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1 contribution to Research Peptide Community
SS-31 gets FDA approval for treatment of rare disease
9/19/25 the U.S. Food and Drug Administration granted accelerated approval to Forzinity (elamipretide) injection as the first treatment for Barth syndrome, in patients weighing at least 30 kg. Barth syndrome is a rare, serious and life-threatening disease of the mitochondria (the energy-producing parts of cells). https://www.fda.gov/news-events/press-announcements/fda-grants-accelerated-approval-first-treatment-barth-syndrome
5 likes • Oct '25
My daughter has special needs - and a few of our friends kids have rare genetic mitochondrial diseases…. Makes me hopeful for the research.
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Kate Peden
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@kate-peden-3507
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Active 10h ago
Joined Aug 26, 2025
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