Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Bart Frederick"'
Autor:
Patrick Branigan, Zhenhua Xu, Ivo Nnane, Philipp Badorrek, Damien Fink, Donald Raible, Zhenling Yao, Karen E. Duffy, Maarten van den Boer, Cathye Shu, Bart Frederick, Tong-Yuan Yang, Frédéric Baribaud
Publikováno v:
Br J Clin Pharmacol
Aims To assess safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD) and immunogenicity of CNTO 7160, an anti-interleukin-33 receptor (IL-33R) monoclonal antibody, in healthy subjects and patients with asthma or atopic dermatitis (AD). M
Autor:
Tatiana Ort, Shannon Dogmanits, Ivo Nnane, Zhenling Yao, Fang Shen, Derrick E. Akpalu, Damien Fink, Donald Raible, Zhenhua Xu, Amarnath Sharma, Bart Frederick
Publikováno v:
Journal of clinical pharmacology. 59(7)
The safety, tolerability, pharmacokinetics, pharmacodynamics, and immunogenicity of JNJ-61178104, a novel anti-tumor necrosis factor-alpha (TNFα) and anti-interleukin-17A (IL-17A) bispecific antibody, were investigated in a placebo-controlled, first
Autor:
Joyce Ford, Bart Frederick, Joseph C. Marini, Manny Lopez, Chao Han, Dick E. de Vries, Stanley J. Marciniak, Chao Xu, Honghui Zhou, Rajesh Bandekar, Thomas A. Puchalski, Hugh M. Davis
Publikováno v:
Clinical Pharmacology in Drug Development. 3:328-334
Siltuximab, a monoclonal antibody (mAb) against interleukin (IL-6), is under development by Janssen Research & Development, LLC. During early clinical development, siltuximab was produced in a murine Sp2/0 myeloma cell line. The production cell line
Autor:
Zhenhua Xu, Craig Comisar, Hugh M. Davis, Bart Frederick, Joseph C. Marini, Bart van Hartingsveldt, Esther Bouman-Thio, Honghui Zhou
Publikováno v:
British Journal of Clinical Pharmacology. 72:270-281
AIMS To assess the safety, tolerability, pharmacokinetics (PK) and immunogenicity of sirukumab (CNTO 136) following intravenous (i.v.) infusion in healthy subjects.
Autor:
Bruce E. Miller, Adam F. Cohen, Stephen Bai, John Getsy, Esther Bouman-Thio, Jennifer Yohrling, Hugh M. Davis, Kari L. Franson, Haishan Jang, Bart Frederick, Stanley J. Marciniak, Jacobus Burggraaf, Qun Jiao
Publikováno v:
The Journal of Clinical Pharmacology. 48:1197-1207
The erythropoietin mimetic antibody fusion protein CNTO 528 was developed as a novel antibody fusion protein by constructing an active hematopoietic peptide onto an IgG1-based scaffold. This resulted in a molecule with a long circulating half-life an
Autor:
Gisela Torres, Eiko Toichi, Thomas S. McCormick, Kevin D. Cooper, Daniel E. Everitt, Mary Ann Mascelli, Bart Frederick, Catharine L. Kauffman, Timothy Chang, Charles Pendley, Nancy Aria, Alice B. Gottlieb
Publikováno v:
The Journal of Immunology. 177:4917-4926
Psoriasis is characterized by activation of T cells with a type 1 cytokine profile. IL-12 and IL-23 produced by APCs are essential for inducing Th1 effector cells. Promising clinical results of administration of an Ab specific for the p40 subunit of
Autor:
Bart Frederick, Daniel E. Everitt, Mary Ann Mascelli, Yaowei Zhu, Charles Pendley, Alice B. Gottlieb, Martin A. Graham, Kevin D. Cooper, Nancy Aria, Thomas S. McCormick, Eiko Toichi, Catharine L. Kauffman
Publikováno v:
Journal of Investigative Dermatology. 123:1037-1044
The potential therapeutic activity of a human monoclonal antibody to the human interleukin-12 p40 subunit (anti-IL-12p40) has been established both in vitro and in vivo, warranting a first-in-human investigation in psoriasis. This phase I, first-in-h
Autor:
John C. Pezzullo, Neal S. Kleiman, Bart Frederick, Darrell R. Abernethy, Jane E. Freedman, Mary Ann Mascelli
Publikováno v:
Clinical Pharmacology & Therapeutics. 71:186-195
Objectives Our objectives were to compare and contrast abciximab concentration-effect relationships in healthy volunteer participants with those in patients with coronary atherosclerosis undergoing elective coronary angioplasty. We also aimed to esta
Autor:
Bart Frederick, Elliot S. Barnathan, Mary Ann Mascelli, Robert E. Jordan, John C. Pezzullo, Jane E. Freedman, Darrell R. Abernethy
Publikováno v:
American Heart Journal. 143:87-94
Objective The purpose of the study was to establish a rebolus regimen for abciximab that restores pharmacologic glycoprotein (GP) IIb/IIIa receptor blockade within a short time frame (up to 48 hours) after completion of an initial treatment. Methods
Autor:
Zhenhua Xu, Honghui Zhou, Stanley J. Marciniak, Lilianne Kim, Yanli Zhuang, Bart Frederick, Hugh M. Davis
Publikováno v:
Clinical therapeutics. 37(2)
Purpose This Phase 1 pharmacokinetic (PK) comparability study in healthy subjects was performed to compare the PK properties and tolerability of single-dose golimumab 100 mg delivered subcutaneously by an autoinjector device or by a standard needle a