Side-by-side comparison: effects, dosing ranges, side effects, regulatory status, and reconstitution.
Peptide A
Longevity
D-retro-inverso senolytic peptide — selectively kills senescent cells via FOXO4-p53 disruption.
Peptide B
Longevity
Mitochondria-targeted tetrapeptide that restores bioenergetics by stabilizing cardiolipin.
Typical vial
10 mg
Typical dose
Per kg dosing (research) mcg
Half-life
Extended via DRI backbone (~hours-days)
FDA status
Not FDA approved. In preclinical / early clinical developmen…
Typical vial
5 mg
Typical dose
5000-50000 mcg
Half-life
~4 hours
FDA status
Not FDA approved. FDA declined approval for Barth syndrome i…
FOX04-DRI effects
SS-31 (Elamipretide) effects
FOX04-DRI side effects
SS-31 (Elamipretide) side effects
FOX04-DRI dosing ranges
Senolytic research (research-only)
0.4-5 mg/kg · Every other day for 1-2 weeks per cycle · Cycle-based per protocol
SS-31 (Elamipretide) dosing ranges
Mitochondrial support and longevity
5-50 mg · Once daily (SubQ) · 4-12 weeks
FOX04-DRI: D-retro-inverso senolytic peptide — selectively kills senescent cells via FOXO4-p53 disruption. Typical dose Per kg dosing (research) mcg. SS-31 (Elamipretide): Mitochondria-targeted tetrapeptide that restores bioenergetics by stabilizing cardiolipin. Typical dose 5000-50000 mcg. Both fall under the Longevity category.
Stacking FOX04-DRI with SS-31 (Elamipretide) is a protocol-design question best raised with a clinician — it depends on your goal, current bloodwork, and whether both peptides target overlapping mechanisms. Both peptides should be tracked independently with separate injection sites and timing. PinnyPeptide supports multi-peptide stacks with automatic injection site rotation.
FOX04-DRI is typically dosed: Every other day for 1-2 weeks per cycle for Senolytic research (research-only). SS-31 (Elamipretide) is typically dosed: Once daily (SubQ) for Mitochondrial support and longevity.
FOX04-DRI: Not FDA approved. In preclinical / early clinical development as Proxofim (Cleara Biotech). SS-31 (Elamipretide): Not FDA approved. FDA declined approval for Barth syndrome in 2023, requesting additional efficacy data. Multiple clinical trials ongoing for other mitochondrial indications.
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