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Clinical Trials/NCT05047523
NCT05047523
Terminated
Phase 3

A Multicenter, Randomized, Controlled, Open-label, Rater-blinded Study to Evaluate Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of ALXN1840 Versus Standard of Care in Pediatric Participants With Wilson Disease

Alexion Pharmaceuticals, Inc.1 site in 1 country40 target enrollmentSeptember 13, 2021

Overview

Phase
Phase 3
Intervention
ALXN1840
Conditions
Wilson Disease
Sponsor
Alexion Pharmaceuticals, Inc.
Enrollment
40
Locations
1
Primary Endpoint
Percent Change From Baseline to Week 48 in Non-ceruloplasmin-bound Copper in Plasma
Status
Terminated
Last Updated
last year

Overview

Brief Summary

This study is being conducted to evaluate the efficacy, safety, pharmacokinetics (PK), and pharmacodynamics of ALXN1840 versus standard of care in pediatric participants with Wilson disease (WD).

Detailed Description

Participants who complete the 48 weeks of treatment in Period 1 will have the option to receive ALXN1840 for 24 weeks in Period 2 (open-label extension). Safety will be monitored throughout the study.

Registry
clinicaltrials.gov
Start Date
September 13, 2021
End Date
June 26, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of Wilson Disease by Leipzig Score ≥
  • Adequate venous access to allow collection of required blood samples.
  • Able to swallow intact ALXN1840 tablets or mini-tablets.
  • Willing to avoid intake of foods and drinks with high contents of copper.
  • Willing and able to follow protocol-specified contraception requirements.

Exclusion Criteria

  • Decompensated hepatic cirrhosis or MELD score \> 13 (ages 12 to \<18) or PELD score \> 13 (ages 3 to \< 12).
  • Modified Nazer score \>
  • Clinically significant gastrointestinal bleed within past 3 months.
  • Alanine aminotransferase (ALT) \> 2 × upper limit of normal (ULN) for participants treated for \> 28 days with WD therapy or ALT \> 5 × ULN for treatment-naïve participants or participants who have been treated for ≤ 28 days.
  • Marked neurological disease requiring either nasogastric feeding tube or intensive inpatient medical care.
  • Hemoglobin less than lower limit of the reference range for age and sex.
  • History of seizure activity within 6 months prior to informed consent/assent.
  • Participants in renal failure, defined as in end-stage renal disease on dialysis (chronic kidney disease stage 5) or estimated glomerular filtration rate \< 30 milliliters/minute/1.73 meter squared.

Arms & Interventions

ALXN1840

ALXN1840 will be administered at one of two starting doses, with incremental dose increases permitted.

Intervention: ALXN1840

Standard of Care

Participants will receive their current therapy or initiate Standard of Care therapy.

Intervention: Standard of Care

Outcomes

Primary Outcomes

Percent Change From Baseline to Week 48 in Non-ceruloplasmin-bound Copper in Plasma

Time Frame: Baseline, Week 48

Plasma samples were planned to be collected to measure ceruloplasmin-bound copper. Due to the early termination of the study, data for this Outcome Measure were not collected for any of the cohorts.

Secondary Outcomes

  • Number of Participants With Treatment-emergent Adverse Events (TEAEs) During the Primary Evaluation Period(Baseline up to Week 48)
  • Area Under the Effect Versus Time Curve (AUEC) for Plasma Total Copper and Direct NCC(Week 48)
  • Maximum Observed Concentration (Cmax) of ALXN1840 for Plasma Total Molybdenum and Plasma Ultrafiltrate Molybdenum Concentrations(Week 48)
  • Area Under the Plasma Concentration Versus Time Curve From Time 0 to the End of the Dosing Interval (AUCtau) of ALXN1840 for Plasma Total Molybdenum and Plasma Ultrafiltrate Molybdenum(Week 48)

Study Sites (1)

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