-
1
-
-
33748451151
-
Anticancer activities of histone deacetylase inhibitors
-
16955068 10.1038/nrd2133 1:CAS:528:DC%2BD28XptVCltrY%3D
-
Bolden JE, Peart MJ, Johnstone RW (2006) Anticancer activities of histone deacetylase inhibitors. Nat Rev Drug Discov 5:769-784
-
(2006)
Nat Rev Drug Discov
, vol.5
, pp. 769-784
-
-
Bolden, J.E.1
Peart, M.J.2
Johnstone, R.W.3
-
2
-
-
67349228774
-
Development of the pan-DAC inhibitor panobinostat (LBH589): Successes and challenges
-
19344997 10.1016/j.canlet.2009.02.019 1:CAS:528:DC%2BD1MXmsF2jtL4%3D
-
Atadja P (2009) Development of the pan-DAC inhibitor panobinostat (LBH589): successes and challenges. Cancer Lett 280:233-241
-
(2009)
Cancer Lett
, vol.280
, pp. 233-241
-
-
Atadja, P.1
-
3
-
-
61849144810
-
HDAC family: What are the cancer relevant targets?
-
18824292 10.1016/j.canlet.2008.08.016 1:CAS:528:DC%2BD1MXjtFOhsL4%3D
-
Witt O, Deubzer HE, Milde T, Oehme I (2009) HDAC family: what are the cancer relevant targets? Cancer Lett 277:8-21
-
(2009)
Cancer Lett
, vol.277
, pp. 8-21
-
-
Witt, O.1
Deubzer, H.E.2
Milde, T.3
Oehme, I.4
-
4
-
-
84872886875
-
PANORAMA 2: A phase II study of panobinostat in combination with bortezomib and dexamethasone in patients with relapsed and bortezomib-refractory multiple myeloma
-
Alsina M, Schlossman RL, Weber DM, Coutre SE, Lonial S, Gasparetto C, Warsi G, Ondovik MS, Mukhopadhyay S, Paley CS, Richardson PGG (2012) PANORAMA 2: a phase II study of panobinostat in combination with bortezomib and dexamethasone in patients with relapsed and bortezomib-refractory multiple myeloma. ASCO Meet Abstr 30:8012
-
(2012)
ASCO Meet Abstr
, vol.30
, pp. 8012
-
-
Alsina, M.1
Schlossman, R.L.2
Weber, D.M.3
Coutre, S.E.4
Lonial, S.5
Gasparetto, C.6
Warsi, G.7
Ondovik, M.S.8
Mukhopadhyay, S.9
Paley, C.S.10
Richardson, P.G.G.11
-
5
-
-
84886919481
-
Phase III study of panobinostat with bortezomib and dexamethasone in patients with relapsed multiple myeloma (PANORAMA 1)
-
e18572
-
San-Miguel JF, Moreau P, Yoon S, Dimopoulos MA, VT de M Hungria, Wiktor-Jedrzejczak W, Elghandour A, Corradini P, Gunther A, Beksac M, Yong K, Lee JH, Lonial S, Hou J, Einsele H, Wroclawska-Swacha M, Weber H, Bourquelot P, Richardson PG (2012) Phase III study of panobinostat with bortezomib and dexamethasone in patients with relapsed multiple myeloma (PANORAMA 1). ASCO Ann Meet Abstr e18572
-
(2012)
ASCO Ann Meet Abstr
-
-
San-Miguel, J.F.1
Moreau, P.2
Yoon, S.3
Dimopoulos, M.A.4
De Hungria, M.V.5
Wiktor-Jedrzejczak, W.6
Elghandour, A.7
Corradini, P.8
Gunther, A.9
Beksac, M.10
Yong, K.11
Lee, J.H.12
Lonial, S.13
Hou, J.14
Einsele, H.15
Wroclawska-Swacha, M.16
Weber, H.17
Bourquelot, P.18
Richardson, P.G.19
-
6
-
-
84867573822
-
Characterizing the disposition, metabolism, and excretion of an orally active pan-deacetylase inhibitor, panobinostat, via trace radiolabeled 14C material in advanced cancer patients
-
22864948 10.1007/s00280-012-1940-9 1:CAS:528:DC%2BC38XhsVentb3J
-
Clive S, Woo MM, Nydam T, Kelly L, Squier M, Kagan M (2012) Characterizing the disposition, metabolism, and excretion of an orally active pan-deacetylase inhibitor, panobinostat, via trace radiolabeled 14C material in advanced cancer patients. Cancer Chemother Pharmacol 70:513-522
-
(2012)
Cancer Chemother Pharmacol
, vol.70
, pp. 513-522
-
-
Clive, S.1
Woo, M.M.2
Nydam, T.3
Kelly, L.4
Squier, M.5
Kagan, M.6
-
7
-
-
80054703794
-
Effect of ketoconazole-mediated CYP3A4 inhibition on clinical pharmacokinetics of panobinostat (LBH589), an orally active histone deacetylase inhibitor
-
Hamberg P, Woo MM, Chen LC, Verweij J, Porro MG, Zhao L, Li W, van der Biessen D, Sharma S, Hengelage T, de Jonge M (2011) Effect of ketoconazole-mediated CYP3A4 inhibition on clinical pharmacokinetics of panobinostat (LBH589), an orally active histone deacetylase inhibitor. Cancer Chemother Pharmacol
-
(2011)
Cancer Chemother Pharmacol
-
-
Hamberg, P.1
Woo, M.M.2
Chen, L.C.3
Verweij, J.4
Porro, M.G.5
Zhao, L.6
Li, W.7
Van Der Biessen, D.8
Sharma, S.9
Hengelage, T.10
De Jonge, M.11
-
8
-
-
84856749798
-
The effect of food on the bioavailability of panobinostat, an orally active pan-histone deacetylase inhibitor, in patients with advanced cancer
-
22057852 10.1007/s00280-011-1758-x 1:CAS:528:DC%2BC38XhsVOktbc%3D
-
Shapiro GI, Frank R, Dandamudi UB, Hengelage T, Zhao L, Gazi L, Porro MG, Woo MM, Lewis LD (2012) The effect of food on the bioavailability of panobinostat, an orally active pan-histone deacetylase inhibitor, in patients with advanced cancer. Cancer Chemother Pharmacol 69:555-562
-
(2012)
Cancer Chemother Pharmacol
, vol.69
, pp. 555-562
-
-
Shapiro, G.I.1
Frank, R.2
Dandamudi, U.B.3
Hengelage, T.4
Zhao, L.5
Gazi, L.6
Porro, M.G.7
Woo, M.M.8
Lewis, L.D.9
-
9
-
-
77956551464
-
Panobinostat (LBH589) pharmacokinetics (PK): Implication for clinical safety and efficacy
-
viii161 [abstract 487P]
-
Woo MM, Culver K, Li W, Liu A, Scott J, Parker K, Jalaluddin M, Laird G, Cooper MR, Schran HF (2008) Panobinostat (LBH589) pharmacokinetics (PK): implication for clinical safety and efficacy. Ann Oncol 19:viii161 [abstract 487P]
-
(2008)
Ann Oncol
, vol.19
-
-
Woo, M.M.1
Culver, K.2
Li, W.3
Liu, A.4
Scott, J.5
Parker, K.6
Jalaluddin, M.7
Laird, G.8
Cooper, M.R.9
Schran, H.F.10
-
10
-
-
0029820670
-
Constitutive expression of hepatic cytochrome P450 genes
-
8751713 1:CAS:528:DyaK28Xlt1KlsLw%3D
-
Gonzalez FJ, Lee YH (1996) Constitutive expression of hepatic cytochrome P450 genes. FASEB J 10:1112-1117
-
(1996)
FASEB J
, vol.10
, pp. 1112-1117
-
-
Gonzalez, F.J.1
Lee, Y.H.2
-
11
-
-
36148976077
-
Influence of cytochrome P450 polymorphisms on drug therapies: Pharmacogenetic, pharmacoepigenetic and clinical aspects
-
18001838 10.1016/j.pharmthera.2007.09.004 1:CAS:528:DC%2BD2sXhtlCrs7bE
-
Ingelman-Sundberg M, Sim SC, Gomez A, Rodriguez-Antona C (2007) Influence of cytochrome P450 polymorphisms on drug therapies: pharmacogenetic, pharmacoepigenetic and clinical aspects. Pharmacol Ther 116:496-526
-
(2007)
Pharmacol Ther
, vol.116
, pp. 496-526
-
-
Ingelman-Sundberg, M.1
Sim, S.C.2
Gomez, A.3
Rodriguez-Antona, C.4
-
12
-
-
0030712325
-
CYP2D6 genotype and phenotyping by determination of dextromethorphan and metabolites in serum of healthy controls and of patients under psychotropic medication
-
9429230 10.1097/00008571-199712000-00003 1:STN:280:DyaK1c%2FptV2hug%3D%3D
-
Kohler D, Hartter S, Fuchs K, Sieghart W, Hiemke C (1997) CYP2D6 genotype and phenotyping by determination of dextromethorphan and metabolites in serum of healthy controls and of patients under psychotropic medication. Pharmacogenetics 7:453-461
-
(1997)
Pharmacogenetics
, vol.7
, pp. 453-461
-
-
Kohler, D.1
Hartter, S.2
Fuchs, K.3
Sieghart, W.4
Hiemke, C.5
-
13
-
-
10744232330
-
Pharmaceutical Research and Manufacturers of America (PhRMA) Drug Metabolism/Clinical Pharmacology Technical Working Group, FDA Center for Drug Evaluation and Research (CDER) (2003) the conduct of in vitro and in vivo drug-drug interaction studies: A Pharmaceutical Research and Manufacturers of America (PhRMA) perspective
-
Bjornsson TD, Callaghan JT, Einolf HJ, Fischer V, Gan L, Grimm S, Kao J, King SP, Miwa G, Ni L, Kumar G, McLeod J, Obach RS, Roberts S, Roe A, Shah A, Snikeris F, Sullivan JT, Tweedie D, Vega JM, Walsh J, Wrighton SA, Pharmaceutical Research and Manufacturers of America (PhRMA) Drug Metabolism/Clinical Pharmacology Technical Working Group, FDA Center for Drug Evaluation and Research (CDER) (2003) The conduct of in vitro and in vivo drug-drug interaction studies: a Pharmaceutical Research and Manufacturers of America (PhRMA) perspective. Drug Metab Dispos 31:815-832
-
Drug Metab Dispos
, vol.31
, pp. 815-832
-
-
Bjornsson, T.D.1
Callaghan, J.T.2
Einolf, H.J.3
Fischer, V.4
Gan, L.5
Grimm, S.6
Kao, J.7
King, S.P.8
Miwa, G.9
Ni, L.10
Kumar, G.11
McLeod, J.12
Obach, R.S.13
Roberts, S.14
Roe, A.15
Shah, A.16
Snikeris, F.17
Sullivan, J.T.18
Tweedie, D.19
Vega, J.M.20
Walsh, J.21
Wrighton, S.A.22
more..
-
14
-
-
70349386728
-
Polymorphism of human cytochrome P450 2D6 and its clinical significance: Part i
-
19817501 10.2165/11318030-000000000-00000 1:CAS:528:DC%2BD1MXhsFOmt7rP
-
Zhou SF (2009) Polymorphism of human cytochrome P450 2D6 and its clinical significance: Part I. Clin Pharmacokinet 48:689-723
-
(2009)
Clin Pharmacokinet
, vol.48
, pp. 689-723
-
-
Zhou, S.F.1
-
15
-
-
0025321225
-
A dose-effect study of the in vivo inhibitory effect of quinidine on sparteine oxidation in man
-
2310654 10.1111/j.1365-2125.1990.tb03639.x 1:STN:280:DyaK3c7otFagtA%3D%3D
-
Nielsen MD, Brosen K, Gram LF (1990) A dose-effect study of the in vivo inhibitory effect of quinidine on sparteine oxidation in man. Br J Clin Pharmacol 29:299-304
-
(1990)
Br J Clin Pharmacol
, vol.29
, pp. 299-304
-
-
Nielsen, M.D.1
Brosen, K.2
Gram, L.F.3
-
16
-
-
0031038038
-
Cytochrome P450 2D6 variants in a Caucasian population: Allele frequencies and phenotypic consequences
-
9012401 1:CAS:528:DyaK2sXhtVCju74%3D
-
Sachse C, Brockmoller J, Bauer S, Roots I (1997) Cytochrome P450 2D6 variants in a Caucasian population: allele frequencies and phenotypic consequences. Am J Hum Genet 60:284-295
-
(1997)
Am J Hum Genet
, vol.60
, pp. 284-295
-
-
Sachse, C.1
Brockmoller, J.2
Bauer, S.3
Roots, I.4
-
17
-
-
0036124107
-
CYP2D6 allele frequency in European Caucasians, Asians, Africans and their descendants
-
11972444 10.1517/14622416.3.2.229 1:CAS:528:DC%2BD38XitlWqu70%3D
-
Bradford LD (2002) CYP2D6 allele frequency in European Caucasians, Asians, Africans and their descendants. Pharmacogenomics 3:229-243
-
(2002)
Pharmacogenomics
, vol.3
, pp. 229-243
-
-
Bradford, L.D.1
-
18
-
-
4444268162
-
Pharmacokinetics of dextromethorphan after single or multiple dosing in combination with quinidine in extensive and poor metabolizers
-
15342614 10.1177/0091270004269521 1:CAS:528:DC%2BD2cXosVWhu7w%3D
-
Pope LE, Khalil MH, Berg JE, Stiles M, Yakatan GJ, Sellers EM (2004) Pharmacokinetics of dextromethorphan after single or multiple dosing in combination with quinidine in extensive and poor metabolizers. J Clin Pharmacol 44:1132-1142
-
(2004)
J Clin Pharmacol
, vol.44
, pp. 1132-1142
-
-
Pope, L.E.1
Khalil, M.H.2
Berg, J.E.3
Stiles, M.4
Yakatan, G.J.5
Sellers, E.M.6
-
19
-
-
0034594628
-
New guidelines to evaluate the response to treatment in solid tumors. European Organization for Research and Treatment of Cancer, National Cancer Institute of the United States, National Cancer Institute of Canada
-
10655437 10.1093/jnci/92.3.205 1:STN:280:DC%2BD3c7it1Gitg%3D%3D
-
Therasse P, Arbuck SG, Eisenhauer EA, Wanders J, Kaplan RS, Rubinstein L, Verweij J, Van Glabbeke M, van Oosterom AT, Christian MC, Gwyther SG (2000) New guidelines to evaluate the response to treatment in solid tumors. European Organization for Research and Treatment of Cancer, National Cancer Institute of the United States, National Cancer Institute of Canada. J Natl Cancer Inst 92:205-216
-
(2000)
J Natl Cancer Inst
, vol.92
, pp. 205-216
-
-
Therasse, P.1
Arbuck, S.G.2
Eisenhauer, E.A.3
Wanders, J.4
Kaplan, R.S.5
Rubinstein, L.6
Verweij, J.7
Van Glabbeke, M.8
Van Oosterom, A.T.9
Christian, M.C.10
Gwyther, S.G.11
-
20
-
-
0027956791
-
Characterization of dextromethorphan N-demethylation by human liver microsomes. Contribution of the cytochrome P450 3A (CYP3A) subfamily
-
8043020 10.1016/0006-2952(94)90237-2 1:CAS:528:DyaK2cXlt1Cmt7w%3D
-
Gorski JC, Jones DR, Wrighton SA, Hall SD (1994) Characterization of dextromethorphan N-demethylation by human liver microsomes. Contribution of the cytochrome P450 3A (CYP3A) subfamily. Biochem Pharmacol 48:173-182
-
(1994)
Biochem Pharmacol
, vol.48
, pp. 173-182
-
-
Gorski, J.C.1
Jones, D.R.2
Wrighton, S.A.3
Hall, S.D.4
-
21
-
-
33846449874
-
Mechanism-based inactivation of human cytochrome p450 enzymes and the prediction of drug-drug interactions
-
17093004 10.1124/dmd.106.012633 1:CAS:528:DC%2BD2sXhvVKrs7k%3D
-
Obach RS, Walsky RL, Venkatakrishnan K (2007) Mechanism-based inactivation of human cytochrome p450 enzymes and the prediction of drug-drug interactions. Drug Metab Dispos 35:246-255
-
(2007)
Drug Metab Dispos
, vol.35
, pp. 246-255
-
-
Obach, R.S.1
Walsky, R.L.2
Venkatakrishnan, K.3
-
22
-
-
84865415281
-
-
U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER) Accessed 02/29 2012 Web site
-
U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER) (2012) Guidance for industry: Drug interaction studies-study design, data analysis, implications for dosing, and labeling recommendations. In: http://www.fda.gov Web site. http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/ Guidances/UCM292362.pdf. Accessed 02/29 2012
-
(2012)
Guidance for Industry: Drug Interaction Studies-study Design, Data Analysis, Implications for Dosing, and Labeling Recommendations
-
-
-
23
-
-
0029853347
-
The influence of CYP2D6 polymorphism and quinidine on the disposition and antitussive effect of dextromethorphan in humans
-
8841152 10.1016/S0009-9236(96)90056-9 1:CAS:528:DyaK28XmsFCrtLw%3D
-
Capon DA, Bochner F, Kerry N, Mikus G, Danz C, Somogyi AA (1996) The influence of CYP2D6 polymorphism and quinidine on the disposition and antitussive effect of dextromethorphan in humans. Clin Pharmacol Ther 60:295-307
-
(1996)
Clin Pharmacol Ther
, vol.60
, pp. 295-307
-
-
Capon, D.A.1
Bochner, F.2
Kerry, N.3
Mikus, G.4
Danz, C.5
Somogyi, A.A.6
-
24
-
-
0034782996
-
Comparative contribution to dextromethorphan metabolism by cytochrome P450 isoforms in vitro: Can dextromethorphan be used as a dual probe for both CTP2D6 and CYP3A activities?
-
11602530 1:CAS:528:DC%2BD3MXnsl2rs7k%3D
-
Yu A, Haining RL (2001) Comparative contribution to dextromethorphan metabolism by cytochrome P450 isoforms in vitro: can dextromethorphan be used as a dual probe for both CTP2D6 and CYP3A activities? Drug Metab Dispos 29:1514-1520
-
(2001)
Drug Metab Dispos
, vol.29
, pp. 1514-1520
-
-
Yu, A.1
Haining, R.L.2
-
25
-
-
51649126841
-
Histone deacetylase inhibitor panobinostat induces clinical responses with associated alterations in gene expression profiles in cutaneous T-cell lymphoma
-
18628465 10.1158/1078-0432.CCR-07-4262 1:CAS:528:DC%2BD1cXosFGitL0%3D
-
Ellis L, Pan Y, Smyth GK, George DJ, McCormack C, Williams-Truax R, Mita M, Beck J, Burris H, Ryan G, Atadja P, Butterfoss D, Dugan M, Culver K, Johnstone RW, Prince HM (2008) Histone deacetylase inhibitor panobinostat induces clinical responses with associated alterations in gene expression profiles in cutaneous T-cell lymphoma. Clin Cancer Res 14:4500-4510
-
(2008)
Clin Cancer Res
, vol.14
, pp. 4500-4510
-
-
Ellis, L.1
Pan, Y.2
Smyth, G.K.3
George, D.J.4
McCormack, C.5
Williams-Truax, R.6
Mita, M.7
Beck, J.8
Burris, H.9
Ryan, G.10
Atadja, P.11
Butterfoss, D.12
Dugan, M.13
Culver, K.14
Johnstone, R.W.15
Prince, H.M.16
-
26
-
-
84864024420
-
Panobinostat in patients with relapsed/refractory Hodgkin's lymphoma after autologous stem-cell transplantation: Results of a phase II study
-
22547596 10.1200/JCO.2011.38.1350 1:CAS:528:DC%2BC38XhtFCjtrnJ
-
Younes A, Sureda A, Ben-Yehuda D, Zinzani PL, Ong TC, Prince HM, Harrison SJ, Kirschbaum M, Johnston P, Gallagher J, Le Corre C, Shen A, Engert A (2012) Panobinostat in patients with relapsed/refractory Hodgkin's lymphoma after autologous stem-cell transplantation: results of a phase II study. J Clin Oncol 30:2197-2203
-
(2012)
J Clin Oncol
, vol.30
, pp. 2197-2203
-
-
Younes, A.1
Sureda, A.2
Ben-Yehuda, D.3
Zinzani, P.L.4
Ong, T.C.5
Prince, H.M.6
Harrison, S.J.7
Kirschbaum, M.8
Johnston, P.9
Gallagher, J.10
Le Corre, C.11
Shen, A.12
Engert, A.13
-
27
-
-
85081458379
-
-
U.S. Food and Drug Adminstration
-
U.S. Food and Drug Adminstration (2013) Drug Interactions & Labeling http://www.fda.gov/Drugs/DevelopmentApprovalProcess/DevelopmentResources/ DrugInteractionsLabeling/ucm080499.htm
-
(2013)
Drug Interactions & Labeling
-
-
|