There is no established daily SS-31 peptide dose for general wellness, energy, or longevity. SS-31 peptide, also called elamipretide, has been studied in specific disease protocols, but online dosing ranges are not approved medical guidance. Do not self-dose; discuss eligibility, risks, and monitoring with a licensed clinician.
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See if you qualify →What is the short answer on SS-31 peptide dose per day?
The short answer: there is no universal SS-31 dose per day for general mitochondrial support. Published and registered research protocols study elamipretide in defined conditions, with defined routes and monitoring, not as an open-ended wellness peptide.
Quick facts: SS-31 dosing, approval status, and evidence limits
SS-31 dosing cannot be separated from the clinical context. A trial in primary mitochondrial myopathy, a trial in Barth syndrome, and an acute-care heart or kidney study may use different routes, endpoints, visit schedules, and safety checks 3, 4, 5. That is why a number copied from a forum is not the same as medical guidance.
Why online “daily dose” ranges can be misleading
Online peptide guides often mix clinical-trial doses, animal-study doses, and non-medical protocols. That is risky because route matters: a subcutaneous injection, intravenous infusion, eye drop, nanoparticle delivery system, or lab-cell exposure can produce very different exposure in the body 2, 6.
What is SS-31, also called elamipretide?
SS-31 is a small mitochondria-targeted peptide. Its sequence is often written as D-Arg-Dmt-Lys-Phe-NH2, and it is designed to concentrate near the inner mitochondrial membrane rather than float broadly through the cell 1.
Names to know: SS-31, elamipretide, MTP-131, Bendavia, and Szeto-Schiller peptide 31
The same molecule may appear under several names: SS-31, elamipretide, MTP-131, Bendavia, Szeto-Schiller peptide 31, or D-Arg-Dmt-Lys-Phe-NH2 1. These names can make searches confusing, especially when a wellness article, a trial registry, and a mechanistic paper use different labels.
What kind of peptide is SS-31?
SS-31 is a tetrapeptide, meaning it is made of four amino-acid building blocks. It is described as a mitochondria-targeted peptide because its chemical structure supports interactions with the inner mitochondrial membrane 1.
How SS-31 differs from general antioxidant supplements
General antioxidant supplements act more broadly and do not reliably concentrate inside mitochondria. SS-31 is different because researchers designed it to localize near mitochondrial membranes and interact with cardiolipin, a fat-like molecule involved in electron transport chain function 1.
How is SS-31 thought to work in mitochondria?
The main idea is that SS-31 may help stabilize mitochondrial membrane function under stress. Research focuses on cardiolipin, reactive oxygen species, ATP production, and mitochondrial permeability transition processes, but these mechanisms do not prove a general human longevity benefit 1.
Cardiolipin and the inner mitochondrial membrane
Cardiolipin is a key lipid in the inner mitochondrial membrane. It helps organize parts of the electron transport chain, the system cells use to help make ATP, which is the cell’s main energy currency 1.
Reactive oxygen species, ATP production, and mitochondrial stress
When mitochondria are stressed, they may produce more reactive oxygen species, often called ROS. SS-31 has been investigated for lowering mitochondrial ROS production and protecting against mitochondrial depolarization in experimental models 1.
What preclinical models can show—and what they cannot prove in humans
Preclinical studies can show whether a mechanism looks plausible in cells or animals. They cannot prove that a peptide improves energy, slows aging, or extends healthy life in people. For example, a zebrafish study of SS-31-conjugated nanoparticles looked at gentamicin-related hair-cell injury and mitochondrial targeting, not human wellness dosing 2.
What daily doses have been studied in research?
Research doses vary because clinical trials are built around a specific question. A trial dose is not a recommendation for an individual person, and it is not a general wellness protocol.
Why dose depends on the condition, route, formulation, and trial protocol
Elamipretide has appeared in studies using different routes, including subcutaneous and intravenous approaches, depending on the disease and study design 3, 5, 7. Route matters because it changes absorption, peak levels, monitoring needs, and potential side effects.
Dosing chart: separate clinical-trial dosing from non-medical internet protocols
| Context | What was studied | What it can tell you | What it cannot tell you |
|---|---|---|---|
| Primary mitochondrial myopathy trial | A registered phase 3 study evaluated subcutaneous elamipretide 40 mg once daily in adults with primary mitochondrial myopathy 3. | This shows one disease-specific trial protocol and monitoring plan. | It does not establish a daily dose for wellness, fatigue, athletic recovery, or longevity. |
| Barth syndrome trial | A registered Barth syndrome study evaluated subcutaneous elamipretide 40 mg once daily in a rare inherited mitochondrial condition 4. | This helps show how dosing is tied to a rare-disease research question. | It does not mean the same dose applies to people without that diagnosis. |
| Acute cardiac or ischemia-reperfusion research | Some studies used intravenous elamipretide or Bendavia-style protocols in acute-care settings 5, 7. | This can test short-term biologic or clinical endpoints under supervision. | It is not a home daily peptide plan. |
| Animal or zebrafish delivery models | A zebrafish lateral-line model used SS-31-conjugated PLGA nanoparticles to study gentamicin-related hair-cell protection 2. | This can teach researchers about mitochondrial targeting and drug delivery. | It should not be converted into a human dose. |
| Internet peptide protocols | Non-medical websites may list daily injection ranges without clinician evaluation. | They may reflect opinion or commercial practice. | They are not the same as FDA labeling, a trial protocol, or individualized medical care. |
Why animal or cell-study doses should not be converted into human self-dosing
Animal and cell studies often use routes, exposure levels, and delivery systems that do not match human use. In the zebrafish study, the intervention was a drug-delivery system using SS-31-conjugated nanoparticles, not plain SS-31 self-injection in people 2.
Is SS-31 approved for longevity, fatigue, or general mitochondrial support?
No established approval or guideline supports SS-31 for general longevity, fatigue, or mitochondrial optimization. Any use outside a specific approved label or clinical trial should be treated as investigational or off-label, and patients should verify the current label status through official FDA sources 8.
Approved indications versus off-label or investigational use
An approved indication means a drug has FDA-reviewed labeling for a defined use, dose, population, and safety information. A plausible mechanism, a trial registry entry, or a peptide-clinic protocol is not the same as an approved indication 8.
What counts as human clinical evidence
Human clinical evidence includes phase 1 safety studies, randomized trials, open-label extension studies, and disease-specific registries. These can be useful, but they answer narrow questions, such as whether elamipretide affects a defined endpoint in a defined disease group 3, 4, 6.
Why a plausible mitochondrial mechanism is not proof of a longevity benefit
Mitochondria are central to energy biology, but that does not mean every mitochondria-targeted compound improves human lifespan or healthspan. The kidney review notes promising experimental models but also states that renal evidence remains limited and mechanisms are still being explored 1.
What are the known safety questions with SS-31?
The honest answer is that SS-31 safety depends on the person and the protocol. Human studies are more informative than animal work, but they still may not capture long-term, unsupervised, combined, or wellness use.
Adverse effects reported in human research should be summarized cautiously
Trial registries and publications track adverse events under controlled conditions, with eligibility rules and monitoring visits 3, 4, 6. That does not tell us the full risk profile for people buying research peptides online or combining multiple compounds without medical oversight.
Special caution for people with kidney, heart, metabolic, or complex chronic conditions
SS-31 has been investigated in kidney-disease models such as ischemia-reperfusion injury, acute kidney injury, chronic kidney disease, diabetic nephropathy, and other renal contexts 1. That research interest should not be read as a green light for people with kidney, heart, or metabolic disease to self-experiment.
Why compounded or research-use peptides require extra scrutiny
The biggest safety split is licensed versus unlicensed access. A licensed clinician and a state-licensed 503A pharmacy create a different safety environment than no-prescription “research chemical” vendors, where identity, sterility, potency, and monitoring may be unclear. Compounded medications and compounded peptides are not FDA-approved.
Does Chia offer SS-31 peptide?
No. Chia does not currently offer SS-31 or elamipretide. We cover it here because patients ask about mitochondrial peptides and daily dosing, and we want the answer to be clear: SS-31 is education-only at Chia.
Chia does not currently offer SS-31 or elamipretide
SS-31 is not in our live treatment catalog, so we do not link it to a product page or present it as something available through Chia. If you are considering any peptide, the safest starting point is a licensed clinical review rather than a self-made dosing plan.
Longevity-related treatments Chia does offer: NAD+, glutathione, sermorelin, GHK-Cu cream, and Foundation Longevity
For patients who want a clinician-reviewed longevity conversation, Chia does offer NAD+ as injection or nasal spray, glutathione as injection or nasal spray, sermorelin as injection, nasal spray, or tablets, and GHK-Cu cream. We also offer Foundation Longevity, which combines sermorelin injection, NAD+ injection, and glutathione injection in one protocol.
| Chia option | Forms listed in Chia’s catalog | Current starting price | How it relates to this article |
|---|---|---|---|
| NAD+ | Injection, nasal spray | Nasal spray plans currently start at $119/mo; injection plans currently start at $179/mo | Longevity-related treatment Chia offers; not the same as SS-31. |
| Glutathione | Injection, nasal spray | Plans currently start at $179/mo | Antioxidant-related treatment Chia offers; not proof of SS-31 benefit. |
| Sermorelin | Injection, nasal spray, tablets | Injection and nasal spray plans currently start at $179/mo | Growth-hormone-axis peptide Chia offers; separate from SS-31. |
| GHK-Cu Cream | Cream | Plans currently start at $159/mo | Skin-focused peptide cream Chia offers; not a mitochondrial peptide. |
| Foundation Longevity | Sermorelin injection + NAD+ injection + glutathione injection | Plans currently start at $399/mo | A bundled Chia protocol for clinician-reviewed longevity goals. |
How Chia’s online clinician review works for treatments that are in the live catalog
For treatments Chia does offer, care starts with a short online health questionnaire. A licensed US provider reviews your history and prescribes only when clinically appropriate; a prescription is never guaranteed. If prescribed, medications are compounded by state-licensed US 503A pharmacies and shipped to your door, with provider-guided dosing and portal messaging for follow-up.
What should you ask a clinician before using any mitochondrial peptide?
Before using any mitochondrial peptide, ask whether there is a real diagnosis, a clear goal, and a monitoring plan. A daily peptide dose without a medical reason is not a safe plan.
Questions about diagnosis, goals, labs, medications, and contraindications
- What condition or symptom are we trying to evaluate?
- Is there human evidence for this goal, or only animal and cell evidence?
- What labs or records should be reviewed first?
- Could this interact with my medications, supplements, heart history, kidney function, pregnancy status, or metabolic conditions?
- What side effects should trigger stopping and seeking care?
Questions about pharmacy source, prescription status, and monitoring
- Is this being prescribed by a licensed clinician after a real evaluation?
- Is the pharmacy state-licensed, and is the product made for a specific patient prescription?
- What monitoring visits or check-ins are planned?
- How will the clinician decide whether to continue, stop, or change therapy?
- Is the product compounded, research-use only, or FDA-approved for a specific labeled use?
When to avoid self-experimentation
Avoid self-experimentation if you are pregnant or trying to become pregnant, have kidney or heart disease, have a complex neurologic or metabolic condition, take multiple prescription drugs, or bought a peptide from a no-prescription vendor. Those are situations where clinician oversight matters.
FAQ
There is no common daily SS-31 dose for wellness, energy, athletic recovery, or longevity. Some clinical trials studied protocol-defined doses in specific diseases, but those doses are not self-dosing instructions.
Daily use has been studied in some clinical-trial settings, but that does not mean daily use is appropriate for the general public. Whether any peptide is appropriate depends on diagnosis, route, risks, medications, and monitoring.
Yes. SS-31 is also called elamipretide, MTP-131, Bendavia, Szeto-Schiller peptide 31, and D-Arg-Dmt-Lys-Phe-NH2.
FDA approval status should be checked against current official FDA labeling sources. Even when a drug has an approved use, that does not make it approved for longevity, fatigue, athletic recovery, or general mitochondrial optimization.
No. SS-31 has a plausible mitochondrial mechanism and disease-focused research, but that is not proof that it extends lifespan or improves healthspan in humans.
Some wellness discussions combine mitochondrial or antioxidant-related treatments, but combination-specific human trials are limited. Chia does not offer SS-31. Chia does offer NAD+ and glutathione after clinician review when appropriate.
No. Chia does not currently offer SS-31 or elamipretide. We do offer certain longevity-related treatments in our live catalog, including NAD+, glutathione, sermorelin, GHK-Cu cream, and Foundation Longevity.
Do not inject or take it based on an internet protocol. Bring the product information to a licensed clinician or pharmacist and ask about identity, sterility, potency, interactions, and whether medical evaluation is needed.
References
- 1.Zhang Y, Zhang J, Zhang L, et al. SS-31, a mitochondria-targeting peptide, ameliorates kidney disease: mechanisms and therapeutic potential. Frontiers in Pharmacology. 2022.
- 2.Chen H, Tang L, Qin Y, et al. SS-31 peptide enables mitochondrial targeting drug delivery for protection against gentamicin-induced ototoxicity in a zebrafish model. International Journal of Nanomedicine. 2021.
- 3.ClinicalTrials.gov. A phase 3 trial of elamipretide in subjects with primary mitochondrial myopathy (MMPOWER-3), NCT03323749. 2017.
- 4.ClinicalTrials.gov. A study of elamipretide in subjects with Barth syndrome (TAZPOWER), NCT03098797. 2017.
- 5.ClinicalTrials.gov. Bendavia for prevention of reperfusion injury in patients with acute coronary events, NCT01572909. 2012.
- 6.ClinicalTrials.gov. A study of elamipretide in subjects with primary mitochondrial myopathy, NCT02367014. 2015.
- 7.ClinicalTrials.gov. A study to evaluate elamipretide in subjects with heart failure, NCT02788747. 2016.
- 8.U.S. Food and Drug Administration. Drugs@FDA: FDA-approved drugs database. 2026.
About this article
Chia Health Editorial Team — Evidence-reviewed health education
This article is for educational purposes only and is not a substitute for individualized medical advice. Talk to a licensed clinician before starting, stopping, or changing any prescription.
AI tools may assist with research and drafting. Chia's editorial team reviews source use, clarity, treatment information, and safety framing before publication. A clinician is named only after explicit sign-off. Read our editorial standards.
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