Development and validation of an UPLC-MS/MS method for quantitative analysis of OTX015 in human plasma samples
Author:
Affiliation:
1. RadioPharmacology Department
2. Curie Institute-René Huguenin Hospital
3. 92210 Saint-Cloud, France
4. Oncology Therapeutic Development
5. 92110 Clichy, France
6. Oncoethix SA
7. CH-1006 Lausanne, Switzerland
Abstract
Development and validation of a rapid and robust UPLC-MS/MS method for quantification of a novel bromodomain inhibitor, OTX015 and its application to a pharmacokinetic study.
Publisher
Royal Society of Chemistry (RSC)
Subject
General Engineering,General Chemical Engineering,Analytical Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2014/AY/C4AY02249A
Reference21 articles.
1. Crystal Structure of the Human BRD2 Bromodomain
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4. Targeting MYC dependence in cancer by inhibiting BET bromodomains
5. BET Bromodomain Inhibition as a Therapeutic Strategy to Target c-Myc
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1. Insights into the cellular pharmacological properties of the BET-inhibitor OTX015/MK-8628 (birabresib), alone and in combination, in leukemia models;Leukemia & Lymphoma;2019-06-17
2. Phase Ib Trial With Birabresib, a Small-Molecule Inhibitor of Bromodomain and Extraterminal Proteins, in Patients With Selected Advanced Solid Tumors;Journal of Clinical Oncology;2018-10-20
3. The bromodomain inhibitor OTX015 (MK-8628) exerts anti-tumor activity in triple-negative breast cancer models as single agent and in combination with everolimus;Oncotarget;2016-12-07
4. Bromodomain inhibitor OTX015 (MK-8628) combined with targeted agents shows strong in vivo antitumor activity in lymphoma;Oncotarget;2016-08-01
5. OTX015 (MK-8628), a novel BET inhibitor, displaysin vitroandin vivoantitumor effects alone and in combination with conventional therapies in glioblastoma models;International Journal of Cancer;2016-07-30
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