Clinical Trial

Safety, Tolerability, and Efficacy of PLX-200 in Patients With CLN3

Not Yet Recruiting Phase 3
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Summary
The purpose of this study is to evaluate the safety and efficacy of multiple doses of PLX-200 in patients with CLN3 disease.
Protocol Amendment History 11 amendments
This ClinicalTrials.gov record has been amended 11 times since 2020-11-14; most recent amendment 2026-05-06.
Trial Details
NCT Number NCT04637282
Lead Sponsor Polaryx Therapeutics, Inc.
Conditions Juvenile Neuronal Ceroid Lipofuscinosis
Enrollment 39 participants
Start Date 2026-11-01
Primary Completion 2026-12-31 (estimated)
Study Completion 2026-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-05-08