These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
147 related articles for article (PubMed ID: 28353123)
1. A phase 1, open label, dose escalation study to investigate the safety, tolerability, and pharmacokinetics of MG1102 (apolipoprotein(a) Kringle V) in patients with solid tumors. Kim GM; Reid T; Shin SJ; Rha SY; Ahn JB; Lee SS; Chung HC Invest New Drugs; 2017 Dec; 35(6):773-781. PubMed ID: 28353123 [TBL] [Abstract][Full Text] [Related]
2. Phase 1, open-label, dose escalation, safety, and pharmacokinetics study of ME-344 as a single agent in patients with refractory solid tumors. Bendell JC; Patel MR; Infante JR; Kurkjian CD; Jones SF; Pant S; Burris HA; Moreno O; Esquibel V; Levin W; Moore KN Cancer; 2015 Apr; 121(7):1056-63. PubMed ID: 25411085 [TBL] [Abstract][Full Text] [Related]
3. A phase I dose-escalation study of Tivantinib (ARQ 197) in adult patients with metastatic solid tumors. Rosen LS; Senzer N; Mekhail T; Ganapathi R; Chai F; Savage RE; Waghorne C; Abbadessa G; Schwartz B; Dreicer R Clin Cancer Res; 2011 Dec; 17(24):7754-64. PubMed ID: 21976535 [TBL] [Abstract][Full Text] [Related]
4. A phase I trial to determine the safety, pharmacokinetics, and pharmacodynamics of intercalated BMS-690514 with paclitaxel/carboplatin (PC) in advanced or metastatic solid malignancies. Chow LQ; Jonker DI; Dy GK; Nicholas G; Fortin C; Patricia D; Adjei AA; Belani CP; Gupta A; Park JS; Zhang S; Sbar EI; Laurie SA Cancer Chemother Pharmacol; 2013 May; 71(5):1273-85. PubMed ID: 23468081 [TBL] [Abstract][Full Text] [Related]
5. Phase I dose-escalation study of the safety, pharmacokinetics, and pharmacodynamics of the MEK inhibitor RO4987655 (CH4987655) in patients with advanced solid tumors. Leijen S; Middleton MR; Tresca P; Kraeber-Bodéré F; Dieras V; Scheulen ME; Gupta A; Lopez-Valverde V; Xu ZX; Rueger R; Tessier JJ; Shochat E; Blotner S; Naegelen VM; Schellens JH; Eberhardt WE Clin Cancer Res; 2012 Sep; 18(17):4794-805. PubMed ID: 22767668 [TBL] [Abstract][Full Text] [Related]
6. Safety and activity of RRx-001 in patients with advanced cancer: a first-in-human, open-label, dose-escalation phase 1 study. Reid T; Oronsky B; Scicinski J; Scribner CL; Knox SJ; Ning S; Peehl DM; Korn R; Stirn M; Carter CA; Oronsky A; Taylor MJ; Fitch WL; Cabrales P; Kim MM; Burris HA; Lao CD; Abrouk NED; Fanger GR; Infante JR Lancet Oncol; 2015 Sep; 16(9):1133-1142. PubMed ID: 26296952 [TBL] [Abstract][Full Text] [Related]
7. Phase I Study of OPB-31121, an Oral STAT3 Inhibitor, in Patients with Advanced Solid Tumors. Oh DY; Lee SH; Han SW; Kim MJ; Kim TM; Kim TY; Heo DS; Yuasa M; Yanagihara Y; Bang YJ Cancer Res Treat; 2015 Oct; 47(4):607-15. PubMed ID: 25715763 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Safety, pharmacokinetic, and pharmacodynamic phase I dose-escalation trial of PF-00562271, an inhibitor of focal adhesion kinase, in advanced solid tumors. Infante JR; Camidge DR; Mileshkin LR; Chen EX; Hicks RJ; Rischin D; Fingert H; Pierce KJ; Xu H; Roberts WG; Shreeve SM; Burris HA; Siu LL J Clin Oncol; 2012 May; 30(13):1527-33. PubMed ID: 22454420 [TBL] [Abstract][Full Text] [Related]
10. First-in-human, phase I dose-escalation study of the safety, pharmacokinetics, and pharmacodynamics of RO5126766, a first-in-class dual MEK/RAF inhibitor in patients with solid tumors. Martinez-Garcia M; Banerji U; Albanell J; Bahleda R; Dolly S; Kraeber-Bodéré F; Rojo F; Routier E; Guarin E; Xu ZX; Rueger R; Tessier JJ; Shochat E; Blotner S; Naegelen VM; Soria JC Clin Cancer Res; 2012 Sep; 18(17):4806-19. PubMed ID: 22761467 [TBL] [Abstract][Full Text] [Related]
11. Oral administration of irinotecan in patients with solid tumors: an open-label, phase I, dose escalating study evaluating safety, tolerability and pharmacokinetics. Kümler I; Sørensen PG; Palshof J; Høgdall E; Skovrider-Ruminski W; Theile S; Fullerton A; Nielsen PG; Jensen BV; Nielsen DL Cancer Chemother Pharmacol; 2019 Jan; 83(1):169-178. PubMed ID: 30406838 [TBL] [Abstract][Full Text] [Related]
12. A phase I dose-escalation study of MEDI-575, a PDGFRα monoclonal antibody, in adults with advanced solid tumors. Becerra CR; Conkling P; Vogelzang N; Wu H; Hong S; Narwal R; Liang M; Tavakkoli F; Pandya N Cancer Chemother Pharmacol; 2014 Nov; 74(5):917-25. PubMed ID: 25149088 [TBL] [Abstract][Full Text] [Related]
13. Safety, pharmacokinetics, and pharmacodynamics of AMG 102, a fully human hepatocyte growth factor-neutralizing monoclonal antibody, in a first-in-human study of patients with advanced solid tumors. Gordon MS; Sweeney CS; Mendelson DS; Eckhardt SG; Anderson A; Beaupre DM; Branstetter D; Burgess TL; Coxon A; Deng H; Kaplan-Lefko P; Leitch IM; Oliner KS; Yan L; Zhu M; Gore L Clin Cancer Res; 2010 Jan; 16(2):699-710. PubMed ID: 20068101 [TBL] [Abstract][Full Text] [Related]
14. First-in-man dose escalation and pharmacokinetic study of CAP7.1, a novel prodrug of etoposide, in adults with refractory solid tumours. Keilholz U; Rohde L; Mehlitz P; Knoedler M; Schmittel A; Kümmerlen V; Klinghammer K; Treasure P; Lassus M; Steventon G; Machacek M; Utku N Eur J Cancer; 2017 Jul; 80():14-25. PubMed ID: 28531881 [TBL] [Abstract][Full Text] [Related]
15. Phase I, dose-escalation study of BKM120, an oral pan-Class I PI3K inhibitor, in patients with advanced solid tumors. Bendell JC; Rodon J; Burris HA; de Jonge M; Verweij J; Birle D; Demanse D; De Buck SS; Ru QC; Peters M; Goldbrunner M; Baselga J J Clin Oncol; 2012 Jan; 30(3):282-90. PubMed ID: 22162589 [TBL] [Abstract][Full Text] [Related]
16. Phase I Dose-Escalation Study of the Multikinase Inhibitor Lenvatinib in Patients with Advanced Solid Tumors and in an Expanded Cohort of Patients with Melanoma. Hong DS; Kurzrock R; Wheler JJ; Naing A; Falchook GS; Fu S; Kim KB; Davies MA; Nguyen LM; George GC; Xu L; Shumaker R; Ren M; Mink J; Bedell C; Andresen C; Sachdev P; O'Brien JP; Nemunaitis J Clin Cancer Res; 2015 Nov; 21(21):4801-10. PubMed ID: 26169970 [TBL] [Abstract][Full Text] [Related]
17. Phase I Dose-Escalation Study of Ramucirumab in Chinese Patients with Advanced Solid Tumors. Cao J; Ji D; Chen Z; Shen W; Wang J; Li B; Chi H; Long A; Gao L; Li J Oncologist; 2017 Jun; 22(6):638-e56. PubMed ID: 28465370 [TBL] [Abstract][Full Text] [Related]
18. Phase I and pharmacokinetic/pharmacodynamic study of RO5126766, a first-in-class dual Raf/MEK inhibitor, in Japanese patients with advanced solid tumors. Honda K; Yamamoto N; Nokihara H; Tamura Y; Asahina H; Yamada Y; Suzuki S; Yamazaki N; Ogita Y; Tamura T Cancer Chemother Pharmacol; 2013 Sep; 72(3):577-84. PubMed ID: 23860959 [TBL] [Abstract][Full Text] [Related]
19. Phase I dose-escalation study of MEDI-573, a bispecific, antiligand monoclonal antibody against IGFI and IGFII, in patients with advanced solid tumors. Haluska P; Menefee M; Plimack ER; Rosenberg J; Northfelt D; LaVallee T; Shi L; Yu XQ; Burke P; Huang J; Viner J; McDevitt J; LoRusso P Clin Cancer Res; 2014 Sep; 20(18):4747-57. PubMed ID: 25024259 [TBL] [Abstract][Full Text] [Related]
20. A phase 1 dose escalation study of BI 831266, an inhibitor of Aurora kinase B, in patients with advanced solid tumors. Dittrich C; Fridrik MA; Koenigsberg R; Lee C; Goeldner RG; Hilbert J; Greil R Invest New Drugs; 2015 Apr; 33(2):409-22. PubMed ID: 25529193 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]