Clinical Trials Directory

Trials / Completed

CompletedNCT01741532

Efficacy and Safety Study of Deferiprone in Patients With Pantothenate Kinase-associated Neurodegeneration (PKAN)

A Randomized, Double-blind, Placebo-controlled Trial of Deferiprone in Patients With Pantothenate Kinase-associated Neurodegeneration (PKAN)

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
89 (actual)
Sponsor
ApoPharma · Industry
Sex
All
Age
4 Years
Healthy volunteers
Not accepted

Summary

A multi-center, placebo controlled, double-blind trial comparing the efficacy and safety of 18 months of treatment with deferiprone versus placebo in patients with PKAN. This investigator-initiated trial was funded by the European Commission's Seventh Framework Programme (FP7/2007-2013, HEALTH-F2-2011, grant agreement No. 277984) to the TIRCON consortium (Treat Iron-Related Childhood-Onset Neurodegeneration) and by the FDA Office of Orphan Products Development (OOPD) (Dr. Elliott Vichinsky).

Detailed description

This is a multi-center, double-blind, randomized, placebo-controlled, 18-month study in patients with PKAN aged 4 years and older. Participants are randomized in a 2:1 ratio to receive either deferiprone oral solution or placebo, twice a day for 18 months. Efficacy assessments, an MRI scan to measure iron levels in the globus pallidus, pharmacokinetic evaluations, and safety assessments are conducted at specified time points. Following completion of the trial, eligible patients are invited to enroll in an 18-month extension study, TIRCON2012V1-EXT, in which all participants receive deferiprone.

Conditions

Interventions

TypeNameDescription
DRUGDeferiprone oral solutionDeferiprone 80 mg/mL oral solution will be administered twice daily (b.i.d.) for 18 months. An initial dose of 5 mg/kg b.i.d. will be administered for 6 weeks. The dose will then be escalated to 10 mg/kg b.i.d. and finally to 15 mg/kg b.i.d.
DRUGPlaceboA deferiprone matching placebo oral solution will be given twice daily for 18 months.

Timeline

Start date
2012-12-13
Primary completion
2016-10-21
Completion
2017-01-11
First posted
2012-12-05
Last updated
2019-07-05
Results posted
2019-05-23

Locations

4 sites across 4 countries: United States, Germany, Italy, United Kingdom

Source: ClinicalTrials.gov record NCT01741532. Inclusion in this directory is not an endorsement.