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Clinical Trial Summary

Patients with PKAN will be treated with the iron chelator deferiprone for 18 months. Only patients who have completed the earlier study TIRCON2012V1 (NCT01741532), a double-blind placebo-controlled trial in which participants were randomized to receive either deferiprone or placebo for 18 months, are eligible to enroll.


Clinical Trial Description

TIRCON2012V1-EXT is a multi-center, single-arm, open-label study. All patients who completed the earlier study TIRCON2012V1 (NCT01741532) are eligible to take part. In the initial study, patients were randomized in a 2:1 ratio to receive 18 months of treatment with either the iron chelator deferiprone or placebo, respectively. In this extension study, all participants will receive deferiprone for 18 months. Thus, depending on which product was received earlier, patients will be on deferiprone for a total of either 1.5 years or 3 years. As in the earlier study, assessments will be carried out every six months to look at the safety of the drug and to see if patients are showing any improvement in dystonia and other symptoms of PKAN. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02174848
Study type Interventional
Source Chiesi Canada Corp
Contact
Status Completed
Phase Phase 3
Start date June 2014
Completion date March 16, 2018

See also
  Status Clinical Trial Phase
Terminated NCT03041116 - Efficacy and Safety Study of Fosmetpantotenate (RE-024) in PKAN Participants Phase 3
Active, not recruiting NCT04182763 - CoA-Z in Pantothenate Kinase-associated Neurodegeneration (PKAN) N/A
Completed NCT01741532 - Efficacy and Safety Study of Deferiprone in Patients With Pantothenate Kinase-associated Neurodegeneration (PKAN) Phase 3
No longer available NCT02635841 - Compassionate Use of Deferiprone in Patients With PKAN