Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Edward Piper"'
Autor:
Edward Piper, KKarin Bowen, Christopher E. Brightling, AnnaMaria Péterffy, Gene L. Colice, Reynold A. Panettieri, Ulf Sjöbring, Peter Wessman
Publikováno v:
The Lancet Respiratory Medicine. 6:511-525
Summary Background Tralokinumab is an anti-interleukin-13 human monoclonal antibody developed for the treatment of severe, uncontrolled asthma. These clinical trials aimed to assess the efficacy and safety of tralokinumab in this population. Methods
Autor:
Meena Jain, Piotr Kuna, Dewei She, Iwona Stelmach, Sara Sandbach, Paul Baverel, Balaji Agoram, Edward Piper
Publikováno v:
British Journal of Clinical Pharmacology. 80:1337-1349
Aims Tralokinumab, an investigational human immunoglobulin G4 monoclonal antibody, potently and specifically neutralizes interleukin-13, a central mediator of asthma. Tralokinumab has shown improvements in clinical endpoints in adults with uncontroll
Autor:
Katie Streicher, Stephanie Korn, Koustubh Ranade, Paul M. O'Byrne, Pascal Chanez, Edward Piper, Christopher E. Brightling, Dewei She, Richard Leigh, Richard D. May
Publikováno v:
The Lancet Respiratory Medicine. 3:692-701
Summary Background Interleukin 13 is a central mediator of asthma. Tralokinumab is a human interleukin-13 neutralising monoclonal antibody. We aimed to assess the efficacy and safety of two dosing regimens of tralokinumab in patients with severe unco
Autor:
Edward Piper, Gene L. Colice, Meena Jain, Göran Tornling, Martin Braddock, Dewei She, Lars H. Nordenmark, Christopher E. Brightling
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 194:118-120
Publikováno v:
Airway Pharmacology and Treatment.
Background: In a Phase 2b trial in patients with severe, uncontrolled asthma, the anti–Il-13 monoclonal antibody tralokinumab improved lung function and, in patients with increased baseline periostin and DPP-4, reduced asthma exacerbations [Lancet
Autor:
Dewei She, Hakop Gevorkyan, Raffaella Faggioni, Edward Piper, Tomoko Yoshioka, Shinya Ueda, Paul Baverel
Publikováno v:
Drug metabolism and pharmacokinetics. 33(3)
Tralokinumab is a human monoclonal antibody in clinical development for asthma and atopic dermatitis that specifically neutralizes interleukin-13. This phase I, single-blind, randomized, placebo-controlled, single ascending-dose study assessed the sa
Autor:
Richard M. Martin, Edward Piper, Chrisopher E. Brightling, Philip Brohawn, Gautam Damera, Dewei She, Inna Vainshtein, Meina Liang, Scott Martinez, Koustubh Ranade, Tuyet-Hang Pham, Katie Streicher, Fernanda Pilataxi, Michael Kuziora
Publikováno v:
5.1 Airway Pharmacology and Treatment.
RATIONALE: We sought biomarkers to identify asthma patients (pts) likely to benefit from tralokinumab, an anti–IL-13 IgG4 monoclonal antibody. METHODS: Airway epithelial cells grown in air-liquid interface cultures were stimulated with cytokines wi
Autor:
Nestor A. Molfino, Richard D. May, Gregory P. Geba, Chad K. Oh, Christopher E. Brightling, Edward Piper, Dewei She, Robert Niven, Kwai Poon, Chris Kell, Raffaella Faggioni
Publikováno v:
European Respiratory Journal. 41:330-338
Pre-clinical data demonstrate a pivotal role for interleukin (IL)-13 in the development and maintenance of asthma. This study assessed the effects of tralokinumab, an investigational human IL-13-neutralising immunoglobulin G4 monoclonal antibody, in
Autor:
Evan A. Stein, Harold E. Bays, Andrea H Spezzi, Jim Pedicano, Edward Piper, Dennis P. O'Brien
Publikováno v:
Circulation. 123:1974-1985
Background— Lapaquistat acetate is a squalene synthase inhibitor investigated for the treatment of hypercholesterolemia. Methods and Results— This report summarizes the phase 2 and 3 results from the lapaquistat clinical program, which was halted
Autor:
Martin Braddock, Gene L. Colice, Lars H. Nordenmark, Göran Tornling, Edward Piper, Meena Jain, Dewei She, Christopher E. Brightling
Publikováno v:
5.1 Airway Pharmacology and Treatment.
Introduction: The effects of the anti-IL-13 monoclonal antibody tralokinumab (tralo) (CAT-354) on airway dimensions were assessed in a subgroup of subjects from a Phase 2b study. Methods: In a 52-week double-blind study (NCT01402986) adults with seve