Abstract: Disclosed are CD70 binding agents, such as humanized anti-CD70 antibodies and fragments and derivatives, that exert a cytotoxic, cytostatic or immunomodulatory on CD70 expressing cells, as well as pharmaceutical compositions and kits comprising the antibody, fragment or derivative. Also disclosed are methods for the treatment of CD70-expressing cancers and immunological disorders, comprising administering to a subject the CD70 binding agents or pharmaceutical compositions.
Abstract: The invention is based in part on the observation that a CHO cell oxidizing enzyme, particularly QSOX1, can survive a seemingly rigorous antibody purification process to reduce subsequent conjugation efficiency of the antibody to a drug. Whether the oxidizing enzyme survives the purification procedure depends on which purification techniques are employed which can vary from one antibody to another. With knowledge that contamination with a CHO cell oxidizing enzyme is a potential problem for subsequent conjugation, a suitable purification scheme can be devised for any antibody that eliminates or at least reduces CHO oxidizing enzyme(s) to an acceptable level.
Type:
Application
Filed:
November 21, 2014
Publication date:
June 8, 2017
Applicant:
SEATTLE GENETICS, INC.
Inventors:
Kevin Beam, Damon Meyer, Bradley Hayes, Robert Lyon, John Valliere-Douglass
Abstract: Disclosed are formulations, including both liquid and lyophilized formulations, comprising a benzodiazepine anti-body-drug conjugate (ADC) and a cyclodextrin. Also disclosed are methods of purifying mixtures comprising benzodiazepine anti-body-drug conjugates and process drug-related impurities.
Type:
Grant
Filed:
March 12, 2014
Date of Patent:
April 4, 2017
Assignee:
Seattle Genetics, Inc.
Inventors:
Hui Li, Shan Jiang, Mary Wallace, Damon Meyer
Abstract: The invention provides murine, chimeric, and humanized antibodies that specifically bind to CD33. The antibodies are useful for treatment and diagnoses of various cancers as well as detecting CD33.
Type:
Grant
Filed:
May 15, 2013
Date of Patent:
March 7, 2017
Assignee:
SEATTLE GENETICS, INC.
Inventors:
May Kung Sutherland, Maureen Ryan, Django Sussman, Patrick Burke, Scott Jeffrey
Abstract: The invention provides methods and compositions for the inhibition of fucosylation of proteins, including antibodies, in vivo by administration of a fucose analog.
Type:
Application
Filed:
October 21, 2016
Publication date:
February 9, 2017
Applicant:
Seattle Genetics, Inc.
Inventors:
Peter Senter, Stephen Alley, Dennis Benjamin
Abstract: A compound, or a pharmaceutically acceptable salt or solvate thereof, or conjugates thereof, selected from the group consisting of formula wherein: (a) R10 is H, and R11 is OH, ORA, where RA is saturated C1-4 alkyl; (b) R10 and R11 form a nitrogen-carbon double bond between the nitrogen and carbon atoms to which they are bound; or (c) R10 is H and R11 is S02M, where z is 2 or 3 and M is a monovalent pharmaceutically acceptable cation, or both M together are a divalent pharmaceutically acceptable cation.
Abstract: Antibody drug conjugates (ADC's) that bind to 158P1D7 protein and variants thereof are described herein. 158P1D7 exhibits tissue specific expression in normal adult tissue, and is aberrantly expressed in glioblastoma, lung cancer, bladder cancer, and breast cancer. Consequently, the ADC's of the invention provide a therapeutic composition for the treatment of cancer.
Type:
Application
Filed:
March 30, 2016
Publication date:
December 22, 2016
Applicants:
AGENSYS, INC., Seattle Genetics, Inc.
Inventors:
Robert Kendall MORRISON, Zili AN, Karen Jane Meyrick MORRISON, Josh SNYDER, Xiao-Chi JIA
Abstract: Auristatin peptide analogs of MeVal-Val-Dil-Dap-Phe (MMAF) having a carboxylic acid equivalent at the C-terminal phenylalanine were prepared and attached to ligands through various linkers, including maleimidocaproyl-val-cit-PAB. The resulting ligand-drug conjugates were active in vitro and in vivo in inhibiting cell proliferation and are represented by the general structure of Lv-[(LU)0-1-(D)1-4]p wherein L- is Ligand unit; LU is a Linker unit (LU); v is 1; p is an number ranging from about 1 to about 20; and D is a drug moiety having the formula: wherein the moiety —N(R9)Z1 is a phenylalanine bioisostere, wherein Z1 is —CH(R10)Z2 so that the phenylalanine bioisostere has the structure of Formula A: and wherein the substituents R2-R10, X1 and Z2 are as defined.
Type:
Grant
Filed:
September 30, 2014
Date of Patent:
December 20, 2016
Assignee:
Seattle Genetics, Inc.
Inventors:
Svetlana O Doronina, Toni Beth Kline, Scott Jeffrey, Peter D Senter, Damon Meyer
Abstract: The invention provides methods and compositions for the inhibition of fucosylation of proteins, including antibodies, in vivo by administration of a fucose analog.
Type:
Grant
Filed:
August 5, 2011
Date of Patent:
November 29, 2016
Assignee:
Seattle Genetics, Inc.
Inventors:
Peter Senter, Stephen Alley, Dennis Benjamin
Abstract: The invention provides antibodies that specifically bind to integrin ?v?6. The antibodies are useful for treatment and diagnoses of various cancers as well as detecting ?v?6.
Abstract: The present invention provides Ligand-Drug Conjugates comprising a PEG Unit in a parallel orientation to the Drug Unit. The invention provides inter alia, Ligand-Drug Conjugates (LDCs), methods of preparing and using them, and intermediates thereof. The Ligand-Drug Conjugates are stable in circulation, yet capable of inflicting cell death on targeted cells or inhibiting proliferation of targeted cells once its drug cargo is released in the vicinity or within targeted cells. In principle embodiments, an LDC of the present invention is represented by the structure of Formula I.
Type:
Application
Filed:
October 14, 2014
Publication date:
October 27, 2016
Applicant:
SEATTLE GENETICS, INC.
Inventors:
Robert Lyon, Patrick Burke, Joshua Hunter
Abstract: Drug Linker compounds and Drug Linker Ligand conjugates are provided that have auristatins linked via the C-terminus. The conjugates show efficacy without the need for a self-immolative group to release the drug.
Type:
Grant
Filed:
October 23, 2013
Date of Patent:
October 11, 2016
Assignee:
Seattle Genetics, Inc.
Inventors:
Peter Senter, Svetlana Doronina, Timothy Bovee