-
1
-
-
0038324389
-
Development of tridentate iron chelators: From desferrithiocin to ICL670
-
Nick H., Acklin P., Lattmann R., et al. Development of tridentate iron chelators: from desferrithiocin to ICL670. Curr Med Chem. 2003 ; 10: 1065-1076.
-
(2003)
Curr Med Chem
, vol.10
, pp. 1065-1076
-
-
Nick, H.1
Acklin, P.2
Lattmann, R.3
-
2
-
-
35048901389
-
Deferasirox: A review of its use in the management of transfusional chronic iron overload
-
Yang LP, Keam SJ, Keating GM Deferasirox: a review of its use in the management of transfusional chronic iron overload. Drugs. 2007 ; 67: 2211-2230.
-
(2007)
Drugs
, vol.67
, pp. 2211-2230
-
-
Yang, L.P.1
Keam, S.J.2
Keating, G.M.3
-
3
-
-
36849089638
-
Concepts and goals in the management of transfusional iron overload
-
Porter JB Concepts and goals in the management of transfusional iron overload. Am J Hematol. 2007 ; 82: 1136-1139.
-
(2007)
Am J Hematol
, vol.82
, pp. 1136-1139
-
-
Porter, J.B.1
-
4
-
-
10744230223
-
Effectiveness and safety of ICL670 in iron-loaded patients with thalassaemia: A randomised, double-blind, placebo-controlled, dose-escalation trial
-
Nisbet-Brown E., Olivieri NF, Giardina PJ, et al. Effectiveness and safety of ICL670 in iron-loaded patients with thalassaemia: a randomised, double-blind, placebo-controlled, dose-escalation trial. Lancet. 2003 ; 361: 1597-1602.
-
(2003)
Lancet
, vol.361
, pp. 1597-1602
-
-
Nisbet-Brown, E.1
Olivieri, N.F.2
Giardina, P.J.3
-
5
-
-
52249085605
-
Long-term experience with deferasirox (ICL670), a once-daily oral iron chelator, in the treatment of transfusional iron overload
-
Cappellini MD, Taher A. Long-term experience with deferasirox (ICL670), a once-daily oral iron chelator, in the treatment of transfusional iron overload. Expert Opin Pharmacother. 2008 ; 9: 2391-2402.
-
(2008)
Expert Opin Pharmacother
, vol.9
, pp. 2391-2402
-
-
Cappellini, M.D.1
Taher, A.2
-
6
-
-
38349157810
-
Effect of transfusional iron intake on response to chelation therapy in B-thalassemia major
-
Cohen AR, Glimm E., Porter JB Effect of transfusional iron intake on response to chelation therapy in B-thalassemia major. Blood. 2008 ; 111: 583-587.
-
(2008)
Blood
, vol.111
, pp. 583-587
-
-
Cohen, A.R.1
Glimm, E.2
Porter, J.B.3
-
7
-
-
33847712566
-
Deferasirox for the treatment of chronic iron overload in transfusional hemosiderosis
-
discussion 1811-1813, 1817
-
Shashaty G., Frankewich R., Chakraborti T., et al. Deferasirox for the treatment of chronic iron overload in transfusional hemosiderosis. Oncology (Williston Park). 2006 ; 20: 1799-1806, 1811 ; discussion 1811-1813, 1817.
-
(2006)
Oncology (Williston Park)
, vol.20
, pp. 1799-1806
-
-
Shashaty, G.1
Frankewich, R.2
Chakraborti, T.3
-
8
-
-
33646809736
-
Vitro blood distribution and plasma protein binding of the iron chelator deferasirox (ICL670) and its iron complex Fe-[ICL670]2 for rat, marmoset, rabbit, mouse, dog, and human
-
Weiss HM, Fresneau M., Camenisch GP, et al. In vitro blood distribution and plasma protein binding of the iron chelator deferasirox (ICL670) and its iron complex Fe-[ICL670]2 for rat, marmoset, rabbit, mouse, dog, and human. Drug Metab Dispos. 2006 ; 34: 971-975.
-
(2006)
Drug Metab Dispos
, vol.34
, pp. 971-975
-
-
Weiss, H.M.1
Fresneau, M.2
Camenisch, G.P.3
-
9
-
-
47549099814
-
Absolute oral bioavailability and disposition of deferasirox in healthy human subjects
-
Sechaud R., Robeva A., Belleli R., et al. Absolute oral bioavailability and disposition of deferasirox in healthy human subjects. J Clin Pharmacol. 2008 ; 48: 919-925.
-
(2008)
J Clin Pharmacol
, vol.48
, pp. 919-925
-
-
Sechaud, R.1
Robeva, A.2
Belleli, R.3
-
10
-
-
29744438975
-
Evaluation of ICL670, a once-daily oral iron chelator in a phase III clinical trial of beta-thalassemia patients with transfusional iron overload
-
Galanello R. Evaluation of ICL670, a once-daily oral iron chelator in a phase III clinical trial of beta-thalassemia patients with transfusional iron overload. Ann N Y Acad Sci. 2005 ; 1054: 183-185.
-
(2005)
Ann N y Acad Sci
, vol.1054
, pp. 183-185
-
-
Galanello, R.1
-
11
-
-
0034808093
-
Repaglinide: A review of its therapeutic use in type 2 diabetes mellitus
-
Culy CR, Jarvis B. Repaglinide: a review of its therapeutic use in type 2 diabetes mellitus. Drugs. 2001 ; 61: 1625-1660.
-
(2001)
Drugs
, vol.61
, pp. 1625-1660
-
-
Culy, C.R.1
Jarvis, B.2
-
12
-
-
0032700543
-
Differentiation of intestinal and hepatic cytochrome P450 3A activity with use of midazolam as an in vivo probe: Effect of ketoconazole
-
Tsunoda SM, Velez RL, von Moltke LL, et al. Differentiation of intestinal and hepatic cytochrome P450 3A activity with use of midazolam as an in vivo probe: effect of ketoconazole. Clin Pharmacol Ther. 1999 ; 66: 461-471.
-
(1999)
Clin Pharmacol Ther
, vol.66
, pp. 461-471
-
-
Tsunoda, S.M.1
Velez, R.L.2
Von Moltke, L.L.3
-
13
-
-
0033735539
-
Simvastatin does not affect CYP3A activity, quantified by the erythromycin breath test and oral midazolam pharmacokinetics, in healthy male subjects
-
Prueksaritanont T., Vega JM, Rogers JD, et al. Simvastatin does not affect CYP3A activity, quantified by the erythromycin breath test and oral midazolam pharmacokinetics, in healthy male subjects. J Clin Pharmacol. 2000 ; 40: 1274-1279.
-
(2000)
J Clin Pharmacol
, vol.40
, pp. 1274-1279
-
-
Prueksaritanont, T.1
Vega, J.M.2
Rogers, J.D.3
-
14
-
-
0037300346
-
A clinical study investigating the pharmacokinetic interaction between NN703 (tabimorelin), a potential inhibitor of CYP3A4 activity, and midazolam, a CYP3A4 substrate
-
Zdravkovic M., Olsen AK, Christiansen T., et al. A clinical study investigating the pharmacokinetic interaction between NN703 (tabimorelin), a potential inhibitor of CYP3A4 activity, and midazolam, a CYP3A4 substrate. Eur J Clin Pharmacol. 2003 ; 58: 683-688.
-
(2003)
Eur J Clin Pharmacol
, vol.58
, pp. 683-688
-
-
Zdravkovic, M.1
Olsen, A.K.2
Christiansen, T.3
-
15
-
-
0031028102
-
Effect of route of administration of fluconazole on the interaction between fluconazole and midazolam
-
Ahonen J., Olkkola KT, Neuvonen PJ Effect of route of administration of fluconazole on the interaction between fluconazole and midazolam. Eur J Clin Pharmacol. 1997 ; 51: 415-419.
-
(1997)
Eur J Clin Pharmacol
, vol.51
, pp. 415-419
-
-
Ahonen, J.1
Olkkola, K.T.2
Neuvonen, P.J.3
-
16
-
-
0033711566
-
Rifampin decreases the plasma concentrations and effects of repaglinide
-
DOI 10.1067/mcp.2000.111183
-
Niemi M., Backman JT, Neuvonen M., et al. Rifampin decreases the plasma concentrations and effects of repaglinide. Clin Pharmacol Ther. 2000 ; 68: 495-500. (Pubitemid 30953869)
-
(2000)
Clinical Pharmacology and Therapeutics
, vol.68
, Issue.5
, pp. 495-500
-
-
Niemi, M.1
Backman, J.T.2
Neuvonen, M.3
Neuvonen, P.J.4
Kivisto, K.T.5
-
17
-
-
40749152342
-
Effect of food, type of food, and time of food intake on deferasirox bioavailability: Recommendations for an optimal deferasirox administration regimen
-
Galanello R., Piga A., Cappellini MD, et al. Effect of food, type of food, and time of food intake on deferasirox bioavailability: recommendations for an optimal deferasirox administration regimen. J Clin Pharmacol. 2008 ; 48: 428-435.
-
(2008)
J Clin Pharmacol
, vol.48
, pp. 428-435
-
-
Galanello, R.1
Piga, A.2
Cappellini, M.D.3
-
18
-
-
1642265327
-
No clinically relevant CYP3A induction with the dual angiotensin- converting enzyme/ neutral endopeptidase inhibitor, M100240
-
Martin NE, Howell SR, Martin LL, et al. No clinically relevant CYP3A induction with the dual angiotensin-converting enzyme/ neutral endopeptidase inhibitor, M100240. J Clin Pharmacol. 2004 ; 44: 379-387.
-
(2004)
J Clin Pharmacol
, vol.44
, pp. 379-387
-
-
Martin, N.E.1
Howell, S.R.2
Martin, L.L.3
-
19
-
-
33644817278
-
Pioglitazone, an in vitro inhibitor of CYP2C8 and CYP3A4, does not increase the plasma concentrations of the CYP2C8 and CYP3A4 substrate repaglinide
-
Kajosaari LI, Jaakkola T., Neuvonen PJ, et al. Pioglitazone, an in vitro inhibitor of CYP2C8 and CYP3A4, does not increase the plasma concentrations of the CYP2C8 and CYP3A4 substrate repaglinide. Eur J Clin Pharmacol. 2006 ; 62: 217-223.
-
(2006)
Eur J Clin Pharmacol
, vol.62
, pp. 217-223
-
-
Kajosaari, L.I.1
Jaakkola, T.2
Neuvonen, P.J.3
-
20
-
-
33644548936
-
Telithromycin, but not montelukast, increases the plasma concentrations and effects of the cytochrome P450 3A4 and 2C8 substrate repaglinide
-
Kajosaari LI, Niemi M., Backman JT, et al. Telithromycin, but not montelukast, increases the plasma concentrations and effects of the cytochrome P450 3A4 and 2C8 substrate repaglinide. Clin Pharmacol Ther. 2006 ; 79: 231-242.
-
(2006)
Clin Pharmacol Ther
, vol.79
, pp. 231-242
-
-
Kajosaari, L.I.1
Niemi, M.2
Backman, J.T.3
|