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Homology Medicines Announces Presentations on HMI-203 Investigational Gene Therapy for Hunter Syndrome and Broad Applicability of AAVHSC Platform for Lysosomal Storage Disorders at the 18th Annual WORLDSymposium™ Meeting

- Data Supported juMPStart Trial Evaluating One-Time, Systemic Administration of HMI-203 in ERT-Treated Adults - - Details of HMI-203 Clinical Trial Design and Encouraging Preclinical Data. | February 10, 2022

Theresa mcneelyCara mayfieldAlbert seymourCompany contactsCorporate communicationsSystemic administrationHomology medicines incGlobenewswire incTrial evaluating one timeTreated adultsTrial designEncouraging preclinical data featuredPlatform presentationsChief scientific officerGene therapyMucopolysaccharidosis type

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