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Serapha Bio is a privately held clinical-stage biotechnology company developing in vivo base editing therapies for Alpha-1 Antitrypsin Deficiency. The company emerged publicly on June 23, 2026 alongside an announced reverse merger with Boundless Bio and a concurrent $230 million financing. Its lead program, SERP-01, is designed to correct the SERPINA1 E342K (PiZZ) mutation, the most common severe genetic cause of AATD. SERP-01 was licensed in June 2026 from YolTech Therapeutics, where it had been developed as YOLT-202 for Greater China. Serapha is positioning the asset as a potentially best-in-class, one-time genetic medicine for liver and lung disease associated with AATD.
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