SS-31 (Elamipretide) Dosage and Protocols
SS-31 (Elamipretide) dosage protocols reported in published research, plus reconstitution and storage.
Approved vs. Research Dosing
The FDA-approved Barth syndrome regimen uses a pre-filled subcutaneous formulation dosed daily; research-vendor protocols commonly cite around 40mg subcutaneous daily from a reconstituted vial, mirroring the approved dose. Outside the approved indication, there's no validated dose-finding data to guide use.
Reported protocol doses
Reconstitution
A 40mg vial with 2mL of bacteriostatic water is the pairing reported most often. Research-vendor convention: 40mg vial reconstituted with 2mL bacteriostatic water. The FDA-approved Barth syndrome product is a pre-filled subcutaneous formulation, not a lyophilized research vial.
Work out your own concentration with the reconstitution calculator.
Doses shown are those reported in published research, not a recommendation.