HG004(RPE65-IRDs)

LCA is the most common cause of inherited blindness in childhood and constitutes more than 5% of all retinal dystrophies.

HG301(RHO-adRP)

Aims to address RHO-adRP with a single course of treatment

HG202(nAMD)

Characterized by the growth of pathologic choroidal neovascularization (CNV) beneath the macula

HG204(MDS)

The candidate therapeutic, HG204, is developed using HuidaGene's proprietary gene editor delivered by AAV

HG302(DMD)

Duchenne muscular dystrophy (DMD) is a rare, fatal neuromuscular genetic disease and inherited in an X-linked recessive pattern, although de novo germline mutations occur in one-third of patients.