HomeTrialNCT05371613
🔬NCT05371613Phase 2Phase 3RECRUITING

A Study to Determine the Efficacy and Safety of Tividenofusp Alfa (DNL310) vs Idursulfase in Pediatric and Young Adult Participants With Neuronopathic (nMPS II) or Non-Neuronopathic Mucopolysaccharidosis Type II (nnMPS II)

Study Summary

This is a Phase 2/3, multiregional, two-arm, double-blind, randomized, active (standard-of-care)-controlled study of the efficacy and safety of tividenofusp alfa (DNL310), an investigational central nervous system (CNS)-penetrant enzyme-replacement therapy (ERT) for mucopolysaccharidosis type II (MPS II). Participants may also qualify to enter an open-label treatment phase with DNL310 or idursulfase based on pre-specified criteria.

Interventions / Drugs
View on ClinicalTrials.gov ↗
Study Details
Enrollment63 participants
Primary Completion
Lead SponsorDenali Therapeutics Inc.
Data Retrieved2026-04-11 04:11:49.403410+00:00
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