RecruitingEarly Phase 1NCT05805007

Safety and Tolerability Study of Gene Editing Drug ZVS203e in Participants With Retinitis Pigmentosa

Studying OBSOLETE: Inherited retinal disorder

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Key facts

Sponsor
Peking University Third Hospital
Principal Investigator
Liping Yang, MD
Peking University Third Hospital
Intervention
ZVS203e(drug)
Enrollment
9 enrolled
Eligibility
18 years · All sexes
Timeline
20232026

Study locations (1)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT05805007 on ClinicalTrials.gov

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