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PF-1805 is a recombinant polypeptide drug candidate developed by Immunoforge. It acts as a modulator of NPRL2 (NPR2-like, GATOR1 complex subunit) and targets the natriuretic peptide receptor B (NPR-B). The drug is being investigated primarily for the treatment of achondroplasia, a congenital disorder characterized by abnormal bone growth. Its mechanism involves modulation of NPRL2/NPR-B signaling pathways, which are implicated in skeletal development. PF-1805 utilizes Immunoforge's half-life extension platform technology to enable weekly dosing and potentially improve therapeutic outcomes in patients with achondroplasia[1][3].
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