نتایج جستجو برای: deferasirox

تعداد نتایج: 613  

Journal: :The Journal of antimicrobial chemotherapy 2010
Ashraf S Ibrahim Teclegiorgis Gebremariam Samuel W French John E Edwards Brad Spellberg

OBJECTIVES Increased bone marrow iron levels in patients with haematological malignancies is an independent risk factor for developing invasive pulmonary aspergillosis (IPA), suggesting an important role for iron uptake in the pathogenesis of IPA. We sought to determine the potential for combination therapy with the iron chelator deferasirox + liposomal amphotericin B (LAmB) to improve the outc...

2012
Jong Gwon Choi Jung-Lim Kim Joohee Park Soonwook Lee Seh Jong Park Jun Suk Kim Chul Won Choi

BACKGROUND Iron is essential for cell proliferation and viability. It has been reported that iron depletion by a chelator inhibits proliferation of some cancer cells. Deferasirox is a new oral iron chelator, and a few reports have described its effects on lymphoma cells. The goal of this study was to determine the anticancer effects of deferasirox in malignant lymphoma cell lines. METHODS Thr...

2011
Michihide Tokuhira Morihiko Sagawa Reiko Watanabe Tomoe Nemoto Takeshi Tomikawa Shigehisa Mori Masahiro Kizaki

Introduction: Deferasirox is an oral iron chelator, approved worldwide for the treatment of chronic iron overload due to transfusion. Deferasirox was permitted two years ago in Japan, but there is little known regarding its efficacy and tolerability in clinical practice. Methods: We conducted a retrospective study of 18 patients with transfusion-dependent anemias treated by deferasirox at our i...

2014
Ali T Taher John B Porter Vip Viprakasit Antonis Kattamis Suporn Chuncharunee Pranee Sutcharitchan Noppadol Siritanaratkul Raffaella Origa Zeynep Karakas Dany Habr Zewen Zhu M Domenica Cappellini

OBJECTIVE Patients with non-transfusion-dependent thalassemia (NTDT) often develop iron overload and related complications, and may require iron chelation. However, the risk of over-chelation emerges as patients reach low, near-normal body iron levels and dose adjustments may be needed. In the THALASSA study, the threshold for chelation interruption was LIC <3 mg Fe/g dw (LIC<3); 24 patients re...

Journal: :British Journal of Haematology 2007
Elliott Vichinsky Onyinye Onyekwere John Porter Paul Swerdlow James Eckman Peter Lane Beatrice Files Kathryn Hassell Patrick Kelly Felicia Wilson Françoise Bernaudin Gian Luca Forni Iheanyi Okpala Catherine Ressayre-Djaffer Daniele Alberti Jaymes Holland Peter Marks Ellen Fung Roland Fischer Brigitta U Mueller Thomas Coates

Deferasirox is a once-daily, oral iron chelator developed for treating transfusional iron overload. Preclinical studies indicated that the kidney was a potential target organ of toxicity. As patients with sickle cell disease often have abnormal baseline renal function, the primary objective of this randomised, open-label, phase II trial was to evaluate the safety and tolerability of deferasirox...

Journal: :Blood 2011
M Domenica Cappellini Mohamed Bejaoui Leyla Agaoglu Duran Canatan Marcello Capra Alan Cohen Guillermo Drelichman Marina Economou Slaheddine Fattoum Antonis Kattamis Yurdanur Kilinc Silverio Perrotta Antonio Piga John B Porter Louis Griffel Victor Dong Joan Clark Yesim Aydinok

Patients with β-thalassemia require lifelong iron chelation therapy from early childhood to prevent complications associated with transfusional iron overload. To evaluate long-term efficacy and safety of once-daily oral iron chelation with deferasirox, patients aged ≥ 2 years who completed a 1-year, phase 3, randomized trial entered a 4-year extension study, either continuing on deferasirox (de...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2008
Gerard J M Bruin Thomas Faller Hansjörg Wiegand Alain Schweitzer Hanspeter Nick Josef Schneider K-Olaf Boernsen Felix Waldmeier

Deferasirox (Exjade, ICL670, CGP72670) is an iron-chelating drug for p.o. treatment of transfusional iron overload in patients with beta-thalassemia or sickle cell disease. The pharmacokinetics and disposition of deferasirox were investigated in rats. The animals received single intravenous (10 mg/kg) or p.o. (10 or 100 mg/kg) doses of 14C-radiolabeled deferasirox. Biological samples were analy...

Journal: :The Journal of clinical investigation 2007
Ashraf S Ibrahim Teclegiorgis Gebermariam Yue Fu Lin Lin Mohamed I Husseiny Samuel W French Julie Schwartz Christopher D Skory John E Edwards Brad J Spellberg

Mucormycosis causes mortality in at least 50% of cases despite current first-line therapies. Clinical and animal data indicate that the presence of elevated available serum iron predisposes the host to mucormycosis. Here we demonstrate that deferasirox, an iron chelator recently approved for use in humans by the US FDA, is a highly effective treatment for mucormycosis. Deferasirox effectively c...

2011
Elliott Vichinsky Françoise Bernaudin Gian Luca Forni Renee Gardner Kathryn Hassell Matthew M Heeney Baba Inusa Abdullah Kutlar Peter Lane Liesl Mathias John Porter Cameron Tebbi Felicia Wilson Louis Griffel Wei Deng Vanessa Giannone Thomas Coates

To date, there is a lack of long-term safety and efficacy data for iron chelation therapy in transfusion-dependent patients with sickle cell disease (SCD). To evaluate the long-term safety and efficacy of deferasirox (a once-daily oral iron chelator), patients with SCD completing a 1-year, Phase II, randomized, deferoxamine (DFO)-controlled study entered a 4-year extension, continuing to receiv...

Journal: :Acta haematologica 2009
M D Cappellini A Taher

Deferasirox is a once-daily oral iron chelator with established dose-dependent efficacy in both adult and pediatric patients with transfusional iron overload. The clinical development program has demonstrated the efficacy of deferasirox for up to 4.5 years of treatment in patients with various underlying anemias, including beta-thalassemia, myelodysplastic syndromes, sickle cell disease, aplast...

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