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COMPLETEDNCT01838291

Active Drug Surveillance Program of Ferriprox Use

Observational, open label, prospective, multi-center, post-marketing drug surveillance program.

Lead sponsor: ApoPharma•14 locations•View source on ClinicalTrials.gov

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What this study is about

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Sponsors

Lead Sponsor

ApoPharma

A post-marketing, drug surveillance program evaluating the use, monitoring, benefits and adverse effects of Ferriprox under clinical conditions in newly treated patients.

Age

All ages

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•Patients who started Ferriprox therapy less than one month or are to initiate Ferriprox therapy at the time of enrolment into the program.

Exclusion Criteria

•Patients treated with Ferriprox for more than one month prior to enrolment.

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: April 24, 2013Terms

Trial snapshot

StatusCOMPLETED

Phase—

Enrollment294

Start dateJun 2010

Last updatedApr 24, 2013

Condition

Transfusional Iron Overload

Locations shown

Thalassemia Center of North Cyprus Turkish Republic (KKTC)

Nicosia

Hematology Unit, Mansoura University Children Hospital

Al Mansurah

Hematology Unit, El-Shatby Children Hospital, Alexandria University

Alexandria

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: April 24, 2013Data synced to Clareo: May 17, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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