Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Donald Thornton"'
Autor:
Howard A. Fine, Paul S. Albert, Donald Thornton, Luna Musib, Jennifer Walling, Svetlana Kotliarova, Paul Duic, Kraig Moore, Lyndon Kim, Teri N. Kreisl
Purpose: Enzastaurin is a selective inhibitor of protein kinase C β. Prior phase I studies did not show increased drug exposures with escalating once daily administration. Limits from gastrointestinal absorption may be overcome by twice daily dosing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ba66e5356279b08adfdf4e1a9ed74d9
https://doi.org/10.1158/1078-0432.c.6516834.v1
https://doi.org/10.1158/1078-0432.c.6516834.v1
Autor:
Howard A. Fine, Paul S. Albert, Donald Thornton, Luna Musib, Jennifer Walling, Svetlana Kotliarova, Paul Duic, Kraig Moore, Lyndon Kim, Teri N. Kreisl
Supplementary Data from A Phase I Trial of Enzastaurin in Patients with Recurrent Gliomas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c59f4e7215f8bdd11cdb99ee355a3ab
https://doi.org/10.1158/1078-0432.22439349.v1
https://doi.org/10.1158/1078-0432.22439349.v1
Autor:
Michael Andreeff, Zhihong Zeng, Sergej Konoplev, Hong Mu, Byung Sik Cho, Sheng Bin Peng, Marina Protopopova, Joseph R. Marszalek, Marina Konopleva, Zhiqiang Wang, Donald Thornton, Wencai Ma, Teresa McQueen, Jorge E. Cortes, R. Eric Davis
Publikováno v:
Blood. 126:222-232
Targeting the stromal cell-derived factor 1α (SDF-1α)/C-X-C chemokine receptor type 4 (CXCR4) axis has been shown to be a promising therapeutic approach to overcome chemoresistance in acute myeloid leukemia (AML). We investigated the antileukemia e
Publikováno v:
Cancer Research. 76:OT1-03
Background: Abemaciclib, an oral drug administered twice daily on a continuous schedule, is an inhibitor of both CDK4 and CDK6. In study JPBA, abemaciclib demonstrated evidence of single-agent activity in a cohort of patients with heavily pretreated
A Phase 1 Study of LY2874455, an Oral Selective pan-FGFR Inhibitor, in Patients with Advanced Cancer
Autor:
Young Suk Park, Jeanne Tie, Donald Thornton, Eyas Raddad, Yung-Jue Bang, Michael Michael, Sonya C. Tate, Tae Min Kim, Oday Hamid, Yoon-Koo Kang
Publikováno v:
Targeted oncology. 12(4)
We report here a phase 1 study of LY2874455, a potent oral selective pan-fibroblast growth factor receptor (FGFR) inhibitor. The primary objective was to determine the recommended phase 2 dosing (RP2D). Secondary objectives included determining toxic
Autor:
John R. Stille, Eyas Raddad, John Polzer, Matthew D. Galsky, Stephanie Roberson, Paul Conkling, Nicholas J. Vogelzang, Mansoor N. Saleh, Donald Thornton
Publikováno v:
Clinical Cancer Research. 20:3581-3588
Purpose: Overexpression of C-X-C motif receptor 4 (CXCR4) is implicated in tumor progression. LY2510924 is a peptide antagonist, which blocks stromal cell–derived factor-1 (SDF1) from CXCR4 binding. Experimental Design: This phase I study included
Autor:
Sabine Ermisch, Ting Wang, Michael A. Carducci, Jeannette Day, Deborah K. Armstrong, Lori Kornberg, Rodney Decker, Connie Collins, Steven J. Nicol, Donald Thornton, Lee P. Resta, Zhe Zhang, Nwabundo Nwankwo
Publikováno v:
Investigational New Drugs
Summary Purpose Given distinct mechanism of actions of enzastaurin and bevacizumab, preclinical studies suggest enhanced antitumor activity in combination. This phase I study assessed the combination’s safety and efficacy. Patients and methods Six
Autor:
Paul S. Albert, John A. Butman, Howard A. Fine, Svetlana Kotliarova, Teri N. Kreisl, Lyndon Kim, Donald Thornton, Luna Musib
Publikováno v:
Neuro-Oncology. 12:181-189
Enzastaurin, a potent inhibitor of protein kinase C-beta, inhibits angiogenesis and has direct cytotoxic activity against glioma cells in preclinical studies. Patients with recurrent high-grade gliomas were stratified by histology and use of enzyme-i
Autor:
Nathan Enas, Kerry J. Savage, Donald Thornton, Stuart L. Goldberg, Brad S. Kahl, Margaret A. Shipp, Christelle Darstein, Donna Neuberg, Patrick Flynn, Jon C. Aster, Ann S. LaCasce, Michael J. Robertson, Sven De Vos, Luna Musib, Kendrith M Rowland, Julie M. Vose, Jose C. Cruz, Jeffery L. Kutok, Mary Laughlin, Christopher A. Slapak
Publikováno v:
Journal of Clinical Oncology. 25:1741-1746
Purpose Protein kinase C beta (PKCβ) was identified by gene-expression profiling, preclinical evaluation, and independent immunohistochemical analysis as a rational therapeutic target in diffuse large B-cell lymphoma (DLBCL). We conducted a multicen
Publikováno v:
Journal of Clinical Oncology. 35:TPS4150-TPS4150
TPS4150 Background: PDAC is a lethal tumor with unusual resistance to cytotoxic and targeted therapies, and pathogenesis frequently associated with hyperactive CDK 4&6 signaling. Pre-clinical models have demonstrated anti-proliferative activity with