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Clinical Trial Summary

This study will evaluate the safety and tolerability of ATSN-201 in male subjects ≥ 6 years of age with RS1-associated X-linked retinoschisis (XLRS).


Clinical Trial Description

Eligible patients who enroll in this study will receive a one-time subretinal injection of ATSN-201 in one eye. Safety and tolerability will be evaluated for 5 years. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05878860
Study type Interventional
Source Atsena Therapeutics Inc.
Contact Atsena Therapeutics Clinical Trials
Phone 984-261-2001
Email clinicaltrials@atsenatx.com
Status Recruiting
Phase Phase 1/Phase 2
Start date August 22, 2023
Completion date October 2029

See also
  Status Clinical Trial Phase
Recruiting NCT06066008 - Safety and Efficacy Study of Novel Gene Therapy ZM-01 for X-linked Retinoschisis Patients Early Phase 1
Completed NCT02331173 - Clinical Evaluation of Patients With X-linked Retinoschisis N/A
Completed NCT02416622 - Safety and Efficacy of rAAV-hRS1 in Patients With X-linked Retinoschisis (XLRS) Phase 1/Phase 2
Recruiting NCT05814952 - Safety and Efficacy Study of LX103 Treatment of X-Linked Retinoschisis (XLRS) N/A