SS-31 (Elamipretide): NuPOWER Phase 3 Data and Genotype-Dependent Response in POLG at Euromit 2026
Stealth BioTherapeutics announces new Elamipretide data for Euromit 2026: NuPOWER Phase 3 with genotype-dependent response in the POLG1 subgroup.
Important note: This article is intended solely for scientific information and research purposes. SS-31 is a research peptide and is not intended for human consumption. No therapeutic recommendations are given.
TL;DR: What was announced
Date: May 26, 2026, press release from Stealth BioTherapeutics. What: At Euromit 2026 (May 31 to June 4, Angers, France), new Elamipretide data will be presented, including the NuPOWER Phase 3 results in primary mitochondrial disease with indications of a genotype-dependent response in the POLG1 subgroup. Also: the design of a confirmatory study in Barth syndrome as well as preclinical POLG models. Context: This is an announcement of upcoming conference presentations, not a full data release. SS-31 is the cardiolipin-binding research twin of Elamipretide.
Mitochondria-targeted tetrapeptide (Elamipretide) that stabilizes cardiolipin and prevents ROS formation at the source.
SS-31 and Elamipretide: the same mechanism, two names
SS-31 (also known as Elamipretide) is a small, mitochondria-targeted peptide. It binds to cardiolipin in the inner mitochondrial membrane, a phospholipid that is crucial for organizing the respiratory chain and for the efficiency of energy production. Through this cardiolipin binding, SS-31 is thought to stabilize the membrane structure and improve mitochondrial function in stressed tissue. It is precisely this mechanism that makes the peptide interesting for research into mitochondrial diseases.
What will be shown at Euromit 2026
According to Stealth BioTherapeutics, the presentations will take place on June 4, 2026, in a session on therapeutic and diagnostic developments. Three topics are at the center:
- NuPOWER Phase 3: overall results of a Phase 3 study of Elamipretide in primary mitochondrial disease, presented among other things in a poster on the overall results.
- Genotype-dependent response: an emerging signal that the underlying mutation could co-determine the treatment response, with a focus on the POLG1 subgroup.
- Barth syndrome: the design of a confirmatory study as well as preclinical POLG models as the next steps of the pipeline.
Important: announcement, not full publication
This is the announcement of upcoming conference presentations, not a complete, peer-reviewed data release. Terms such as "emerging indications" and "supports the potential" come from the release and are deliberately phrased with caution. Reliable conclusions are only possible after the full data presentation and peer review.
Why the POLG1 subgroup is interesting
POLG encodes the catalytic subunit of the mitochondrial DNA polymerase gamma. Mutations in POLG are among the most common causes of primary mitochondrial disease. A "genotype-dependent response" would mean that patients with a particular genetic cause respond more strongly or more weakly to a cardiolipin-targeted strategy than others.
From a research perspective, this is an important point: mitochondrial diseases are genetically very heterogeneous, and studies in mixed populations can easily dilute effects. If a subgroup (here POLG1) turns out to be particularly responsive, this provides a hypothesis for more targeted confirmatory studies. This is exactly the path Stealth outlines with the announced confirmatory Barth design and the preclinical POLG models.
Placing it within the SS-31 pipeline
Where NuPOWER stands
NuPOWER addresses primary mitochondrial disease as an indication. This is to be distinguished from other Elamipretide programs that have been reported on separately, for example in Barth syndrome and in ophthalmology. The POLG1 findings announced here are a new subgroup signal from the primary mitochondrial disease study and are not identical to those earlier readouts.
For research on SS-31 as a longevity- and mitochondria-relevant peptide, the Euromit 2026 announcement is notable above all because it links the cardiolipin mechanism to a genetically defined patient group. This is the transition from "does it work" to "in whom does it work," which is necessary for any targeted further development.
Mitochondria-targeted tetrapeptide (Elamipretide) that stabilizes cardiolipin and prevents ROS formation at the source.
FAQ
Sources
- Stealth BioTherapeutics. "Stealth BioTherapeutics to Present Updates on Elamipretide in Barth Syndrome and POLG Disease at Euromit 2026." PR Newswire, May 26, 2026. https://www.prnewswire.com/news-releases/stealth-biotherapeutics-to-present-updates-on-elamipretide-in-barth-syndrome-and-polg-disease-at-euromit-2026-302779660.html
Research disclaimer: All content is intended solely for scientific information. SS-31 is not intended for human consumption. The content mentioned comes from an announcement of upcoming conference presentations and does not replace a peer-reviewed publication.
Research context for English-speaking buyers
Most of our English-speaking customers ship to the UK, Ireland, Malta or other English-as-second-language EU territories. The regulatory picture differs per country.
- Relevant authorities
- MHRA (UK, post-Brexit), HPRA (Ireland, EU-aligned), FDA Section 503A bulks list (US, restricted Cat 2 status of several peptides as of 2026)
- Customs and VAT
- EU shipments include 19% VAT; UK shipments after Brexit are now extra-EU and may attract UK VAT plus a handling fee at import
- Typical shipping window
- EU 2-4 working days, UK 4-7 working days, other international 7-14 working days, depending on customs
Research-grade peptides shipped from our EU warehouse are sold for laboratory use only and are not authorised for human or veterinary therapeutic application in any of the destination jurisdictions. US customers should be aware that the FDA Section 503A bulks list classification (and the April 2026 reclassification of twelve compounds) only governs compounding pharmacies, not direct-to-researcher imports for non-clinical work. UK buyers should declare the consignment on import and may be asked for a research justification by HMRC. We provide a CoA per batch identified by colour code rather than serial number; customs sometimes asks for this document when clearing the parcel.