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    Research bench · research use only

    Mitochondrial Bench

    SS-31, NAD+ and glutathione, with the null trials named

    no dosing on this page human data on 3 of 3 the randomized elamipretide trials ran from a single infusion to 48 weeks, with one open-label extension out to 168 weeks; the positive oral glutathione trial measured its rise at six months; no timing data exists for NAD+ by the routes sold here advanced

    Overview

    SS-31 (elamipretide), NAD+ and glutathione get sold together under one word, mitochondria. this bench separates the approved indication from the failed trials, and the routes with human data from the ones with none.

    Read this first

    all three are research use only from BHG Labs, with a third-party COA on every lot. two things before any link. first, the elamipretide that is an approved drug is a subcutaneous pharmaceutical for Barth syndrome; the research vial named '31' is not that product, and the COA is the only thing that says what it contains. second, the NAD+ atomized solution is a route with no human evidence behind it, not one paper. nothing on this page is an amount or a schedule.

    The bench: 3 compounds

    roles and evidence, not amounts. this page does not publish doses or schedules for research compounds.

    1SS-31 (elamipretide)human trials

    read the guide

    the cardiolipin binder. a tetrapeptide that concentrates on the inner mitochondrial membrane. it is a real drug: the FDA approved it on 2025-09-19 as Forzinity, a subcutaneous product to improve muscle strength in Barth syndrome patients weighing at least 30 kg, under accelerated approval that still needs a confirmatory trial.

    evidence: MMPOWER-3, the 218-patient phase 3 in primary mitochondrial myopathy, missed both primary endpoints (six-minute walk and fatigue). ReCLAIM-2 in dry AMD missed both of its primaries. TAZPOWER's randomized crossover missed its primaries; the walk-distance gain people quote comes from the open-label extension with no concurrent control.

    watch for: injection-site reactions in 80 to 100% of treated participants across the trials. the store listing is named '31', and a name on a vial does not establish that it holds elamipretide; read the COA for the sequence.

    2NAD+one small human PK study

    read the guide

    the coenzyme. the store sells the molecule itself, lyophilized and as an atomized solution. most of the human literature that sounds like it belongs to NAD+ belongs to its precursors, NR and NMN.

    evidence: a 2026 systematic review of 113 studies found no outcomes trial of IV or IM NAD+ itself. the one IV pharmacokinetic study (11 people, industry-funded) saw no rise in plasma NAD+ for two hours, with a metabolite pattern that fits the molecule being broken down before uptake. precursor trials raise blood NAD+ reliably and then mostly miss on outcomes.

    watch for: nasal NAD+ has no human data at all, only a mouse paper. neither does subcutaneous or oral intact NAD+. high-dose NR nudged homocysteine up at first.

    3Glutathionehuman trials

    read the guide

    the tripeptide antioxidant. the whole argument about it is about route.

    evidence: oral: null in Witschi 1992 and Allen 2011, positive in Richie 2015 (stores up 30 to 35% over six months and back to baseline within a month of stopping), and no outcome benefit by any route. IV: the randomized Parkinson's trial (21 patients) found no difference on UPDRS. intranasal: raises brain glutathione, but the phase 2b found neither dose better than placebo.

    watch for: seven published endotoxin-poisoning cases came from contaminated infusions, and in August 2026 the FDA reported at least 30 adverse-event cases from supplement-grade glutathione used for injection. one participant on high-dose intranasal glutathione developed cardiomyopathy.

    Form

    lyophilized vials, as sold (NAD+ also as an atomized solution)

    Human data

    an approved indication for elamipretide beside six randomized trials that missed their primary endpoints; one 11-person pharmacokinetic study for NAD+ itself; mixed, route-dependent trials for glutathione

    BHG Labs carries

    3 of 3

    Level

    advanced

    Why these together

    they are together because vendors sell them together, not because any study did. the rationale is a shared phrase, oxidative stress, and it is thin: delivered glutathione failed to move oxidation markers over six months, elamipretide's own developers moved from a scavenging model to cardiolipin binding, and the human trial of an antioxidant given during cancer radiotherapy raised second cancers. the honest reason to read them side by side is to see how different their evidence is.

    Overlap

    NAD+ and glutathione are coupled in the textbook: NADPH feeds glutathione reductase. no human study shows that supplementing NAD+ raises reduced glutathione. the only combination data anywhere is SS-31 with NMN in old mice, where each corrected a different cardiac deficit, which argues they address different problems rather than the same one.

    Conflicts

    asthma with inhaled or nebulized glutathione: a 19% FEV1 drop in mild asthmatics through sulfite formation. injecting anything sold as a supplement or research chemical: the 2026 FDA cases were supplement-grade glutathione compounded for injection, and no research vial has published sterility or endotoxin data either. cancer history: the NAD+ literature argues against boosting it without a reason, and antioxidant supplementation during radiotherapy raised second primaries. NAD+ infusions: more frequent and more severe infusion reactions than NR in one unreviewed preprint whose test article is a branded NR product. no pairing of the three has been studied in people.

    What the evidence actually is

    SS-31: one accelerated approval in Barth syndrome on a strength endpoint, a Class I statement of no benefit in primary mitochondrial myopathy, and a missed AMD trial. NAD+: no outcomes trial of the molecule by any route, one 11-person infusion study, and a precursor literature that raises blood levels and mostly misses on outcomes. glutathione: an unresolved oral debate, a null IV trial in Parkinson's, a null intranasal phase 2b, and no route with an outcome benefit.

    What people report

    people report more energy on all three. the trials that measured fatigue (MMPOWER-3) and oxidative markers (Allen 2011) did not move.

    Who It's For

    people who have seen these three sold as a set and want to know which part is a drug, which part is a precursor story, and which part is a route with no data

    What to Track

    fatigue on a fixed scale, any local reaction, sleep, resting heart rate

    Sourced at BHG Labs

    Ownership disclosure: BHG Labs and BodyHackGuide are commonly owned. When you buy from BHG Labs, the team behind this site benefits, so read the evidence sections above with that in mind. Third-party COA on every lot. Research use only. Code BHG20 takes 20% off at checkout, and the store links below apply it for you.

    Read the compound guides

    Frequently Asked Questions

    SS-31 (elamipretide), NAD+ and glutathione get sold together under one word, mitochondria. this bench separates the approved indication from the failed trials, and the routes with human data from the ones with none. it covers 3 compounds: SS-31 (elamipretide), NAD+, Glutathione. this is a reference page with no protocol on it.

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