-
1
-
-
0034843846
-
Mechanisms of action of the novel sulfonamide anticancer agent E7070 on cell cycle progression in human non - small cell lung cancer cells
-
Fukuoka K, Usuda J, Iwamoto Y, et al. Mechanisms of action of the novel sulfonamide anticancer agent E7070 on cell cycle progression in human non - small cell lung cancer cells. Invest New Drugs 2001;19:219-27.
-
(2001)
Invest New Drugs
, vol.19
, pp. 219-227
-
-
Fukuoka, K.1
Usuda, J.2
Iwamoto, Y.3
-
2
-
-
0036866878
-
E7070: A novel synthetic sulfonamide targeting the cell cycle progression for the treatment of cancer
-
van Kesteren C, Beijnen JH, Schellens JHM. E7070: a novel synthetic sulfonamide targeting the cell cycle progression for the treatment of cancer. Anticancer Drugs 2002;13:989-97.
-
(2002)
Anticancer Drugs
, vol.13
, pp. 989-997
-
-
van Kesteren, C.1
Beijnen, J.H.2
Schellens, J.H.M.3
-
3
-
-
3242712108
-
A phase II clinical and pharmacodynamic study of E7070 in patients with metastatic, recurrent, or refractory squamous cell carcinoma of the head and neck: Modulation of retinoblastoma protein phosphorylation by a novel chloroindolyl sulfonamide cell cycle inhibitor
-
Haddad RI, Weinstein LJ, Wieczorek TJ, et al. A phase II clinical and pharmacodynamic study of E7070 in patients with metastatic, recurrent, or refractory squamous cell carcinoma of the head and neck: modulation of retinoblastoma protein phosphorylation by a novel chloroindolyl sulfonamide cell cycle inhibitor. Clin Cancer Res 2004;10:4680-7.
-
(2004)
Clin Cancer Res
, vol.10
, pp. 4680-4687
-
-
Haddad, R.I.1
Weinstein, L.J.2
Wieczorek, T.J.3
-
4
-
-
33644512888
-
A phase II multicenter study of the cyclin-dependent kinase inhibitor indisulam in patients with inoperable and/or metastatic renal cell carcinoma (RCC) [abstract]
-
Edition
-
Raftopoulos H, Escudier B, Renshaw G, et al.: A phase II multicenter study of the cyclin-dependent kinase inhibitor indisulam in patients with inoperable and/or metastatic renal cell carcinoma (RCC) [abstract]. J Clin Oncol American Society of Clinical Oncology Annual Meeting Proceedings (Post-Meeting Edition) 2004;22:414s.
-
(2004)
J Clin Oncol American Society of Clinical Oncology Annual Meeting Proceedings (Post-Meeting
, vol.22
-
-
Raftopoulos, H.1
Escudier, B.2
Renshaw, G.3
-
5
-
-
19944427395
-
Phase II study of E7070 in patients with metastatic melanoma
-
Smyth JF, Aamdal S, Awada A, et al. Phase II study of E7070 in patients with metastatic melanoma. Ann Oncol 2005;16:158-61.
-
(2005)
Ann Oncol
, vol.16
, pp. 158-161
-
-
Smyth, J.F.1
Aamdal, S.2
Awada, A.3
-
6
-
-
33646795512
-
A multi center phase II study of E7070, a chloroindolyl-sulfonamide anticancer agent in anthracycline and taxane pre treated breast cancer [abstract]
-
Fumoleau P, Viens P, Cottu PH, et al. A multi center phase II study of E7070, a chloroindolyl-sulfonamide anticancer agent in anthracycline and taxane pre treated breast cancer [abstract]. 26th San Antonio Breast Cancer Symposium 2003.
-
(2003)
26th San Antonio Breast Cancer Symposium
-
-
Fumoleau, P.1
Viens, P.2
Cottu, P.H.3
-
7
-
-
0242421438
-
A phase II and pharmacodynamic study of E7070 in patients with non - small cell lung cancer (NSCLC) who have failed platinum-based chemotherapy [abstract]
-
Talbot DC, Norbury C, Slade M, et al. A phase II and pharmacodynamic study of E7070 in patients with non - small cell lung cancer (NSCLC) who have failed platinum-based chemotherapy [abstract]. Proc Am Soc Clin Oncol 2002;21:327a.
-
(2002)
Proc Am Soc Clin Oncol
, vol.21
-
-
Talbot, D.C.1
Norbury, C.2
Slade, M.3
-
8
-
-
0000902909
-
A multicentre randomised phase II study of E7070 in patients with colorectal cancer who have failed 5-fluorouracil-based chemotherapy [abstract]
-
Mainwaring PN, Van Cutsem E, Van Laethem JL, et al. A multicentre randomised phase II study of E7070 in patients with colorectal cancer who have failed 5-fluorouracil-based chemotherapy [abstract]. Proc Am Soc Clin Oncol 2002;21:153a.
-
(2002)
Proc Am Soc Clin Oncol
, vol.21
-
-
Mainwaring, P.N.1
Van Cutsem, E.2
Van Laethem, J.L.3
-
9
-
-
0037102283
-
Phase I and pharmacokinetic study of E7070, a novel chloroindolyl sulfonamide cell-cycle inhibitor, administered as a one-hour infusion every three weeks in patients with advanced cancer
-
Raymond E, ten Bokkel Huinink WW, Taieb J, et al. Phase I and pharmacokinetic study of E7070, a novel chloroindolyl sulfonamide cell-cycle inhibitor, administered as a one-hour infusion every three weeks in patients with advanced cancer. J Clin Oncol 2002;20:3508-21.
-
(2002)
J Clin Oncol
, vol.20
, pp. 3508-3521
-
-
Raymond, E.1
ten Bokkel Huinink, W.W.2
Taieb, J.3
-
10
-
-
0034772246
-
Phase I and pharmacokinetic study of E7070, a novel sulfonamide, given at a daily times five schedule in patients with solid tumors. A study by the EORTC-early clinical studies group (ECSG)
-
Punt CJA, Fumoleau P, van de Walle B, Faber MN, Ravic M, Campone M. Phase I and pharmacokinetic study of E7070, a novel sulfonamide, given at a daily times five schedule in patients with solid tumors. A study by the EORTC-early clinical studies group (ECSG). Ann Oncol 2001;12:1289-93.
-
(2001)
Ann Oncol
, vol.12
, pp. 1289-1293
-
-
Punt, C.J.A.1
Fumoleau, P.2
van de Walle, B.3
Faber, M.N.4
Ravic, M.5
Campone, M.6
-
11
-
-
0038402755
-
Phase I clinical and pharmacokinetic study of E7070, a novel sulfonamide given as a 5-day continuous infusion repeated every 3 weeks in patients with solid tumours. A study by the EORTC Early Clinical Study Group (ECSG)
-
Terret C, Zanetta S, Roche H, et al. Phase I clinical and pharmacokinetic study of E7070, a novel sulfonamide given as a 5-day continuous infusion repeated every 3 weeks in patients with solid tumours. A study by the EORTC Early Clinical Study Group (ECSG). Eur J Cancer 2003;39:1097-104.
-
(2003)
Eur J Cancer
, vol.39
, pp. 1097-1104
-
-
Terret, C.1
Zanetta, S.2
Roche, H.3
-
12
-
-
0242525657
-
Phase I and pharmacokinetic study of E7070, a chloroindolylsulfonamide anticancer agent, administered on a weekly schedule to patients with solid tumors
-
Dittrich C, Dumez H, Calvert H, et al. Phase I and pharmacokinetic study of E7070, a chloroindolylsulfonamide anticancer agent, administered on a weekly schedule to patients with solid tumors. Clin Cancer Res 2003;9:5195-204.
-
(2003)
Clin Cancer Res
, vol.9
, pp. 5195-5204
-
-
Dittrich, C.1
Dumez, H.2
Calvert, H.3
-
13
-
-
4243296525
-
Combined results of 4 phase I and pharmacokinetic studies of E7070, a novel chloroindoly-sulphonamide inhibiting the activation of cdk2 and cyclin E [abstract]
-
4529s
-
Raymond E, Fumoleau P, Roche H, et al. Combined results of 4 phase I and pharmacokinetic studies of E7070, a novel chloroindoly-sulphonamide inhibiting the activation of cdk2 and cyclin E [abstract]. Clin Cancer Res 2000;6:4529s.
-
(2000)
Clin Cancer Res
, vol.6
-
-
Raymond, E.1
Fumoleau, P.2
Roche, H.3
-
14
-
-
28444465958
-
Phase I pharmacokinetic and pharmacogenomic study of E7070 administered once every 21 days
-
Yamada Y, Yamamoto N, Shimoyama T, et al. Phase I pharmacokinetic and pharmacogenomic study of E7070 administered once every 21 days. Cancer Sci 2005;96:721-8.
-
(2005)
Cancer Sci
, vol.96
, pp. 721-728
-
-
Yamada, Y.1
Yamamoto, N.2
Shimoyama, T.3
-
15
-
-
0036789730
-
Population pharmacokinetics of the novel anticancer agent E7070 during four phase I studies: Model building and validation
-
van Kesteren C, Mathôt RAA, Raymond E, et al. Population pharmacokinetics of the novel anticancer agent E7070 during four phase I studies: model building and validation. J Clin Oncol 2002;20:4065-73.
-
(2002)
J Clin Oncol
, vol.20
, pp. 4065-4073
-
-
van Kesteren, C.1
Mathôt, R.A.A.2
Raymond, E.3
-
16
-
-
33748660661
-
A semi-physiological population pharmacokinetic model describing the non-linear disposition of indisulam
-
Zandvliet AS, Schellens JHM, Copalu W, Beijnen JH, Huitema ADR. A semi-physiological population pharmacokinetic model describing the non-linear disposition of indisulam. J Pharmacokinet Pharmacodyn 2006;33:543-70.
-
(2006)
J Pharmacokinet Pharmacodyn
, vol.33
, pp. 543-570
-
-
Zandvliet, A.S.1
Schellens, J.H.M.2
Copalu, W.3
Beijnen, J.H.4
Huitema, A.D.R.5
-
17
-
-
21044442985
-
Semi-physiological model describing the hematological toxicity of the anti-cancer agent indisulam
-
van Kesteren C, Zandvliet AS, Karlsson MO, et al. Semi-physiological model describing the hematological toxicity of the anti-cancer agent indisulam. Invest New Drugs 2005;23:225-34.
-
(2005)
Invest New Drugs
, vol.23
, pp. 225-234
-
-
van Kesteren, C.1
Zandvliet, A.S.2
Karlsson, M.O.3
-
18
-
-
0036746940
-
An excretion balance and pharmacokinetic study of the novel anticancer agent E7070 in cancer patients
-
van den Bongard HJGD, Pluim D, Rosing H, et al. An excretion balance and pharmacokinetic study of the novel anticancer agent E7070 in cancer patients. Anticancer Drugs 2002;13:807-14.
-
(2002)
Anticancer Drugs
, vol.13
, pp. 807-814
-
-
van den Bongard, H.J.G.D.1
Pluim, D.2
Rosing, H.3
-
19
-
-
22144492896
-
Human metabolism of [(14)C]indisulam following i.v. infusion in cancer patients
-
Beumer JH, Hillebrand MJX, Pluim D, et al. Human metabolism of [(14)C]indisulam following i.v. infusion in cancer patients. Invest New Drugs 2005;23:317-30.
-
(2005)
Invest New Drugs
, vol.23
, pp. 317-330
-
-
Beumer, J.H.1
Hillebrand, M.J.X.2
Pluim, D.3
-
20
-
-
0033105118
-
Integrated cytochrome P450 reaction phenotyping: Attempting to bridge the gap between cDNA-expressed cytochromes P450 and native human liver microsomes
-
Rodrigues AD. Integrated cytochrome P450 reaction phenotyping: attempting to bridge the gap between cDNA-expressed cytochromes P450 and native human liver microsomes. Biochem Pharmacol 1999;57:465-80.
-
(1999)
Biochem Pharmacol
, vol.57
, pp. 465-480
-
-
Rodrigues, A.D.1
-
21
-
-
9644279613
-
Quantitative determination of the novel anticancer drug E7070 (indisulam) and its metabolite (1,4-benzene disulphonamide) in human plasma, urine and faeces by high-performance liquid chromatography coupled with electrospray ionization tandem mass spectrometry
-
Beumer JH, Rosing H, Hillebrand MJX, et al. Quantitative determination of the novel anticancer drug E7070 (indisulam) and its metabolite (1,4-benzene disulphonamide) in human plasma, urine and faeces by high-performance liquid chromatography coupled with electrospray ionization tandem mass spectrometry. Rapid Commun Mass Spectrom 2004;18:2839-48.
-
(2004)
Rapid Commun Mass Spectrom
, vol.18
, pp. 2839-2848
-
-
Beumer, J.H.1
Rosing, H.2
Hillebrand, M.J.X.3
-
22
-
-
84869875294
-
Center for Drug Evaluation and Research (CDER)
-
U.S. Department of Health and Human Services, Food and Drug Administration
-
U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER). Guidance for Industry: Bioanalytical Method Validation. 2001.
-
(2001)
Guidance for Industry: Bioanalytical Method Validation
-
-
-
23
-
-
0028044085
-
Identification of a new genetic defect responsible for the polymorphism of (S)-mephenytoin metabolism in Japanese
-
De Morais SM, Wilkinson GR, Blaisdell J, Meyer UA, Nakamura K, Goldstein JA. Identification of a new genetic defect responsible for the polymorphism of (S)-mephenytoin metabolism in Japanese. Mol Pharmacol 1994;46:594-8.
-
(1994)
Mol Pharmacol
, vol.46
, pp. 594-598
-
-
De Morais, S.M.1
Wilkinson, G.R.2
Blaisdell, J.3
Meyer, U.A.4
Nakamura, K.5
Goldstein, J.A.6
-
24
-
-
0028260641
-
The major genetic defect responsible for the polymorphism of S-mephenytoin metabolism in humans
-
De Morais SM, Wilkinson GR, Blaisdell J, Nakamura K, Meyer UA, Goldstein JA. The major genetic defect responsible for the polymorphism of S-mephenytoin metabolism in humans. J Biol Chem 1994;269:15419-22.
-
(1994)
J Biol Chem
, vol.269
, pp. 15419-15422
-
-
De Morais, S.M.1
Wilkinson, G.R.2
Blaisdell, J.3
Nakamura, K.4
Meyer, U.A.5
Goldstein, J.A.6
-
25
-
-
0037131892
-
CYP2C9 allelic variants: Ethnic distribution and functional significance
-
Xie HG, Prasad HC, Kim RB, Stein CM. CYP2C9 allelic variants: ethnic distribution and functional significance. Adv Drug Deliv Rev 2002;54:1257-70.
-
(2002)
Adv Drug Deliv Rev
, vol.54
, pp. 1257-1270
-
-
Xie, H.G.1
Prasad, H.C.2
Kim, R.B.3
Stein, C.M.4
-
26
-
-
0344512432
-
Genetic polymorphisms of CYP2C9 and CYP2C19 in the Beninese and Belgian populations
-
Allabi AC, Gala JL, Desager JP, Heusterspreute M, Horsmans Y. Genetic polymorphisms of CYP2C9 and CYP2C19 in the Beninese and Belgian populations. Br J Clin Pharmacol 2003;56:653-7.
-
(2003)
Br J Clin Pharmacol
, vol.56
, pp. 653-657
-
-
Allabi, A.C.1
Gala, J.L.2
Desager, J.P.3
Heusterspreute, M.4
Horsmans, Y.5
-
27
-
-
0035217171
-
Identification of a null allele of CYP2C9 in an African-American exhibiting toxicity to Phenytoin
-
Kidd RS, Curry TB, Gallagher S, Edeki T, Blaisdell J, Goldstein JA. Identification of a null allele of CYP2C9 in an African-American exhibiting toxicity to Phenytoin. Pharmacogenetics 2001;11:803-8.
-
(2001)
Pharmacogenetics
, vol.11
, pp. 803-808
-
-
Kidd, R.S.1
Curry, T.B.2
Gallagher, S.3
Edeki, T.4
Blaisdell, J.5
Goldstein, J.A.6
-
28
-
-
0032716358
-
Allelic, genotypic and phenotypic distributions of S-mephenytoin 4′-hydroxylase (CYP2C19) in healthy Caucasian populations of European descent throughout the world
-
Xie HG, Stein CM, Kim RB, Wilkinson GR, Flockhart DA, Wood AJ. Allelic, genotypic and phenotypic distributions of S-mephenytoin 4′-hydroxylase (CYP2C19) in healthy Caucasian populations of European descent throughout the world. Pharmacogenetics 1999;9:539-49.
-
(1999)
Pharmacogenetics
, vol.9
, pp. 539-549
-
-
Xie, H.G.1
Stein, C.M.2
Kim, R.B.3
Wilkinson, G.R.4
Flockhart, D.A.5
Wood, A.J.6
-
29
-
-
0030904031
-
Frequencies of the defective CYP2C19 alleles responsible for the mephenytoin poor metabolizer phenotype in various Oriental, Caucasian
-
Goldstein JA, Ishizaki T, Chiba K, et al. Frequencies of the defective CYP2C19 alleles responsible for the mephenytoin poor metabolizer phenotype in various Oriental, Caucasian, Saudi Arabian and American black populations. Pharmacogenetics 1997;7:59-64.
-
(1997)
Saudi Arabian and American black populations. Pharmacogenetics
, vol.7
, pp. 59-64
-
-
Goldstein, J.A.1
Ishizaki, T.2
Chiba, K.3
-
30
-
-
15444340367
-
A new genetic defect in human CYP2C19: Mutation of the initiation codon is responsible for poor metabolism of S-mephenytoin
-
Ferguson RJ, De Morais SM, Benhamou S, et al. A new genetic defect in human CYP2C19: mutation of the initiation codon is responsible for poor metabolism of S-mephenytoin. J Pharmacol Exp Ther 1998;284:356-61.
-
(1998)
J Pharmacol Exp Ther
, vol.284
, pp. 356-361
-
-
Ferguson, R.J.1
De Morais, S.M.2
Benhamou, S.3
-
31
-
-
8244249473
-
Differences in the incidence of the CYP2C19 polymorphism affecting the S-mephenytoin phenotype in Chinese Han and Bai populations and identification of a new rare CYP2C19 mutant allele
-
Xiao ZS, Goldstein JA, Xie HG, et al. Differences in the incidence of the CYP2C19 polymorphism affecting the S-mephenytoin phenotype in Chinese Han and Bai populations and identification of a new rare CYP2C19 mutant allele. J Pharmacol Exp Ther 1997;281:604-9.
-
(1997)
J Pharmacol Exp Ther
, vol.281
, pp. 604-609
-
-
Xiao, Z.S.1
Goldstein, J.A.2
Xie, H.G.3
-
32
-
-
0032159423
-
Identification of new human CYP2C19 alleles (CYP2C19*6 and CYP2C19*2B) in a Caucasian poor metabolizer of mephenytoin
-
Ibeanu GC, Goldstein JA, Meyer U, et al. Identification of new human CYP2C19 alleles (CYP2C19*6 and CYP2C19*2B) in a Caucasian poor metabolizer of mephenytoin. J Pharmacol Exp Ther 1998;286:1490-5.
-
(1998)
J Pharmacol Exp Ther
, vol.286
, pp. 1490-1495
-
-
Ibeanu, G.C.1
Goldstein, J.A.2
Meyer, U.3
-
33
-
-
0030587544
-
Allelic variants of human cytochrome P450 2C9: Baculovirus-mediated expression, purification, structural characterization, substrate stereoselectivity, and prochiral selectivity of the wild-type and I359L mutant forms
-
Haining RL, Hunter AP, Veronese ME, Trager WF, Rettie AE. Allelic variants of human cytochrome P450 2C9: baculovirus-mediated expression, purification, structural characterization, substrate stereoselectivity, and prochiral selectivity of the wild-type and I359L mutant forms. Arch Biochem Biophys 1996;333:447-58.
-
(1996)
Arch Biochem Biophys
, vol.333
, pp. 447-458
-
-
Haining, R.L.1
Hunter, A.P.2
Veronese, M.E.3
Trager, W.F.4
Rettie, A.E.5
-
34
-
-
0029658591
-
The role of the CYP2C9-359 allelic variant in the tolbutamide polymorphism
-
Sullivan-Klose TH, Ghanayem BI, Bell DA, et al. The role of the CYP2C9-359 allelic variant in the tolbutamide polymorphism. Pharmacogenetics 1996;6:341-9.
-
(1996)
Pharmacogenetics
, vol.6
, pp. 341-349
-
-
Sullivan-Klose, T.H.1
Ghanayem, B.I.2
Bell, D.A.3
-
35
-
-
0034921210
-
Identification and functional characterization of a new CYP2C9 variant (CYP2C9*5) expressed among African Americans
-
Dickmann LJ, Rettie AE, Kneller MB, et al. Identification and functional characterization of a new CYP2C9 variant (CYP2C9*5) expressed among African Americans. Mol Pharmacol 2001;60:382-7.
-
(2001)
Mol Pharmacol
, vol.60
, pp. 382-387
-
-
Dickmann, L.J.1
Rettie, A.E.2
Kneller, M.B.3
-
36
-
-
4644293405
-
Population pharmacokinetics I: Background, concepts, and models
-
Ette EI, Williams PJ. Population pharmacokinetics I: background, concepts, and models. Ann Pharmacother 2004;38:1702-6.
-
(2004)
Ann Pharmacother
, vol.38
, pp. 1702-1706
-
-
Ette, E.I.1
Williams, P.J.2
|