Author/Authors :
Eshghi, Peyman Pediatric Congenital Hematologic Disorders Research Center - Shahid Beheshti University of Medical Sciences, Tehran , Amin Asnafi, Ali Ahwaz Jondishapour University - Research center for Thalassemia & Hemoglobinopathy, Ahwaz , Shamshiri, Ahmadreza Pediatric Congenital Hematologic Disorders Research Center - Shahid Beheshti University of Medical Sciences, Tehran , Alavi, Samin Pediatric Congenital Hematologic Disorders Research Center - Shahid Beheshti University of Medical Sciences, Tehran , Molavi, Mohammad Department of Pediatric Hematology and Oncology - Bandar Abbas Thalassemia Center - Hormozgan University of Medical Science, Bandar Abbas , Tamaddoni, Ahmad Department of Pediatric Hematology and Oncology - Amir Kola Hospital - Babol University of Medical Science, Mazandaran , Keikhaie, Bijan Ahwaz Jondishapour University - Research center for Thalassemia & Hemoglobinopathy, Ahwaz , Naderi, Majid Seid-ol-Shohada Hospital - Treatment Center for Special Diseases, Isfahan , Hoorfar, Hamid Seid-ol-Shohada Hospital -Treatment Center for Special Diseases, Isfahan , Ansari, Shahla Department of Pediatric Hematology and Oncology - Ali Asghar Hospital - Tehran University of Medical Science, Tehran , Azarkeivan, Azita Zafar center for thalassemia - Iranian Blood Transfusion Organization, Tehran , Arasteh, Majid Samen-ol-Hojaj Center for Special Disease, Kerman , Kourorian, Zahra Pharmacovigilance and Medical Information Manager of Ronac Pharmaceutical Company, Tehran
Abstract :
Background: Deferoxamine mesylate is still the conventional and wellknown iron chelator for patients with thalassemia major. However, due to
some marketing issues the well-known original brand, Desferal®, produced by
Novartis Pharmaceuticals Company is not as available as before. The generic
brands of Deferoxamine have been introduced in many parts of the world
including Iran; however, they are not well accepted by the physicians and patients
yet. This triple-blind randomized controlled trial was designed to compare the
efficacy and safety of a new Iranian generic and the original brand product of
Deferoxamine mesylate in Iranian patients.
Methods: The present Randomized triple-blind controlled trial research was
carried on in nine centers throughout Iran. They were randomly divided into
two similar groups and a Cross-over study was designed. 24-hour urine was
collected after subcutaneous infusion of either drugs and urinary iron excretion
was measured via atomic absorption spectrophotometer device. Acute adverse
events during and after drug infusion were recorded. Mack Nara test and p-pair
test were applied to compare two cross over interventions.
Results: 154 patients from 9 centers were enrolled in this study. There were 95
women and 59 men aged 6-34 years (mean age of 21.1years). Mean urinary iron
concentration for Desferal (intervention A) vs. Desfonak (intervention B) groups
was 22.5±22.6 vs. 21.5±16.9 mg/m2 , respectively. Mean urinary iron excretion/
Kg body weight for Desferal (intervention A) vs. Desfonak (intervention B)
groups was 0.48±0.48 vs. 0.47±0.40 mg/m2, respectively.
Conclusion: According to the results of this study, there was similarity between
efficacy and safety of the original and generic brands of deferoxamine (desferal
vs. desfonac).
Keywords :
Thalassemia major , Iron chelation , Urinary iron excretion , Atomic absorption spectrophotometry , Deferoxamine mesylate