104 related articles for article (PubMed ID: 25947566)
1. First-in-human, phase I study of elisidepsin (PM02734) administered as a 30-min or as a 3-hour intravenous infusion every three weeks in patients with advanced solid tumors.
Ratain MJ; Geary D; Undevia SD; Coronado C; Alfaro V; Iglesias JL; Schilsky RL; Miguel-Lillo B
Invest New Drugs; 2015 Aug; 33(4):901-10. PubMed ID: 25947566
[TBL] [Abstract][Full Text] [Related]
2. A phase I and pharmacokinetic study of elisidepsin (PM02734) in patients with advanced solid tumors.
Salazar R; Jones RJ; Oaknin A; Crawford D; Cuadra C; Hopkins C; Gil M; Coronado C; Soto-Matos A; Cullell-Young M; Iglesias Dios JL; Evans TR
Cancer Chemother Pharmacol; 2012 Nov; 70(5):673-81. PubMed ID: 22926637
[TBL] [Abstract][Full Text] [Related]
3. Phase Ib/II study of elisidepsin in metastatic or advanced gastroesophageal cancer (IMAGE trial).
Petty R; Anthoney A; Metges JP; Alsina M; Gonçalves A; Brown J; Montagut C; Gunzer K; Laus G; Iglesias Dios JL; Miguel-Lillo B; Bohan P; Salazar R
Cancer Chemother Pharmacol; 2016 Apr; 77(4):819-27. PubMed ID: 26964995
[TBL] [Abstract][Full Text] [Related]
4. Phase I study of weekly kahalalide F as prolonged infusion in patients with advanced solid tumors.
Salazar R; Cortés-Funes H; Casado E; Pardo B; López-Martín A; Cuadra C; Tabernero J; Coronado C; García M; Soto Matos-Pita A; Miguel-Lillo B; Cullell-Young M; Iglesias Dios JL; Paz-Ares L
Cancer Chemother Pharmacol; 2013 Jul; 72(1):75-83. PubMed ID: 23645288
[TBL] [Abstract][Full Text] [Related]
5. Phase I, dose-escalating study of elisidepsin (Irvalec(®)), a plasma membrane-disrupting marine antitumor agent, in combination with erlotinib in patients with advanced malignant solid tumors.
Goel S; Viteri S; Morán T; Coronado C; Dios JL; Miguel-Lillo B; Fernández-García EM; Rosell R
Invest New Drugs; 2016 Feb; 34(1):75-83. PubMed ID: 26627080
[TBL] [Abstract][Full Text] [Related]
6. A phase I pharmacokinetic study of PM00104 (Zalypsis) administered as a 24-h intravenous infusion every 3 weeks in patients with advanced solid tumors.
Capdevila J; Clive S; Casado E; Michie C; Piera A; Sicart E; Carreras MJ; Coronado C; Kahatt C; Soto Matos-Pita A; Fernandez Teruel C; Siguero M; Cullell-Young M; Tabernero J
Cancer Chemother Pharmacol; 2013 May; 71(5):1247-54. PubMed ID: 23455428
[TBL] [Abstract][Full Text] [Related]
7. Phase I study of elisidepsin (Irvalec®) in combination with carboplatin or gemcitabine in patients with advanced malignancies.
Goldwasser F; Faivre S; Alexandre J; Coronado C; Fernández-García EM; Kahatt CM; Paramio PG; Dios JL; Miguel-Lillo B; Raymond E
Invest New Drugs; 2014 Jun; 32(3):500-9. PubMed ID: 24395456
[TBL] [Abstract][Full Text] [Related]
8. Phase I clinical and pharmacokinetic study of plitidepsin as a 1-hour weekly intravenous infusion in patients with advanced solid tumors.
Izquierdo MA; Bowman A; García M; Jodrell D; Martinez M; Pardo B; Gómez J; López-Martin JA; Jimeno J; Germá JR; Smyth JF
Clin Cancer Res; 2008 May; 14(10):3105-12. PubMed ID: 18483378
[TBL] [Abstract][Full Text] [Related]
9. Phase I study of depsipeptide in pediatric patients with refractory solid tumors: a Children's Oncology Group report.
; Fouladi M; Furman WL; Chin T; Freeman BB; Dudkin L; Stewart CF; Krailo MD; Speights R; Ingle AM; Houghton PJ; Wright J; Adamson PC; Blaney SM
J Clin Oncol; 2006 Aug; 24(22):3678-85. PubMed ID: 16877737
[TBL] [Abstract][Full Text] [Related]
10. Phase I clinical and pharmacokinetic study of kahalalide F administered weekly as a 1-hour infusion to patients with advanced solid tumors.
Pardo B; Paz-Ares L; Tabernero J; Ciruelos E; García M; Salazar R; López A; Blanco M; Nieto A; Jimeno J; Izquierdo MA; Trigo JM
Clin Cancer Res; 2008 Feb; 14(4):1116-23. PubMed ID: 18281545
[TBL] [Abstract][Full Text] [Related]
11. Phase I study of PM00104 (Zalypsis®) administered as a 1-hour weekly infusion resting every fourth week in patients with advanced solid tumors.
Massard C; Margetts J; Amellal N; Drew Y; Bahleda R; Stephens P; Armand JP; Calvert H; Soria JC; Coronado C; Kahatt C; Alfaro V; Siguero M; Fernández-Teruel C; Plummer R
Invest New Drugs; 2013 Jun; 31(3):623-30. PubMed ID: 22688291
[TBL] [Abstract][Full Text] [Related]
12. Phase I study of Aplidine in a dailyx5 one-hour infusion every 3 weeks in patients with solid tumors refractory to standard therapy. A National Cancer Institute of Canada Clinical Trials Group study: NCIC CTG IND 115.
Maroun JA; Belanger K; Seymour L; Matthews S; Roach J; Dionne J; Soulieres D; Stewart D; Goel R; Charpentier D; Goss G; Tomiak E; Yau J; Jimeno J; Chiritescu G;
Ann Oncol; 2006 Sep; 17(9):1371-8. PubMed ID: 16966366
[TBL] [Abstract][Full Text] [Related]
13. First-in-human phase I study of Lurbinectedin (PM01183) in patients with advanced solid tumors.
Elez ME; Tabernero J; Geary D; Macarulla T; Kang SP; Kahatt C; Pita AS; Teruel CF; Siguero M; Cullell-Young M; Szyldergemajn S; Ratain MJ
Clin Cancer Res; 2014 Apr; 20(8):2205-14. PubMed ID: 24563480
[TBL] [Abstract][Full Text] [Related]
14. Phase I clinical trial and pharmacokinetic study of the spicamycin analog KRN5500 administered as a 1-hour intravenous infusion for five consecutive days to patients with refractory solid tumors.
Supko JG; Eder JP; Ryan DP; Seiden MV; Lynch TJ; Amrein PC; Kufe DW; Clark JW
Clin Cancer Res; 2003 Nov; 9(14):5178-86. PubMed ID: 14613997
[TBL] [Abstract][Full Text] [Related]
15. Phase I and pharmacokinetic study of triapine, a potent ribonucleotide reductase inhibitor, administered daily for five days in patients with advanced solid tumors.
Murren J; Modiano M; Clairmont C; Lambert P; Savaraj N; Doyle T; Sznol M
Clin Cancer Res; 2003 Sep; 9(11):4092-100. PubMed ID: 14519631
[TBL] [Abstract][Full Text] [Related]
16. Phase I first-in-human study of CUDC-101, a multitargeted inhibitor of HDACs, EGFR, and HER2 in patients with advanced solid tumors.
Shimizu T; LoRusso PM; Papadopoulos KP; Patnaik A; Beeram M; Smith LS; Rasco DW; Mays TA; Chambers G; Ma A; Wang J; Laliberte R; Voi M; Tolcher AW
Clin Cancer Res; 2014 Oct; 20(19):5032-40. PubMed ID: 25107918
[TBL] [Abstract][Full Text] [Related]
17. Oral topotecan given once or twice daily for ten days: a phase I pharmacology study in adult patients with solid tumors.
Gerrits CJ; Burris H; Schellens JH; Eckardt JR; Planting AS; van der Burg ME; Rodriguez GI; Loos WJ; van Beurden V; Hudson I; Fields S; Von Hoff DD; Verweij J
Clin Cancer Res; 1998 May; 4(5):1153-8. PubMed ID: 9607572
[TBL] [Abstract][Full Text] [Related]
18. Phase I and pharmacokinetic study of aplidine, a new marine cyclodepsipeptide in patients with advanced malignancies.
Faivre S; Chièze S; Delbaldo C; Ady-Vago N; Guzman C; Lopez-Lazaro L; Lozahic S; Jimeno J; Pico F; Armand JP; Martin JA; Raymond E
J Clin Oncol; 2005 Nov; 23(31):7871-80. PubMed ID: 16172454
[TBL] [Abstract][Full Text] [Related]
19. First-in-man phase I trial of two schedules of the novel synthetic tetrahydroisoquinoline alkaloid PM00104 (Zalypsis) in patients with advanced solid tumours.
Yap TA; Cortes-Funes H; Shaw H; Rodriguez R; Olmos D; Lal R; Fong PC; Tan DS; Harris D; Capdevila J; Coronado C; Alfaro V; Soto-Matos A; Fernández-Teruel C; Siguero M; Tabernero JM; Paz-Ares L; de Bono JS; López-Martin JA
Br J Cancer; 2012 Apr; 106(8):1379-85. PubMed ID: 22491421
[TBL] [Abstract][Full Text] [Related]
20. Phase I and pharmacokinetic study of exatecan mesylate (DX-8951f): a novel camptothecin analog.
Royce ME; Hoff PM; Dumas P; Lassere Y; Lee JJ; Coyle J; Ducharme MP; De Jager R; Pazdur R
J Clin Oncol; 2001 Mar; 19(5):1493-500. PubMed ID: 11230496
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
