itself.

Search the full literature