Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Aditi R. Saxena"'
Autor:
John D. Groarke, Jeffrey Crawford, Susie M. Collins, Shannon L. Lubaczewski, Danna M. Breen, Magdalena A. Harrington, Ira Jacobs, Ruolun Qiu, James Revkin, Michelle I. Rossulek, Aditi R. Saxena
Publikováno v:
Journal of Cachexia, Sarcopenia and Muscle, Vol 15, Iss 3, Pp 1054-1061 (2024)
Abstract Background Cancer cachexia is a multifactorial metabolic wasting syndrome characterized by anorexia, unintentional loss of weight involving both skeletal muscle and adipose tissues, progressive functional impairment and reduced survival. The
Externí odkaz:
https://doaj.org/article/43771e5cd792467db7f7100408a7e000
Publikováno v:
Obesity Science & Practice, Vol 7, Iss 3, Pp 281-290 (2021)
Abstract Background and Objective Obesity is a chronic disease associated with many serious comorbidities. Pharmacologic therapies are approved for the treatment of obesity; however, short‐term biomarkers to predict weight loss are not well underst
Externí odkaz:
https://doaj.org/article/44f51b6e1dc943ccb5c5f3aaa9647ee7
Autor:
Aditi R. Saxena, Stephanie‐An Lyle, Kaivan Khavandi, Ruolun Qiu, Mark Whitlock, William P. Esler, Albert M. Kim
Publikováno v:
Diabetes, Obesity and Metabolism. 25:992-1001
Publikováno v:
Clinical Therapeutics. 45:55-70
Autor:
Ryosuke Ono, Kenichi Furihata, Yoshihiko Ichikawa, Yoshiomi Nakazuru, Arthur Bergman, Donal N. Gorman, Aditi R. Saxena
Publikováno v:
Diabetes, Obesity and Metabolism. 25:805-814
Autor:
Aditi R, Saxena, Stephanie-An, Lyle, Kaivan, Khavandi, Ruolun, Qiu, Mark, Whitlock, William P, Esler, Albert M, Kim
Publikováno v:
Diabetes, obesitymetabolism.
To assess the safety, tolerability, and pharmacodynamics (PD) of ketohexokinase inhibitor PF-06835919 in participants with nonalcoholic fatty liver disease (NAFLD) and type 2 diabetes mellitus (T2DM).This double-blind, placebo-controlled, parallel-gr
Autor:
Ryosuke, Ono, Kenichi, Furihata, Yoshihiko, Ichikawa, Yoshiomi, Nakazuru, Arthur, Bergman, Donal N, Gorman, Aditi R, Saxena
Publikováno v:
Diabetes, obesitymetabolismREFERENCES.
This study investigated the safety, tolerability, pharmacokinetics and pharmacodynamics of danuglipron (PF-06882961), which is a novel, oral small-molecule glucagon-like peptide-1 receptor agonist, in Japanese participants with type 2 diabetes mellit
Autor:
Arthur Bergman, Kristin Chidsey, Aditi R. Saxena, Ryan M. Esquejo, Donal Gorman, Albert M. Kim, David A. Griffith, Clare Buckeridge
Publikováno v:
Nature Medicine. 27:1079-1087
Agonism of the glucagon-like peptide-1 receptor (GLP-1R) results in glycemic lowering and body weight loss and is a therapeutic strategy to treat type 2 diabetes (T2D) and obesity. We developed danuglipron (PF-06882961), an oral small-molecule GLP-1R
Autor:
David A. Griffith, David J. Edmonds, Jean-Philippe Fortin, Amit S. Kalgutkar, J. Brent Kuzmiski, Paula M. Loria, Aditi R. Saxena, Scott W. Bagley, Clare Buckeridge, John M. Curto, David R. Derksen, João M. Dias, Matthew C. Griffor, Seungil Han, V. Margaret Jackson, Margaret S. Landis, Daniel Lettiere, Chris Limberakis, Yuhang Liu, Alan M. Mathiowetz, Jayesh C. Patel, David W. Piotrowski, David A. Price, Roger B. Ruggeri, David A. Tess
Publikováno v:
Journal of medicinal chemistry. 65(12)
Peptide agonists of the glucagon-like peptide-1 receptor (GLP-1R) have revolutionized diabetes therapy, but their use has been limited because they require injection. Herein, we describe the discovery of the orally bioavailable, small-molecule, GLP-1
Autor:
RYOSUKE ONO, KENICHI FURIHATA, YOSHIHIKO ICHIKAWA, YOSHIOMI NAKAZURU, ARTHUR BERGMAN, DONAL N. GORMAN, ADITI R. SAXENA
Publikováno v:
Diabetes. 71
Danuglipron is an oral small molecule glucagon-like peptide-1 receptor (GLP-1R) agonist shown to reduce plasma glucose and body weight after 28 days of treatment in adults with type 2 diabetes mellitus (T2DM) . This randomized, double-blind (sponsor-