Jon H. Condra - Doylestown PA, US Rose M. Cubbon - Fanwood NJ, US Holly A. Hammond - Telford PA, US Timothy McCabe - Doylestown PA, US Shilpa Pandit - Edison NJ, US Laurence B. Peterson - Westfield NJ, US Joseph C. Santoro - Belle Mead NJ, US Ayesha Sitlani - Metuchen NJ, US Dana D. Wood - Collegeville PA, US Henryk Mach - Ambler PA, US Heidi Yoder - Glenside PA, US Sonia M. Gregory - Blue Bell PA, US Jeffrey T. Blue - Telford PA, US Kevin Wang - Lansdale PA, US Peter Luo - Lansdale PA, US Denise K. Nawrocki - Annandale NJ, US Pingyu Zhong - Blue Bell PA, US Feng Dong - Lansdale PA, US Yan Li - San Jose CA, US
Assignee:
Merck Sharp & Dohme Corp. - Rahway NJ
International Classification:
C07K 16/00 A61K 39/395 C12N 5/07 C12N 5/16
US Classification:
5303871, 4241301, 435326
Abstract:
Antagonists of human proprotein convertase subtilisin-kexin type 9 (“PCSK9”) are disclosed. The disclosed antagonists are effective in the inhibition of PCSK9 function and, accordingly, present desirable antagonists for use in the treatment of conditions associated with PCSK9 activity. The present invention also discloses nucleic acid encoding said antagonists, vectors, host cells, and compositions comprising the antagonists. Methods of making PCSK9-specific antagonists as well as methods of using the antagonists for inhibiting or antagonizing PCSK9 function are also disclosed and form important additional aspects of the present disclosure.
Jon H. Condra - Doylestown PA, US Rose M. Cubbon - Fanwood NJ, US Holly A. Hammond - Telford PA, US Laura Orsatti - Pomezia, IT Shilpa Pandit - Edison NJ, US Laurence B. Peterson - Westfield NJ, US Joseph C. Santoro - Belle Mead NJ, US Ayesha Sitlani - Metuchen NJ, US Dana D. Wood - Collegeville PA, US Henryk Mach - Ambler PA, US Heidi Yoder - Glenside PA, US Sonia M. Gregory - Blue Bell PA, US Jeffrey T. Blue - Telford PA, US Kevin Wang - Lansdale PA, US Peter Luo - Lansdale PA, US Denise K. Nawrocki - Annandale NJ, US Pingyu Zhong - Blue Bell PA, US Feng Dong - Lansdale PA, US Yan Li - San Jose CA, US
Assignee:
Merck Sharp & Dohme Corp. - Rahway NJ
International Classification:
C07K 16/00 A61K 39/395 C12N 5/07 C12N 5/16
US Classification:
5303871, 4241301, 435326
Abstract:
Antagonists of human proprotein convertase subtilisin-kexin type 9 (“PCSK9”) are disclosed. The disclosed antagonists are effective in the inhibition of PCSK9 function and, accordingly, present desirable antagonists for use in the treatment of conditions associated with PCSK9 activity. The present invention also discloses nucleic acid encoding said antagonists, vectors, host cells, and compositions comprising the antagonists. Methods of making PCSK9-specific antagonists as well as methods of using the antagonists for inhibiting or antagonizing PCSK9 function are also disclosed and form important additional aspects of the present disclosure.
Joung Goulet - Wetsfield NJ, US Rose Cubbon - Fanwood NJ, US Richard Cummings - Fanwood NJ, US Xingfang Hong - Westfield NJ, US Peter Sinclair - Scotch Plains NJ, US James Thompson - Fanwood NJ, US
International Classification:
C07D491/14
US Classification:
546/046000
Abstract:
Benzimidazo[4,5-f]isoquinolinone derivatives are inhibitors of Janus protein tyrosine kinases (Jak), and as such are useful as immunosuppressants, and in the treatment of diseases including asthma, allergies, autoimmune diseases.
Yan Ni - Westfield NJ, US Ayesha Sitlani - Metuchen NJ, US Shilpa Pandit - Edison NJ, US Dale Lewis - Washington Crossing PA, US Xun Shen - Piscataway NJ, US Sharon Lobo - Hackettstown NJ, US Timothy McCabe - Doylestown PA, US Jon Condra - Doylestown PA, US Rose Cubbon - Fanwood NJ, US
International Classification:
G01N 33/573
US Classification:
435 74
Abstract:
Methods of using PCSK antagonists More specifically, methods for measuring circulating PCSK levels in a bio-logical sample by means of an immunoassay The immunoassay used can be a solid phase immunoassay, such as a dissociation-enhanced lanthanide fluorescence immunoassay utilizing an E capture antibody or coating and a G or H detecting antibody.
Peter Peizhi Luo - Lansdale PA, US Pingyu Zhong - Blue Bell PA, US Mark Hsieh - Jenkintown PA, US Yan Li - San Jose CA, US Xinwei Wang - Germantown MD, US Feng Dong - Lansdale PA, US Andrei Golosov - Cambridge MA, US Yan Ni - Westfield NJ, US Weirong Wang - Harleysville PA, US Laurence B. Peterson - Westfield NJ, US Rose Cubbon - Fanwood NJ, US Sujata Sharma - Eagleville PA, US Jon Condra - Doylestown PA, US Jun Lu - Lansdale PA, US Gopalakrishnan Parthasarathy - Hillsborough NJ, US Stephen Soisson - Hillsborough NJ, US Noel Byrne - Doylestown PA, US
Antagonists of human proprotein convertase subtilisin-kexin type 9 (“PCSK9”) are disclosed. The disclosed antagonists are effective in the inhibition of PCSK9 function and, accordingly, present desirable antagonists for use in the treatment of conditions associated with PCSK9 activity. The present invention also discloses nucleic acid encoding said antagonists, vectors, host cells, and compositions comprising the antagonists. Methods of making PCSK9-specific antagonists as well as methods of using the antagonists for inhibiting or antagonizing PCSK9 function are also disclosed and form important additional aspects of the present disclosure.
Yan Ni - Westfield NJ, US Ayesha Sitlani - Metuchen NJ, US Shilpa Pandit - Edison NJ, US Dale Lewis - Washington Crossing PA, US Xun Shen - Piscataway NJ, US Sharon Lobo - Hackettstown NJ, US Timothy McCabe - Doylestown PA, US Jon Condra - Doylestown PA, US Rose Cubbon - Fanwood NJ, US Fubao Wang - Drescher PA, US
Antagonists of human proprotein convertase subtilisin-kexin type 9 (PCSK9) are disclosed. Said antagonists are effective in the inhibition of PCSK9 function and thereby provide compositions of matter useful for the treatment of conditions associated with PCSK9 activity. The present invention further discloses nucleic acids encoding PCSK9 antagonists as well as methods of making and using PCSK9 antagonists.
Peter Peizhi Luo - Lansdale PA, US Kevin Caili Wang - Lansdale PA, US Pingyu Zhong - Blue Bell PA, US Mark Hsieh - Jenskintown PA, US Yan Li - San Jose CA, US Xinwei Wang - Germantown MD, US Feng Dong - Lansdale PA, US Andrei Golosov - Cambridge MA, US Yan Ni - Westfield NJ, US Weirong Wang - Harleysville PA, US Laurence B. Peterson - Westfield NJ, US Rose Cubbon - Fanwood NJ, US
Antagonists of human proprotein convertase subtilisin-kexin type 9 (“PCSK9”) are disclosed. The disclosed antagonists are effective in the inhibition of PCSK9 function and, accordingly, present desirable antagonists for use in the treatment of conditions associated with PCSK9 activity. The present invention also discloses nucleic acid encoding said antagonists, vectors, host cells, and compositions comprising the antagonists. Methods of making PCSK9-specific antagonists as well as methods of using the antagonists for inhibiting or antagonizing PCSK9 function are also disclosed and form important additional aspects of the present disclosure.
Jon H. Condra - Doylestown PA, US Rose M. Cubbon - Fanwood NJ, US Holly A. Hammond - Telford PA, US Laura Orsatti - Ponezia, IT Shilpa Pandit - Edison NJ, US Laurence B. Peterson - Westfield NJ, US Joseph C. Santoro - Belle Mead NJ, US Ayesha Sitlani - Metuchen MA, US Dana D. Wood - Collegeville PA, US Henryk Mach - Amber PA, US Heidi Yoder - Glenside PA, US Sonia M. Gregory - Charlottesville VA, US Jeffrey T. Blue - Telford PA, US Kevin Wang - Lansdale PA, US Peizhi (Peter) Luo - Lansdale PA, US Denise K. Nawrocki - Annandale NJ, US Pingyu Zhong - Blue Bell PA, US Feng Dong - Lansdale PA, US Yan Li - San Jose CA, US
Antagonists of human proprotein convertase subtilisin-kexin type 9 (“PCSK9”) are disclosed. The disclosed antagonists are effective in the inhibition of PCSK9 function and, accordingly, present desirable antagonists for use in the treatment of conditions associated with PCSK9 activity. The present invention also discloses nucleic acid encoding said antagonists, vectors, host cells, and compositions comprising the antagonists. Methods of making PCSK9-specific antagonists as well as methods of using the antagonists for inhibiting or antagonizing PCSK9 function are also disclosed and form important additional aspects of the present disclosure.