Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Jagdev S. Sidhu"'
Autor:
Timothy J. Craig, Jagdev S. Sidhu, Ingo Pragst, Dipti Pawaskar, Michael A. Tortorici, Bruce L. Zuraw, Marco Cicardi, Thomas Machnig, Matthew Hutmacher, Hilary Longhurst, Ying Zhang
Publikováno v:
CPT: Pharmacometrics & Systems Pharmacology. 7:158-165
Subcutaneous C1-inhibitor (HAEGARDA, CSL Behring), is a US Food and Drug Administration (FDA)-approved, highly concentrated formulation of a plasma-derived C1-esterase inhibitor (C1-INH), which, in the phase III Clinical Studies for Optimal Managemen
Autor:
Alex Veldman, Ying Zhang, John Roberts, Jagdev S. Sidhu, Michael A. Tortorici, Annette Feussner, K. St. Ledger
Publikováno v:
Journal of Thrombosis and Haemostasis. 15:1106-1114
Essentials rVIII-SingleChain is a unique recombinant factor VIII (FVIII) molecule. A population pharmacokinetic model was based on FVIII activity of severe hemophilia A patients. The model was used to simulate factor VIII activity–time profiles for
Autor:
T. Yuraszeck, W. Seifert, Jagdev S. Sidhu, Elena Santagostino, Ying Zhang, Annette Feussner, W. McKeand
Publikováno v:
Science meets clinical practice.
Autor:
H. Henry Li, Paul K. Keith, Michael A. Tortorici, Bruce L. Zuraw, Inmaculada Martinez-Saguer, Hilary Longhurst, Jagdev S. Sidhu, Timothy J. Craig, Constance H. Katelaris, Jonathan A. Bernstein, Joshua J. Jacobs, Marc A. Riedl, William R. Lumry, Marco Cicardi, Annette Feussner, Dipti Pawaskar
Publikováno v:
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology. 48(10)
Background Long-term prophylaxis with subcutaneous (SC) administration of a highly concentrated plasma-derived C1-esterase inhibitor (C1-INH) formulation was recently approved by the Food and Drug Administration for hereditary angioedema (HAE) attack
Autor:
Jonathan A. Bernstein, Inmaculada Martinez-Saguer, Hilary Longhurst, Henrike Feuersenger, R. Parasrampuria, Huamin Henry Li, Marco Cicardi, Bruce L. Zuraw, Jonathan M. Edelman, Timothy J. Craig, Petra Staubach, Syed M. Rehman, Markus Magerl, Jagdev S. Sidhu
Publikováno v:
Allergy
Background Hereditary angioedema (HAE) due to C1 inhibitor deficiency manifests as recurrent swelling attacks that can be disabling and sometimes fatal. Long‐term prophylaxis with twice‐weekly intravenous injections of plasma‐derived C1‐inhib
Publikováno v:
Biologics in Therapy
Introduction Standard treatment for patients with primary immunodeficiency (PID) is monthly intravenous immunoglobulin (IVIG), or weekly/biweekly subcutaneous immunoglobulin (SCIG) infusion. We used population pharmacokinetic modeling to predict immu
Autor:
Carl M. J. Kirkpatrick, Martin Bexon, Jianfeng Lu, Mikhail Rojavin, Jonathan M. Edelman, Cornelia B. Landersdorfer, Jagdev S. Sidhu, Mark Pfister
Publikováno v:
Postgraduate Medicine. 125:53-61
Replacement therapy with immunoglobulin G (IgG) given as intravenous or subcutaneous (SC) infusions is the standard treatment for patients with primary immunodeficiency. Due to the life-long need for replacement, increased flexibility in the administ
Autor:
John Roberts, Elena Santagostino, Christine Voigt, Massimo Morfini, Debra M. Bensen-Kennedy, Ying Zhang, Jagdev S. Sidhu, Annette Feussner, Iris Jacobs
Publikováno v:
Journal of thrombosis and haemostasis : JTH. 14(11)
Essentials The new recombinant factor IX (FIX) albumin fusion protein (rIX-FP) has a prolonged half-life. A population pharmacokinetic (PK) model was based on FIX activity levels of hemophilia B patients. The model was used to simulate different dosi
Publikováno v:
Clinical & Experimental Immunology. 178:146-148
Immunoglobulin (Ig)G therapy is the primary treatment for patients with primary antibody deficiencies (PAD), and can be administered intravenously [intravenous immunoglobulin (IVIg)] or subcutaneously [subcutaneous immunoglobulin (SCIg)]. IVIg has be
Autor:
Michael Ashton, Jagdev S. Sidhu
Publikováno v:
The American Journal of Tropical Medicine and Hygiene. 56:13-16
A comparison of venous plasma, capillary plasma, and saliva pharmacokinetics of artemisinin was performed in four healthy subjects given a single 500 mg dose. Artemisinin was determined to be 88% bound in venous plasma. Saliva levels were more closel