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NCT07240896

A Clinical Study on the Treatment of Wilson Disease With ATP7B mRNA/LNP (DSL101)

Recruiting now EARLY_PHASE1 Last updated 15 January 2026
What this trial tests

EARLY_PHASE1 trial testing Group 1: DSL101 Low dose in Wilsons Disease in 18 participants. Currently enrolling.

Timeline
31 December 2025
Primary endpoint
1 April 2028
1 April 2029

Quick facts

Lead sponsorDSciLab Co., Ltd.
PhaseEARLY_PHASE1
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationnon randomized
Designsequential
Maskingnone
Primary purposetreatment
Enrollment18
Start date31 December 2025
Primary completion1 April 2028
Estimated completion1 April 2029
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

DSciLab Co., Ltd. — full company profile →

Who can join

18 and older, any sex, with Wilsons Disease. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

This study adopted an open, single-arm, non-randomized, dose-escalation research design, aiming to evaluate the safety, tolerability, preliminary efficacy, pharmacokinetic and immunogenicity characteristics of single and multiple intravenous infusions of DSL101 in patients with Wilson's disease.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07240896.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing