WO2026080697A1 - Conjugués d'anticorps à rapports élevés charge utile/anticorps, compositions les comprenant, et leurs procédés d'utilisation - Google Patents

Conjugués d'anticorps à rapports élevés charge utile/anticorps, compositions les comprenant, et leurs procédés d'utilisation

Info

Publication number
WO2026080697A1
WO2026080697A1 PCT/US2025/050221 US2025050221W WO2026080697A1 WO 2026080697 A1 WO2026080697 A1 WO 2026080697A1 US 2025050221 W US2025050221 W US 2025050221W WO 2026080697 A1 WO2026080697 A1 WO 2026080697A1
Authority
WO
WIPO (PCT)
Prior art keywords
antibody
formula
alkylene
independently
antibody conjugate
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
PCT/US2025/050221
Other languages
English (en)
Inventor
Garrett Geoffrey GROSS
Daniel Calarese
Gang Yin
Krishna Mohan BAJJURI
Amandeep Kaur GAKHAL
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sutro Biopharma Inc
Original Assignee
Sutro Biopharma Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sutro Biopharma Inc filed Critical Sutro Biopharma Inc
Publication of WO2026080697A1 publication Critical patent/WO2026080697A1/fr
Pending legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/68Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
    • A61K47/6801Drug-antibody or immunoglobulin conjugates defined by the pharmacologically or therapeutically active agent
    • A61K47/6803Drugs conjugated to an antibody or immunoglobulin, e.g. cisplatin-antibody conjugates
    • A61K47/68037Drugs conjugated to an antibody or immunoglobulin, e.g. cisplatin-antibody conjugates the drug being a camptothecin [CPT] or derivatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/68Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
    • A61K47/6835Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site
    • A61K47/6851Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site the antibody targeting a determinant of a tumour cell
    • A61K47/6855Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site the antibody targeting a determinant of a tumour cell the tumour determinant being from breast cancer cell
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/68Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
    • A61K47/6889Conjugates wherein the antibody being the modifying agent and wherein the linker, binder or spacer confers particular properties to the conjugates, e.g. peptidic enzyme-labile linkers or acid-labile linkers, providing for an acid-labile immuno conjugate wherein the drug may be released from its antibody conjugated part in an acidic, e.g. tumoural or environment

Landscapes

  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Immunology (AREA)
  • Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Cell Biology (AREA)
  • Oncology (AREA)
  • Peptides Or Proteins (AREA)

Abstract

La présente divulgation concerne des conjugués d'anticorps, notamment des conjugués anticorps-médicament, comprenant de multiples charges utiles à des rapports élevés charge utile/anticorps, des compositions pharmaceutiques associées, ainsi que l'utilisation des conjugués d'anticorps et de leurs compositions pour le traitement de maladies et de troubles, notamment de maladies prolifératives.
PCT/US2025/050221 2024-10-09 2025-10-09 Conjugués d'anticorps à rapports élevés charge utile/anticorps, compositions les comprenant, et leurs procédés d'utilisation Pending WO2026080697A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US202463705389P 2024-10-09 2024-10-09
US63/705,389 2024-10-09

Publications (1)

Publication Number Publication Date
WO2026080697A1 true WO2026080697A1 (fr) 2026-04-16

Family

ID=97752521

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2025/050221 Pending WO2026080697A1 (fr) 2024-10-09 2025-10-09 Conjugués d'anticorps à rapports élevés charge utile/anticorps, compositions les comprenant, et leurs procédés d'utilisation

Country Status (1)

Country Link
WO (1) WO2026080697A1 (fr)

Citations (142)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4289872A (en) 1979-04-06 1981-09-15 Allied Corporation Macromolecular highly branched homogeneous compound based on lysine units
US4486414A (en) 1983-03-21 1984-12-04 Arizona Board Of Reagents Dolastatins A and B cell growth inhibitory substances
US4542225A (en) 1984-08-29 1985-09-17 Dana-Farber Cancer Institute, Inc. Acid-cleavable compound
US4560655A (en) 1982-12-16 1985-12-24 Immunex Corporation Serum-free cell culture medium and process for making same
US4625014A (en) 1984-07-10 1986-11-25 Dana-Farber Cancer Institute, Inc. Cell-delivery agent
WO1987000195A1 (fr) 1985-06-28 1987-01-15 Celltech Limited Culture de cellules animales
US4657866A (en) 1982-12-21 1987-04-14 Sudhir Kumar Serum-free, synthetic, completely chemically defined tissue culture media
US4671958A (en) 1982-03-09 1987-06-09 Cytogen Corporation Antibody conjugates for the delivery of compounds to target sites
US4753894A (en) 1984-02-08 1988-06-28 Cetus Corporation Monoclonal anti-human breast cancer antibodies
US4767704A (en) 1983-10-07 1988-08-30 Columbia University In The City Of New York Protein-free culture medium
US4816444A (en) 1987-07-10 1989-03-28 Arizona Board Of Regents, Arizona State University Cell growth inhibitory substance
US4816567A (en) 1983-04-08 1989-03-28 Genentech, Inc. Recombinant immunoglobin preparations
US4879278A (en) 1989-05-16 1989-11-07 Arizona Board Of Regents Isolation and structural elucidation of the cytostatic linear depsipeptide dolastatin 15
WO1990003430A1 (fr) 1988-09-23 1990-04-05 Cetus Corporation Milieu de culture de cellules pour l'amelioration de la croissance des cellules, de la longivite de la culture et de l'expression du produit
US4927762A (en) 1986-04-01 1990-05-22 Cell Enterprises, Inc. Cell culture medium with antioxidant
WO1990005719A1 (fr) 1988-11-23 1990-05-31 British Bio-Technology Limited Inhibiteurs de collagenase a base d'acide hydroxamique
US4943533A (en) 1984-03-01 1990-07-24 The Regents Of The University Of California Hybrid cell lines that produce monoclonal antibodies to epidermal growth factor receptor
US4978744A (en) 1989-01-27 1990-12-18 Arizona Board Of Regents Synthesis of dolastatin 10
US4986988A (en) 1989-05-18 1991-01-22 Arizona Board Of Regents Isolation and structural elucidation of the cytostatic linear depsipeptides dolastatin 13 and dehydrodolastatin 13
US5076973A (en) 1988-10-24 1991-12-31 Arizona Board Of Regents Synthesis of dolastatin 3
US5122469A (en) 1990-10-03 1992-06-16 Genentech, Inc. Method for culturing Chinese hamster ovary cells to improve production of recombinant proteins
US5138036A (en) 1989-11-13 1992-08-11 Arizona Board Of Regents Acting On Behalf Of Arizona State University Isolation and structural elucidation of the cytostatic cyclodepsipeptide dolastatin 14
US5204244A (en) 1987-10-27 1993-04-20 Oncogen Production of chimeric antibodies by homologous recombination
US5229275A (en) 1990-04-26 1993-07-20 Akzo N.V. In-vitro method for producing antigen-specific human monoclonal antibodies
US5229490A (en) 1987-05-06 1993-07-20 The Rockefeller University Multiple antigen peptide system
WO1993021259A1 (fr) 1992-04-14 1993-10-28 Cornell Research Foundation Inc. Macromolecules dendritiques et leur procede de production
EP0606046A1 (fr) 1993-01-06 1994-07-13 Ciba-Geigy Ag Arylsulfonamido-substitués dérivés d'acides hydroxamic
US5410024A (en) 1993-01-21 1995-04-25 Arizona Board Of Regents Acting On Behalf Of Arizona State University Human cancer inhibitory pentapeptide amides
WO1995020045A1 (fr) 1994-01-21 1995-07-27 The Institute Of Cancer Research: Royal Cancer Hospital Anticorps contre le recepteur d'egf et leur effet antitumeur
US5500362A (en) 1987-01-08 1996-03-19 Xoma Corporation Chimeric antibody with specificity to human B cell surface antigen
US5504191A (en) 1994-08-01 1996-04-02 Arizona Board Of Regents Acting On Behalf Of Arizona State University Human cancer inhibitory pentapeptide methyl esters
US5521284A (en) 1994-08-01 1996-05-28 Arizona Board Of Regents Acting On Behalf Of Arizona State University Human cancer inhibitory pentapeptide amides and esters
US5530097A (en) 1994-08-01 1996-06-25 Arizona Board Of Regents Acting On Behalf Of Arizona State University Human cancer inhibitory peptide amides
US5534615A (en) 1994-04-25 1996-07-09 Genentech, Inc. Cardiac hypertrophy factor and uses therefor
WO1996021469A1 (fr) 1995-01-10 1996-07-18 Shearwater Polymers, Inc. Derives multibras monofonctionnels et stables du point de vue hydrolitique de poly(ethylene glycol), et polymeres apparentes pourla modification de surfaces et de molecules
US5545807A (en) 1988-10-12 1996-08-13 The Babraham Institute Production of antibodies from transgenic animals
US5554725A (en) 1994-09-14 1996-09-10 Arizona Board Of Regents Acting On Behalf Of Arizona State University Synthesis of dolastatin 15
WO1996027583A1 (fr) 1995-03-08 1996-09-12 Pfizer Inc. Derives de l'acide arylsulfonylamino hydroxamique
US5558864A (en) 1991-03-06 1996-09-24 Merck Patent Gesellschaft Mit Beschrankter Haftung Humanized and chimeric anti-epidermal growth factor receptor monoclonal antibodies
US5565332A (en) 1991-09-23 1996-10-15 Medical Research Council Production of chimeric antibodies - a combinatorial approach
US5567610A (en) 1986-09-04 1996-10-22 Bioinvent International Ab Method of producing human monoclonal antibodies and kit therefor
WO1996033172A1 (fr) 1995-04-20 1996-10-24 Pfizer Inc. Derives d'acide hydroxamique arylsufonyle en tant qu'inhibiteurs de mmp et de tnf
US5573905A (en) 1992-03-30 1996-11-12 The Scripps Research Institute Encoded combinatorial chemical libraries
US5585089A (en) 1988-12-28 1996-12-17 Protein Design Labs, Inc. Humanized immunoglobulins
WO1996040210A1 (fr) 1995-06-07 1996-12-19 Imclone Systems Incorporated Anticorps et fragments d'anticorps inhibant la croissance des tumeurs
US5589369A (en) 1992-02-11 1996-12-31 Cell Genesys Inc. Cells homozygous for disrupted target loci
US5591669A (en) 1988-12-05 1997-01-07 Genpharm International, Inc. Transgenic mice depleted in a mature lymphocytic cell-type
US5599902A (en) 1994-11-10 1997-02-04 Arizona Board Of Regents Acting On Behalf Of Arizona State University Cancer inhibitory peptides
US5635483A (en) 1992-12-03 1997-06-03 Arizona Board Of Regents Acting On Behalf Of Arizona State University Tumor inhibiting tetrapeptide bearing modified phenethyl amides
EP0780386A1 (fr) 1995-12-20 1997-06-25 F. Hoffmann-La Roche Ag Inhibiteurs de métalloprotéases matricielles
WO1997022596A1 (fr) 1995-12-18 1997-06-26 Zeneca Limited Derives de quinazoline
US5643575A (en) 1993-10-27 1997-07-01 Enzon, Inc. Non-antigenic branched polymer conjugates
WO1997030035A1 (fr) 1996-02-13 1997-08-21 Zeneca Limited Derives de la quinazoline utilises comme inhibiteurs du vegf
US5663149A (en) 1994-12-13 1997-09-02 Arizona Board Of Regents Acting On Behalf Of Arizona State University Human cancer inhibitory pentapeptide heterocyclic and halophenyl amides
WO1997032856A1 (fr) 1996-03-05 1997-09-12 Zeneca Limited Derives de 4-anilinoquinazoline
US5677171A (en) 1988-01-12 1997-10-14 Genentech, Inc. Monoclonal antibodies directed to the HER2 receptor
EP0818442A2 (fr) 1996-07-12 1998-01-14 Pfizer Inc. Dérivés cycliques de sulfones comme inhibiteurs de métalloprotéinase et de la production du facteur de nécrose des tumeurs
WO1998003516A1 (fr) 1996-07-18 1998-01-29 Pfizer Inc. Composes a base de phosphinate inhibiteurs des metalloproteases matricielles
WO1998007697A1 (fr) 1996-08-23 1998-02-26 Pfizer Inc. Derives de l'acide arylsulfonylamino hydroxamique
WO1998013354A1 (fr) 1996-09-25 1998-04-02 Zeneca Limited Derives quinazolines et compositions pharmaceutiques les contenant
US5736137A (en) 1992-11-13 1998-04-07 Idec Pharmaceuticals Corporation Therapeutic application of chimeric and radiolabeled antibodies to human B lymphocyte restricted differentiation antigen for treatment of B cell lymphoma
US5780588A (en) 1993-01-26 1998-07-14 Arizona Board Of Regents Elucidation and synthesis of selected pentapeptides
WO1998030566A1 (fr) 1997-01-06 1998-07-16 Pfizer Inc. Derives de sulfone cyclique
US5789554A (en) 1994-08-12 1998-08-04 Immunomedics, Inc. Immunoconjugates and humanized antibodies specific for B-cell lymphoma and leukemia cells
WO1998033768A1 (fr) 1997-02-03 1998-08-06 Pfizer Products Inc. Derives d'acide arylsulfonylaminohydroxamique
WO1998034918A1 (fr) 1997-02-11 1998-08-13 Pfizer Inc. Derives de l'acide arylsulfonylhydroxamique
WO1998034915A1 (fr) 1997-02-07 1998-08-13 Pfizer Inc. Derives du n-hxdroxy-beta-sulfonyl-propionamide et leur utilisation comme inhibiteurs des metalloproteases matrices
WO1998035985A1 (fr) 1997-02-12 1998-08-20 The Regents Of The University Of Michigan Proteines-marqueurs pour le cancer du poumon et utilisation de ces dernieres
WO1999007675A1 (fr) 1997-08-08 1999-02-18 Pfizer Products Inc. Derives de l'acide aryloxyarylsulfonylamino hydroxamique
US5891996A (en) 1972-09-17 1999-04-06 Centro De Inmunologia Molecular Humanized and chimeric monoclonal antibodies that recognize epidermal growth factor receptor (EGF-R); diagnostic and therapeutic use
WO1999029667A1 (fr) 1997-12-05 1999-06-17 Pfizer Limited Derives d'acide hydroxamique utilises comme inhibiteurs de metalloproteases matricielles
EP0931788A2 (fr) 1998-01-27 1999-07-28 Pfizer Limited Inhibiteurs de la métalloprotéinase
EP0945864A2 (fr) 1998-03-26 1999-09-29 Sony Corporation Sélection de matériau vidéo
WO1999052889A1 (fr) 1998-04-10 1999-10-21 Pfizer Products Inc. Hydroxamides de l'acide (4-arylsulfonylamino)-tetrahydropyrane-4-carboxylique
WO1999052910A1 (fr) 1998-04-10 1999-10-21 Pfizer Products Inc. Derives bicycliques de l'acide hydroxamique
US6034065A (en) 1992-12-03 2000-03-07 Arizona Board Of Regents Elucidation and synthesis of antineoplastic tetrapeptide phenethylamides of dolastatin 10
EP1004578A2 (fr) 1998-11-05 2000-05-31 Pfizer Products Inc. Dérivés d'hydroxamide de l'acide 5-oxo-pyrrolidine-2-carboxylique
WO2000034337A1 (fr) 1998-12-10 2000-06-15 Tsukuba Research Laboratory, Toagosei Co., Ltd. Anticorps monoclonaux humanises luttant contre un facteur de croissance de cellules endotheliales vasculaires
WO2000047212A1 (fr) 1999-02-10 2000-08-17 Astrazeneca Ab Derives de quinazoline utilises comme inhibiteurs de l'angiogenese
US6130237A (en) 1996-09-12 2000-10-10 Cancer Research Campaign Technology Limited Condensed N-aclyindoles as antitumor agents
WO2001032651A1 (fr) 1999-11-05 2001-05-10 Astrazeneca Ab Derives de quinazoline utilises en tant qu'inhibiteurs du facteur de croissance endotheliale vasculaire (vegf)
US6235883B1 (en) 1997-05-05 2001-05-22 Abgenix, Inc. Human monoclonal antibodies to epidermal growth factor receptor
US6239104B1 (en) 1997-02-25 2001-05-29 Arizona Board Of Regents Isolation and structural elucidation of the cytostatic linear and cyclo-depsipeptides dolastatin 16, dolastatin 17, and dolastatin 18
US6258562B1 (en) 1996-02-09 2001-07-10 Basf Aktiengesellschaft Human antibodies that bind human TNFα
WO2001060814A2 (fr) 2000-02-15 2001-08-23 Sugen, Inc. Inhibiteurs de la proteine kinase 2-indolinone a substitution pyrrole
US6281211B1 (en) 1999-02-04 2001-08-28 Euro-Celtique S.A. Substituted semicarbazides and the use thereof
WO2001062931A2 (fr) 2000-02-25 2001-08-30 The Government Of The United States, As Represented By The Secretary Of The Department Of Health And Human Services SCFV ANTI-EGFRvIII POSSEDANT UNE CYTOTOXICITE ET UN RENDEMENT AMELIORES, IMMUNOTOXINES A BASE DE CES SCFV ET PROCEDE D'UTILISATION ASSOCIE
WO2001088138A1 (fr) 2000-05-19 2001-11-22 Scancell Limited Anticorps humanises contre le recepteur du facteur de croissance epidermique
US6323315B1 (en) 1999-09-10 2001-11-27 Basf Aktiengesellschaft Dolastatin peptides
US6423685B1 (en) 1998-03-05 2002-07-23 Chiron Corporation Method for increasing the serum half-life of a biologically active molecule
WO2002085923A2 (fr) 2001-04-19 2002-10-31 The Scripps Research Institute Incorporation in vivo d'acides amines non naturels
WO2002088172A2 (fr) 2001-04-30 2002-11-07 Seattle Genetics, Inc. Composes pentapeptidiques et leurs utilisations
US20030083263A1 (en) 2001-04-30 2003-05-01 Svetlana Doronina Pentapeptide compounds and uses related thereto
WO2003039486A2 (fr) 2001-11-09 2003-05-15 Idec Pharmaceuticals Corporation Anticorps anti-cd80 presentant une activite adcc visant la mort des cellules b de lymphome a mediation par adcc, isolement ou en combinaison avec d'autres therapies
US20030143596A1 (en) 2001-11-07 2003-07-31 Shearwater Corporation Branched polymers and their conjugates
WO2004010957A2 (fr) 2002-07-31 2004-02-05 Seattle Genetics, Inc. Conjugues de medicaments et leur utilisation dans le traitement du cancer, d'une maladie auto-immune ou d'une maladie infectieuse
EP1444268A2 (fr) 2001-11-12 2004-08-11 Gundram Jung Molecule d'anticorps anti-cd28 bispecifique
US6914128B1 (en) 1999-03-25 2005-07-05 Abbott Gmbh & Co. Kg Human antibodies that bind human IL-12 and methods for producing
US20050147610A1 (en) 2003-11-12 2005-07-07 Tariq Ghayur IL-18 binding proteins
US20050238649A1 (en) 2003-11-06 2005-10-27 Seattle Genetics, Inc. Monomethylvaline compounds capable of conjugation to ligands
WO2005111082A1 (fr) 2004-04-30 2005-11-24 Inserm (Institut National De La Sante Et De La Recherche Medicale) Anticorps anti-tfr
WO2006026306A1 (fr) 2004-08-31 2006-03-09 Biogen Idec Ma Inc. Pyrimidinylimidazoles utilises comme inhibiteurs de tgf-beta
WO2007076086A2 (fr) 2005-12-22 2007-07-05 Biogen Idec Ma Inc Modulateurs du facteur de croissance transformant
WO2007076127A2 (fr) 2005-12-22 2007-07-05 Biogen Idec Ma Inc Modulateurs du facteur de croissance transformant
US7247301B2 (en) 2001-06-13 2007-07-24 Genmab A/S Human monoclonal antibodies to epidermal growth factor receptor (EGFR)
WO2007124299A2 (fr) 2006-04-21 2007-11-01 Novartis Ag Compositions pharmaceutiques d'anticorps anti-cd40 antagoniste
US7375078B2 (en) 2004-02-23 2008-05-20 Genentech, Inc. Heterocyclic self-immolative linkers and conjugates
WO2009009059A1 (fr) 2007-07-09 2009-01-15 Biogen Idec Ma Inc. Composés spiro en tant qu'antagonistes du tgf-bêta
US20100137386A1 (en) 2008-12-01 2010-06-03 Tesshi Yamada Tnik inhibitor and the use
US20100216795A1 (en) 2008-12-01 2010-08-26 Tesshi Yamada Tnik inhibitor and the use
US8080568B1 (en) 2010-06-29 2011-12-20 Ewha University - Industry Collaboration Foundation 2-pyridyl substituted imidazoles as therapeutic ALK5 and/or ALK4 inhibitors
US8258082B2 (en) 2000-12-18 2012-09-04 Dyax Corp. Focused libraries of genetic packages
US20120225061A1 (en) 2011-03-04 2012-09-06 Matthew Burger Tetrasubstituted cyclohexyl compounds as kinase inhibitors
US8431558B2 (en) 2004-11-01 2013-04-30 The Regents Of The University Of California Compositions and methods for modification of biomolecules
US20130189287A1 (en) 2011-12-23 2013-07-25 Paul Scherrer Institut Enzymatic conjugation of polypeptides
US20130251783A1 (en) 2011-09-14 2013-09-26 Universitat Heidelberg Liposomes containing permeation enhancers for oral drug delivery
WO2013185115A1 (fr) 2012-06-08 2013-12-12 Sutro Biopharma, Inc. Anticorps comprenant des résidus d'acides aminés non endogènes spécifiques d'un site, leurs procédés de préparation et leurs procédés d'utilisation
WO2014036022A1 (fr) 2012-08-29 2014-03-06 Amgen Inc. Composés quinazolinones et leurs dérivés
US8691730B2 (en) 2007-09-14 2014-04-08 Adimab, Llc Rationally designed, synthetic antibody libraries and uses therefor
US8703936B2 (en) 2010-02-12 2014-04-22 The Regents Of The University Of California Compositions and methods for modification of biomolecules
US20140249135A1 (en) 2007-03-01 2014-09-04 Novartis Ag Pim kinase inhibitors and methods of their use
WO2015006555A2 (fr) 2013-07-10 2015-01-15 Sutro Biopharma, Inc. Anticorps comprenant plusieurs résidus d'acides aminés non naturels site-spécifiques, des procédés permettant leur préparation et leurs méthodes d'utilisation
US20150045368A1 (en) 2012-03-05 2015-02-12 Amgen Inc. Oxazolidinone compounds and derivatives thereof
WO2015083833A1 (fr) 2013-12-06 2015-06-11 カルナバイオサイエンス株式会社 Nouveau dérivé quinazoline
WO2015136073A1 (fr) 2014-03-14 2015-09-17 Oncodesign Sa Inhibiteurs macrocycliques de la kinase tgf-br2
US9145361B2 (en) 2011-03-25 2015-09-29 Life Technologies Corporation SDP-containing heterobifunctional agents
US9222940B2 (en) 2010-04-27 2015-12-29 Synaffix B.V. Fused cyclooctyne compounds and their use in metal-free click reactions
WO2016020864A1 (fr) 2014-08-06 2016-02-11 Novartis Ag Inhibiteurs de protéine kinase c et leurs procédés d'utilisation
WO2016123582A1 (fr) 2015-01-30 2016-08-04 Sutro Biopharma, Inc. Dérivés d'hémiasterline pour conjugaison et thérapie
WO2017076484A1 (fr) 2015-11-02 2017-05-11 Merck Patent Gmbh Dérivés de 1,4-dicarbonyle-pipéridyle
CN107226808A (zh) 2016-03-23 2017-10-03 山东轩竹医药科技有限公司 端锚聚合酶抑制剂
WO2018003962A1 (fr) 2016-06-30 2018-01-04 国立研究開発法人理化学研究所 Nouveau composé ou son sel pharmaceutiquement accepté
WO2018046933A1 (fr) 2016-09-08 2018-03-15 University Of Bath Inhibiteurs de tankyrase
EP3313177A1 (fr) 2015-06-26 2018-05-02 Zobele Holding SpA Dispositif permettant de piéger des insectes
US20180127426A1 (en) 2015-03-02 2018-05-10 Rigel Pharmaceuticals, Inc. TGF-Beta Inhibitors
US10596270B2 (en) 2017-09-18 2020-03-24 Sutro Biopharma, Inc. Anti-folate receptor antibody conjugates, compositions comprising anti-folate receptor antibody conjugates, and methods of making and using anti-folate receptor antibody conjugates
WO2020252015A1 (fr) 2019-06-10 2020-12-17 Sutro Biopharma, Inc. Conjugués anticorps-médicament immunomodulateurs et utilisations associées
WO2023207710A1 (fr) * 2022-04-29 2023-11-02 四川科伦博泰生物医药股份有限公司 Conjugué anticorps-médicament, composition pharmaceutique de celui-ci et son utilisation
WO2024006272A1 (fr) 2022-06-27 2024-01-04 Sutro Biopharma, Inc. CHARGES UTILES DE LIEUR β-GLUCURONIDE, LEURS CONJUGUÉS PROTÉIQUES ET MÉTHODES ASSOCIÉES
WO2024006542A1 (fr) * 2022-06-30 2024-01-04 Sutro Biopharma, Inc. Anticorps anti-ror1 et conjugués d'anticorps, compositions comprenant des anticorps anti-ror1 ou des conjugués d'anticorps, et méthodes de fabrication et d'utilisation d'anticorps anti-ror1 et de conjugués d'anticorps
EP4410313A1 (fr) * 2023-01-31 2024-08-07 Synaffix B.V. Conjugués d'anticorps homogènes à charge utile élevée
US20240261426A1 (en) * 2021-06-28 2024-08-08 Byondis B.V. Conjugates comprising phosphoantigens and their use in therapy

Patent Citations (159)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5891996A (en) 1972-09-17 1999-04-06 Centro De Inmunologia Molecular Humanized and chimeric monoclonal antibodies that recognize epidermal growth factor receptor (EGF-R); diagnostic and therapeutic use
US4289872A (en) 1979-04-06 1981-09-15 Allied Corporation Macromolecular highly branched homogeneous compound based on lysine units
US4671958A (en) 1982-03-09 1987-06-09 Cytogen Corporation Antibody conjugates for the delivery of compounds to target sites
US4560655A (en) 1982-12-16 1985-12-24 Immunex Corporation Serum-free cell culture medium and process for making same
US4657866A (en) 1982-12-21 1987-04-14 Sudhir Kumar Serum-free, synthetic, completely chemically defined tissue culture media
US4486414A (en) 1983-03-21 1984-12-04 Arizona Board Of Reagents Dolastatins A and B cell growth inhibitory substances
US4816567A (en) 1983-04-08 1989-03-28 Genentech, Inc. Recombinant immunoglobin preparations
US4767704A (en) 1983-10-07 1988-08-30 Columbia University In The City Of New York Protein-free culture medium
US4753894A (en) 1984-02-08 1988-06-28 Cetus Corporation Monoclonal anti-human breast cancer antibodies
US4943533A (en) 1984-03-01 1990-07-24 The Regents Of The University Of California Hybrid cell lines that produce monoclonal antibodies to epidermal growth factor receptor
US4625014A (en) 1984-07-10 1986-11-25 Dana-Farber Cancer Institute, Inc. Cell-delivery agent
US4542225A (en) 1984-08-29 1985-09-17 Dana-Farber Cancer Institute, Inc. Acid-cleavable compound
US4618492A (en) 1984-08-29 1986-10-21 Dana-Farber Cancer Institute, Inc. Acid-cleavable compound
WO1987000195A1 (fr) 1985-06-28 1987-01-15 Celltech Limited Culture de cellules animales
US4927762A (en) 1986-04-01 1990-05-22 Cell Enterprises, Inc. Cell culture medium with antioxidant
US5567610A (en) 1986-09-04 1996-10-22 Bioinvent International Ab Method of producing human monoclonal antibodies and kit therefor
US5500362A (en) 1987-01-08 1996-03-19 Xoma Corporation Chimeric antibody with specificity to human B cell surface antigen
US5229490A (en) 1987-05-06 1993-07-20 The Rockefeller University Multiple antigen peptide system
US4816444A (en) 1987-07-10 1989-03-28 Arizona Board Of Regents, Arizona State University Cell growth inhibitory substance
US5204244A (en) 1987-10-27 1993-04-20 Oncogen Production of chimeric antibodies by homologous recombination
US5677171A (en) 1988-01-12 1997-10-14 Genentech, Inc. Monoclonal antibodies directed to the HER2 receptor
WO1990003430A1 (fr) 1988-09-23 1990-04-05 Cetus Corporation Milieu de culture de cellules pour l'amelioration de la croissance des cellules, de la longivite de la culture et de l'expression du produit
US5545807A (en) 1988-10-12 1996-08-13 The Babraham Institute Production of antibodies from transgenic animals
US5076973A (en) 1988-10-24 1991-12-31 Arizona Board Of Regents Synthesis of dolastatin 3
WO1990005719A1 (fr) 1988-11-23 1990-05-31 British Bio-Technology Limited Inhibiteurs de collagenase a base d'acide hydroxamique
US5591669A (en) 1988-12-05 1997-01-07 Genpharm International, Inc. Transgenic mice depleted in a mature lymphocytic cell-type
US5585089A (en) 1988-12-28 1996-12-17 Protein Design Labs, Inc. Humanized immunoglobulins
US6180370B1 (en) 1988-12-28 2001-01-30 Protein Design Labs, Inc. Humanized immunoglobulins and methods of making the same
US5693762A (en) 1988-12-28 1997-12-02 Protein Design Labs, Inc. Humanized immunoglobulins
US5693761A (en) 1988-12-28 1997-12-02 Protein Design Labs, Inc. Polynucleotides encoding improved humanized immunoglobulins
US4978744A (en) 1989-01-27 1990-12-18 Arizona Board Of Regents Synthesis of dolastatin 10
US4879278A (en) 1989-05-16 1989-11-07 Arizona Board Of Regents Isolation and structural elucidation of the cytostatic linear depsipeptide dolastatin 15
US4986988A (en) 1989-05-18 1991-01-22 Arizona Board Of Regents Isolation and structural elucidation of the cytostatic linear depsipeptides dolastatin 13 and dehydrodolastatin 13
US5138036A (en) 1989-11-13 1992-08-11 Arizona Board Of Regents Acting On Behalf Of Arizona State University Isolation and structural elucidation of the cytostatic cyclodepsipeptide dolastatin 14
US5229275A (en) 1990-04-26 1993-07-20 Akzo N.V. In-vitro method for producing antigen-specific human monoclonal antibodies
US5122469A (en) 1990-10-03 1992-06-16 Genentech, Inc. Method for culturing Chinese hamster ovary cells to improve production of recombinant proteins
US5558864A (en) 1991-03-06 1996-09-24 Merck Patent Gesellschaft Mit Beschrankter Haftung Humanized and chimeric anti-epidermal growth factor receptor monoclonal antibodies
US5565332A (en) 1991-09-23 1996-10-15 Medical Research Council Production of chimeric antibodies - a combinatorial approach
US5589369A (en) 1992-02-11 1996-12-31 Cell Genesys Inc. Cells homozygous for disrupted target loci
US5573905A (en) 1992-03-30 1996-11-12 The Scripps Research Institute Encoded combinatorial chemical libraries
WO1993021259A1 (fr) 1992-04-14 1993-10-28 Cornell Research Foundation Inc. Macromolecules dendritiques et leur procede de production
US5736137A (en) 1992-11-13 1998-04-07 Idec Pharmaceuticals Corporation Therapeutic application of chimeric and radiolabeled antibodies to human B lymphocyte restricted differentiation antigen for treatment of B cell lymphoma
US5635483A (en) 1992-12-03 1997-06-03 Arizona Board Of Regents Acting On Behalf Of Arizona State University Tumor inhibiting tetrapeptide bearing modified phenethyl amides
US6034065A (en) 1992-12-03 2000-03-07 Arizona Board Of Regents Elucidation and synthesis of antineoplastic tetrapeptide phenethylamides of dolastatin 10
EP0606046A1 (fr) 1993-01-06 1994-07-13 Ciba-Geigy Ag Arylsulfonamido-substitués dérivés d'acides hydroxamic
US5410024A (en) 1993-01-21 1995-04-25 Arizona Board Of Regents Acting On Behalf Of Arizona State University Human cancer inhibitory pentapeptide amides
US5780588A (en) 1993-01-26 1998-07-14 Arizona Board Of Regents Elucidation and synthesis of selected pentapeptides
US5643575A (en) 1993-10-27 1997-07-01 Enzon, Inc. Non-antigenic branched polymer conjugates
WO1995020045A1 (fr) 1994-01-21 1995-07-27 The Institute Of Cancer Research: Royal Cancer Hospital Anticorps contre le recepteur d'egf et leur effet antitumeur
US5534615A (en) 1994-04-25 1996-07-09 Genentech, Inc. Cardiac hypertrophy factor and uses therefor
US5504191A (en) 1994-08-01 1996-04-02 Arizona Board Of Regents Acting On Behalf Of Arizona State University Human cancer inhibitory pentapeptide methyl esters
US5530097A (en) 1994-08-01 1996-06-25 Arizona Board Of Regents Acting On Behalf Of Arizona State University Human cancer inhibitory peptide amides
US5665860A (en) 1994-08-01 1997-09-09 Arizona Board Of Regents Acting On Behalf Of Arizona State University Human cancer inhibitory peptide amides
US5521284A (en) 1994-08-01 1996-05-28 Arizona Board Of Regents Acting On Behalf Of Arizona State University Human cancer inhibitory pentapeptide amides and esters
US5789554A (en) 1994-08-12 1998-08-04 Immunomedics, Inc. Immunoconjugates and humanized antibodies specific for B-cell lymphoma and leukemia cells
US5554725A (en) 1994-09-14 1996-09-10 Arizona Board Of Regents Acting On Behalf Of Arizona State University Synthesis of dolastatin 15
US5599902A (en) 1994-11-10 1997-02-04 Arizona Board Of Regents Acting On Behalf Of Arizona State University Cancer inhibitory peptides
US6506883B2 (en) 1994-11-18 2003-01-14 Centro De Inmunologia Molecular Humanized and chimeric monoclonal antibodies that recognize epidermal growth factor receptor (EGF-R); diagnostic and therapeutic use
US5663149A (en) 1994-12-13 1997-09-02 Arizona Board Of Regents Acting On Behalf Of Arizona State University Human cancer inhibitory pentapeptide heterocyclic and halophenyl amides
US5932462A (en) 1995-01-10 1999-08-03 Shearwater Polymers, Inc. Multiarmed, monofunctional, polymer for coupling to molecules and surfaces
WO1996021469A1 (fr) 1995-01-10 1996-07-18 Shearwater Polymers, Inc. Derives multibras monofonctionnels et stables du point de vue hydrolitique de poly(ethylene glycol), et polymeres apparentes pourla modification de surfaces et de molecules
US5863949A (en) 1995-03-08 1999-01-26 Pfizer Inc Arylsulfonylamino hydroxamic acid derivatives
WO1996027583A1 (fr) 1995-03-08 1996-09-12 Pfizer Inc. Derives de l'acide arylsulfonylamino hydroxamique
US5861510A (en) 1995-04-20 1999-01-19 Pfizer Inc Arylsulfonyl hydroxamic acid derivatives as MMP and TNF inhibitors
WO1996033172A1 (fr) 1995-04-20 1996-10-24 Pfizer Inc. Derives d'acide hydroxamique arylsufonyle en tant qu'inhibiteurs de mmp et de tnf
WO1996040210A1 (fr) 1995-06-07 1996-12-19 Imclone Systems Incorporated Anticorps et fragments d'anticorps inhibant la croissance des tumeurs
WO1997022596A1 (fr) 1995-12-18 1997-06-26 Zeneca Limited Derives de quinazoline
EP0780386A1 (fr) 1995-12-20 1997-06-25 F. Hoffmann-La Roche Ag Inhibiteurs de métalloprotéases matricielles
US6258562B1 (en) 1996-02-09 2001-07-10 Basf Aktiengesellschaft Human antibodies that bind human TNFα
WO1997030035A1 (fr) 1996-02-13 1997-08-21 Zeneca Limited Derives de la quinazoline utilises comme inhibiteurs du vegf
WO1997032856A1 (fr) 1996-03-05 1997-09-12 Zeneca Limited Derives de 4-anilinoquinazoline
EP0818442A2 (fr) 1996-07-12 1998-01-14 Pfizer Inc. Dérivés cycliques de sulfones comme inhibiteurs de métalloprotéinase et de la production du facteur de nécrose des tumeurs
WO1998003516A1 (fr) 1996-07-18 1998-01-29 Pfizer Inc. Composes a base de phosphinate inhibiteurs des metalloproteases matricielles
WO1998007697A1 (fr) 1996-08-23 1998-02-26 Pfizer Inc. Derives de l'acide arylsulfonylamino hydroxamique
US6130237A (en) 1996-09-12 2000-10-10 Cancer Research Campaign Technology Limited Condensed N-aclyindoles as antitumor agents
WO1998013354A1 (fr) 1996-09-25 1998-04-02 Zeneca Limited Derives quinazolines et compositions pharmaceutiques les contenant
WO1998030566A1 (fr) 1997-01-06 1998-07-16 Pfizer Inc. Derives de sulfone cyclique
WO1998033768A1 (fr) 1997-02-03 1998-08-06 Pfizer Products Inc. Derives d'acide arylsulfonylaminohydroxamique
WO1998034915A1 (fr) 1997-02-07 1998-08-13 Pfizer Inc. Derives du n-hxdroxy-beta-sulfonyl-propionamide et leur utilisation comme inhibiteurs des metalloproteases matrices
WO1998034918A1 (fr) 1997-02-11 1998-08-13 Pfizer Inc. Derives de l'acide arylsulfonylhydroxamique
WO1998035985A1 (fr) 1997-02-12 1998-08-20 The Regents Of The University Of Michigan Proteines-marqueurs pour le cancer du poumon et utilisation de ces dernieres
US6239104B1 (en) 1997-02-25 2001-05-29 Arizona Board Of Regents Isolation and structural elucidation of the cytostatic linear and cyclo-depsipeptides dolastatin 16, dolastatin 17, and dolastatin 18
US6235883B1 (en) 1997-05-05 2001-05-22 Abgenix, Inc. Human monoclonal antibodies to epidermal growth factor receptor
WO1999007675A1 (fr) 1997-08-08 1999-02-18 Pfizer Products Inc. Derives de l'acide aryloxyarylsulfonylamino hydroxamique
WO1999029667A1 (fr) 1997-12-05 1999-06-17 Pfizer Limited Derives d'acide hydroxamique utilises comme inhibiteurs de metalloproteases matricielles
EP0931788A2 (fr) 1998-01-27 1999-07-28 Pfizer Limited Inhibiteurs de la métalloprotéinase
US6423685B1 (en) 1998-03-05 2002-07-23 Chiron Corporation Method for increasing the serum half-life of a biologically active molecule
EP0945864A2 (fr) 1998-03-26 1999-09-29 Sony Corporation Sélection de matériau vidéo
WO1999052910A1 (fr) 1998-04-10 1999-10-21 Pfizer Products Inc. Derives bicycliques de l'acide hydroxamique
WO1999052889A1 (fr) 1998-04-10 1999-10-21 Pfizer Products Inc. Hydroxamides de l'acide (4-arylsulfonylamino)-tetrahydropyrane-4-carboxylique
EP1004578A2 (fr) 1998-11-05 2000-05-31 Pfizer Products Inc. Dérivés d'hydroxamide de l'acide 5-oxo-pyrrolidine-2-carboxylique
WO2000034337A1 (fr) 1998-12-10 2000-06-15 Tsukuba Research Laboratory, Toagosei Co., Ltd. Anticorps monoclonaux humanises luttant contre un facteur de croissance de cellules endotheliales vasculaires
US6281211B1 (en) 1999-02-04 2001-08-28 Euro-Celtique S.A. Substituted semicarbazides and the use thereof
WO2000047212A1 (fr) 1999-02-10 2000-08-17 Astrazeneca Ab Derives de quinazoline utilises comme inhibiteurs de l'angiogenese
US6914128B1 (en) 1999-03-25 2005-07-05 Abbott Gmbh & Co. Kg Human antibodies that bind human IL-12 and methods for producing
US6323315B1 (en) 1999-09-10 2001-11-27 Basf Aktiengesellschaft Dolastatin peptides
WO2001032651A1 (fr) 1999-11-05 2001-05-10 Astrazeneca Ab Derives de quinazoline utilises en tant qu'inhibiteurs du facteur de croissance endotheliale vasculaire (vegf)
WO2001060814A2 (fr) 2000-02-15 2001-08-23 Sugen, Inc. Inhibiteurs de la proteine kinase 2-indolinone a substitution pyrrole
WO2001062931A2 (fr) 2000-02-25 2001-08-30 The Government Of The United States, As Represented By The Secretary Of The Department Of Health And Human Services SCFV ANTI-EGFRvIII POSSEDANT UNE CYTOTOXICITE ET UN RENDEMENT AMELIORES, IMMUNOTOXINES A BASE DE CES SCFV ET PROCEDE D'UTILISATION ASSOCIE
WO2001088138A1 (fr) 2000-05-19 2001-11-22 Scancell Limited Anticorps humanises contre le recepteur du facteur de croissance epidermique
US8258082B2 (en) 2000-12-18 2012-09-04 Dyax Corp. Focused libraries of genetic packages
WO2002085923A2 (fr) 2001-04-19 2002-10-31 The Scripps Research Institute Incorporation in vivo d'acides amines non naturels
US20030082575A1 (en) 2001-04-19 2003-05-01 The Scripps Research Institute In vivo incorporation of unnatural amino acids
US20030108885A1 (en) 2001-04-19 2003-06-12 The Scripps Research Institute Methods and compositions for the production of orthogonal tRNA-aminoacyltRNA synthetase pairs
US20050009751A1 (en) 2001-04-30 2005-01-13 Seattle Genetics, Inc. Pentapeptide compounds and uses related thereto
WO2002088172A2 (fr) 2001-04-30 2002-11-07 Seattle Genetics, Inc. Composes pentapeptidiques et leurs utilisations
US20030083263A1 (en) 2001-04-30 2003-05-01 Svetlana Doronina Pentapeptide compounds and uses related thereto
US7247301B2 (en) 2001-06-13 2007-07-24 Genmab A/S Human monoclonal antibodies to epidermal growth factor receptor (EGFR)
US20030143596A1 (en) 2001-11-07 2003-07-31 Shearwater Corporation Branched polymers and their conjugates
WO2003039486A2 (fr) 2001-11-09 2003-05-15 Idec Pharmaceuticals Corporation Anticorps anti-cd80 presentant une activite adcc visant la mort des cellules b de lymphome a mediation par adcc, isolement ou en combinaison avec d'autres therapies
EP1444268A2 (fr) 2001-11-12 2004-08-11 Gundram Jung Molecule d'anticorps anti-cd28 bispecifique
WO2004010957A2 (fr) 2002-07-31 2004-02-05 Seattle Genetics, Inc. Conjugues de medicaments et leur utilisation dans le traitement du cancer, d'une maladie auto-immune ou d'une maladie infectieuse
US20050238649A1 (en) 2003-11-06 2005-10-27 Seattle Genetics, Inc. Monomethylvaline compounds capable of conjugation to ligands
US20050147610A1 (en) 2003-11-12 2005-07-07 Tariq Ghayur IL-18 binding proteins
US7375078B2 (en) 2004-02-23 2008-05-20 Genentech, Inc. Heterocyclic self-immolative linkers and conjugates
WO2005111082A1 (fr) 2004-04-30 2005-11-24 Inserm (Institut National De La Sante Et De La Recherche Medicale) Anticorps anti-tfr
WO2006026306A1 (fr) 2004-08-31 2006-03-09 Biogen Idec Ma Inc. Pyrimidinylimidazoles utilises comme inhibiteurs de tgf-beta
US8431558B2 (en) 2004-11-01 2013-04-30 The Regents Of The University Of California Compositions and methods for modification of biomolecules
WO2007076127A2 (fr) 2005-12-22 2007-07-05 Biogen Idec Ma Inc Modulateurs du facteur de croissance transformant
WO2007076086A2 (fr) 2005-12-22 2007-07-05 Biogen Idec Ma Inc Modulateurs du facteur de croissance transformant
WO2007124299A2 (fr) 2006-04-21 2007-11-01 Novartis Ag Compositions pharmaceutiques d'anticorps anti-cd40 antagoniste
US20140249135A1 (en) 2007-03-01 2014-09-04 Novartis Ag Pim kinase inhibitors and methods of their use
WO2009009059A1 (fr) 2007-07-09 2009-01-15 Biogen Idec Ma Inc. Composés spiro en tant qu'antagonistes du tgf-bêta
US8691730B2 (en) 2007-09-14 2014-04-08 Adimab, Llc Rationally designed, synthetic antibody libraries and uses therefor
US20100137386A1 (en) 2008-12-01 2010-06-03 Tesshi Yamada Tnik inhibitor and the use
US20100216795A1 (en) 2008-12-01 2010-08-26 Tesshi Yamada Tnik inhibitor and the use
US8703936B2 (en) 2010-02-12 2014-04-22 The Regents Of The University Of California Compositions and methods for modification of biomolecules
US9222940B2 (en) 2010-04-27 2015-12-29 Synaffix B.V. Fused cyclooctyne compounds and their use in metal-free click reactions
US8080568B1 (en) 2010-06-29 2011-12-20 Ewha University - Industry Collaboration Foundation 2-pyridyl substituted imidazoles as therapeutic ALK5 and/or ALK4 inhibitors
WO2012002680A2 (fr) 2010-06-29 2012-01-05 Ewha University-Industry Collaboration Foundation Imidazoles à substitution 2-pyridyle comme inhibiteurs thérapeutiques de l'alk5 et/ou de l'alk4
US20120225061A1 (en) 2011-03-04 2012-09-06 Matthew Burger Tetrasubstituted cyclohexyl compounds as kinase inhibitors
US9145361B2 (en) 2011-03-25 2015-09-29 Life Technologies Corporation SDP-containing heterobifunctional agents
US20130251783A1 (en) 2011-09-14 2013-09-26 Universitat Heidelberg Liposomes containing permeation enhancers for oral drug delivery
US20130189287A1 (en) 2011-12-23 2013-07-25 Paul Scherrer Institut Enzymatic conjugation of polypeptides
US20140356385A1 (en) 2011-12-23 2014-12-04 Innate Pharma Enzymatic conjugation of antibodies
US20150045368A1 (en) 2012-03-05 2015-02-12 Amgen Inc. Oxazolidinone compounds and derivatives thereof
WO2013185115A1 (fr) 2012-06-08 2013-12-12 Sutro Biopharma, Inc. Anticorps comprenant des résidus d'acides aminés non endogènes spécifiques d'un site, leurs procédés de préparation et leurs procédés d'utilisation
US9738724B2 (en) * 2012-06-08 2017-08-22 Sutro Biopharma, Inc. Antibodies comprising site-specific non-natural amino acid residues, methods of their preparation and methods of their use
WO2014036022A1 (fr) 2012-08-29 2014-03-06 Amgen Inc. Composés quinazolinones et leurs dérivés
US9505749B2 (en) 2012-08-29 2016-11-29 Amgen Inc. Quinazolinone compounds and derivatives thereof
WO2015006555A2 (fr) 2013-07-10 2015-01-15 Sutro Biopharma, Inc. Anticorps comprenant plusieurs résidus d'acides aminés non naturels site-spécifiques, des procédés permettant leur préparation et leurs méthodes d'utilisation
US20160264555A1 (en) 2013-12-06 2016-09-15 National Cancer Center Novel quinazoline derivative
WO2015083833A1 (fr) 2013-12-06 2015-06-11 カルナバイオサイエンス株式会社 Nouveau dérivé quinazoline
WO2015136073A1 (fr) 2014-03-14 2015-09-17 Oncodesign Sa Inhibiteurs macrocycliques de la kinase tgf-br2
WO2016020864A1 (fr) 2014-08-06 2016-02-11 Novartis Ag Inhibiteurs de protéine kinase c et leurs procédés d'utilisation
WO2016123582A1 (fr) 2015-01-30 2016-08-04 Sutro Biopharma, Inc. Dérivés d'hémiasterline pour conjugaison et thérapie
US20180127426A1 (en) 2015-03-02 2018-05-10 Rigel Pharmaceuticals, Inc. TGF-Beta Inhibitors
EP3313177A1 (fr) 2015-06-26 2018-05-02 Zobele Holding SpA Dispositif permettant de piéger des insectes
WO2017076484A1 (fr) 2015-11-02 2017-05-11 Merck Patent Gmbh Dérivés de 1,4-dicarbonyle-pipéridyle
CN107226808A (zh) 2016-03-23 2017-10-03 山东轩竹医药科技有限公司 端锚聚合酶抑制剂
WO2018003962A1 (fr) 2016-06-30 2018-01-04 国立研究開発法人理化学研究所 Nouveau composé ou son sel pharmaceutiquement accepté
WO2018046933A1 (fr) 2016-09-08 2018-03-15 University Of Bath Inhibiteurs de tankyrase
US10596270B2 (en) 2017-09-18 2020-03-24 Sutro Biopharma, Inc. Anti-folate receptor antibody conjugates, compositions comprising anti-folate receptor antibody conjugates, and methods of making and using anti-folate receptor antibody conjugates
WO2020252015A1 (fr) 2019-06-10 2020-12-17 Sutro Biopharma, Inc. Conjugués anticorps-médicament immunomodulateurs et utilisations associées
US20240261426A1 (en) * 2021-06-28 2024-08-08 Byondis B.V. Conjugates comprising phosphoantigens and their use in therapy
WO2023207710A1 (fr) * 2022-04-29 2023-11-02 四川科伦博泰生物医药股份有限公司 Conjugué anticorps-médicament, composition pharmaceutique de celui-ci et son utilisation
WO2024006272A1 (fr) 2022-06-27 2024-01-04 Sutro Biopharma, Inc. CHARGES UTILES DE LIEUR β-GLUCURONIDE, LEURS CONJUGUÉS PROTÉIQUES ET MÉTHODES ASSOCIÉES
WO2024006542A1 (fr) * 2022-06-30 2024-01-04 Sutro Biopharma, Inc. Anticorps anti-ror1 et conjugués d'anticorps, compositions comprenant des anticorps anti-ror1 ou des conjugués d'anticorps, et méthodes de fabrication et d'utilisation d'anticorps anti-ror1 et de conjugués d'anticorps
EP4410313A1 (fr) * 2023-01-31 2024-08-07 Synaffix B.V. Conjugués d'anticorps homogènes à charge utile élevée

Non-Patent Citations (109)

* Cited by examiner, † Cited by third party
Title
"Handbook of Pharmaceutical Excipients", 2009, THE PHARMACEUTICAL PRESS
"Quisqualic acid analogues: synthesis of beta-heterocyclic 2-aminopropanoic acid derivatives and their activity at a novel quisqualate-sensitized site", J. MED. CHEM., vol. 35, 1992, pages 4602 - 7
"The Pharmacology of Monoclonal Antibodies", vol. 113, SPRINGER-VERLAG, article "Antibodies from Escherichia coli.", pages: 269 - 315
ABHINANDANMARTIN, IMMUNOLOGY, vol. 45, 2008, pages 3832 - 3839
ACTA CRYST., no. D72, 2016, pages 658 - 674
AL-LAZIKANI ET AL., J. MOL. BIOL., vol. 273, 1997, pages 927 - 948
AMSBERRY ET AL., J. ORG. CHEM., vol. 55, 1990, pages 5867
ANGEW CHEM. INTL. ED. ENGL., vol. 33, 1994, pages 183 - 186
AZOULAY, M.VILMONT, M.FRAPPIER, F.: "Glutamine analogues as Potential Antimalarials", EUR. J. MED. CHEM., vol. 26, 1991, pages 201 - 5
BARBAS ET AL., PROC. NAT. ACAD. SCI. U.S.A., vol. 91, 1994, pages 3809 - 3813
BARNES ET AL., ANAL. BIOCHEM.,, vol. 102, 1980, pages 255
BARTON ET AL.: "Synthesis of Novel a-Amino-Acids and Derivatives Using Radical Chemistry: Synthesis of L- and D-a-Amino-Adipic Acids, L-a-aminopimelic Acid and Appropriate Unsaturated Derivatives", TETRAHEDRON LETT., vol. 43, pages 4297 - 4308
BHAGCHANDANI ET AL., ADVANCED DRUG DELIVERY REVIEWS, vol. 175, 2021, pages 113803
BIOORG. MED. CHEM. LETT., vol. 23, 2013, pages 3248 - 3252
BIOORG. MED. CHEM. LETT., vol. 9, 1999, pages 2237
BIOORG. MED. CHEM., vol. 22, 2014, pages 2724 - 2732
BRUGGEMANNTAUSSIG, CURR. OPIN. BIOTECHNOL., vol. 8, 1997, pages 455 - 458
BRUGGERMANN ET AL., YEAR IN IMMUNO., vol. 7, 1993, pages 33
BURROWS ET AL.: "Association of asthma with serum IgE levels and skin-test reactivity to allergens", NEW ENGL. L. MED., vol. 320, 1989, pages 271 - 277
CAREYSUNDBERG: "Advanced Organic Chemistry", 1990, WILEY AND SONS
CHARI ET AL., CANCER RES., vol. 52, 1992, pages 127 - 131
CHIN J. ET AL., SCIENCE, vol. 301, 2003, pages 964 - 7
CHIN, J. W. ET AL., J. AM. CHEM. SOC., vol. 124, 2002, pages 9026 - 9027
CHRISTIE, B. D.RAPOPORT, H.: "Synthesis of Optically Pure Pipecolates from L-Asparagine", J. ORG. CHEM., 1985, pages 1859 - 1866
CLARK, IMMUNOL. TODAY, vol. 21, 2000, pages 397 - 402
CORNISH, V. W. ET AL., J. AM. CHEM. SOC., vol. 118, 1996, pages 8150 - 8151
CRAIG, J. C. ET AL.: "Absolute Configuration of the Enantiomers of 7-Chloro-4 [[4-(diethylamino)-1-methylbutyl]amino]quinoline (Chloroquine", J. ORG. CHEM., vol. 53, 1988, pages 1167 - 1170
DEITERS, A. ET AL., J. AM. CHEM. SOC., vol. 125, 2003, pages 11782 - 11783
E. SAXONC. BERTOZZI, SCIENCE, vol. 287, 2000, pages 2007 - 2010
ECKER ET AL., MABS, vol. 7, no. 1, 2015, pages 9 - 14
EUR. J. MED. CHEM., vol. 142, 2017, pages 506 - 522
EVANS ET AL., ACS OMEGA, vol. 4, no. 13, 2019, pages 15665
FANGER, M W ET AL., CRIT REV IMMUNOL., vol. 12, no. 34, 1992, pages 101 - 24
FOSTER ET AL., ADV. DRUG RES., vol. 14, 1985, pages 1 - 36
FRIEDMAN, O. M.CHATTERRJI, R.: "Synthesis of Derivatives of Glutamine as Model Substrates for Anti-Tumor Agents", J. AM. CHEM. SOC., vol. 81, 1959, pages 3750 - 3752
GATELY ET AL., J. NUCL. MED., vol. 27, 1986, pages 388
GEOGHEGAN, K. F.STROH, J. G., BIOCONJUG. CHEM., vol. 3, 1992, pages 138 - 146
GORDON ET AL., DRUG METAB. DISPOS., vol. 15, pages 589
GRIFFITHSDUNCAN, CURR. OPIN. BIOTECHNOL., vol. 9, 1998, pages 102 - 108
GUSS ET AL., EMBO J., vol. 5, 1986, pages 1567 - 1575
H. HANGC. BERTOZZI, ACC. CHEM. RES., vol. 34, 2001, pages 727 - 736
HAM ET AL., METH. ENZ., vol. 58, 1979, pages 44
HAMANN ET AL., EXPERT OPIN. THER. PATENTS, vol. 15, 2005, pages 1087 - 1103
HAWKINS ET AL., J. MOL. BIOL., vol. 226, 1992, pages 889 - 896
HONEGGEPLUCKTHUN, J. MOL. BIOL., vol. 309, 2001, pages 657 - 70
HOOGENBOOM ET AL., J. MOL. BIOL., vol. 222, 1991, pages 581 - 597
INT. J. CANCER, vol. 105, no. 2, 2003, pages 273 - 80
J. MED. CHEM., vol. 38, 1995, pages 4660 - 4669
J. MED. CHEM., vol. 57, 2014, pages 4213 - 4238
JACKSON ET AL., J. IMMUNOL., vol. 154, 1995, pages 3310 - 33199
JAKOBOVITS ET AL., NATURE, vol. 362, 1993, pages 255 - 258
JAKOBOVITS ET AL., PROC. NATL. ACAD. SCI. U.S.A., vol. 90, 1993, pages 2551
JENCKS, W. P., J. AM. CHEM. SOC., vol. 81, 1959, pages 475 - 481
JONES ET AL., NATURE, vol. 321, 1986, pages 522 - 525
JOURNAL OF BIOLOGICAL CHEMISTRY
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
JUNGBLUTH ET AL., PROC. NATL. ACAD. SCI. USA., vol. 100, no. 2, 2003, pages 639 - 44
KABATCHOTHIA: "Antibody Engineering", vol. 2, 2010, SPRINGER-VERLAG, article "Protein Sequence and Structure Analysis of Antibody Variable Domains", pages: 33 - 51
KAYSER, B. ET AL., TETRAHEDRON, vol. 53, no. 7, 1997, pages 2475 - 2484
KETTLEBOROUGH ET AL., PROTEIN ENG., vol. 4, no. 7, 1991, pages 773 - 83
KIICK ET AL.: "Incorporation of azides into recombinant proteins for chemoselective modification by the Staudinger ligation", PNAS, vol. 99, 2002, pages 19 - 24
KING, F. E.KIDD, D. A. A.: "A New Synthesis of Glutamine and of -Dipeptides of Glutamic Acid from Phthylated Intermediates", J. CHEM. SOC., 1949, pages 3315 - 3319
KING, M.WAGNER, A: "Developments in the Field of Bioorthogonal Bond Forming Reactions - Past and Present Trends", BIOCONJUGATE CHEM., vol. 25, no. 5, 2014, pages 825 - 839
KINGSBURY ET AL., J. MED. CHEM., vol. 27, 1984, pages 1447
KOHLER ET AL., NATURE, vol. 256, 1975, pages 495 - 497
KOSKINEN, A. M. P.RAPOPORT, H.: "Synthesis of 4-Substituted Prolines as Conformationally Constrained Amino Acid Analogues", J. ORG. CHEM., vol. 54, 1989, pages 1859 - 1866
KOZBOR, J. IMMUNOL., vol. 133, 1984, pages 3001 - 176
KUSHNER ET AL., CAN. J. PHYSIOL. PHARMACOL., vol. 77, 1999, pages 79 - 88
KYOJI TSUCHIKAMA ET AL: "Antibody-drug conjugates: recent advances in conjugation and linker chemistries", PROTEIN & CELL, vol. 9, no. 1, 14 October 2016 (2016-10-14), Beijing, CN, pages 33 - 46, XP055461467, ISSN: 1674-800X, DOI: 10.1007/s13238-016-0323-0 *
LANG, K.CHIN, J.: "Bioorthogonal Reactions for Labeling Proteins", ACS CHEM BIOL, vol. 9, 2014, pages 16 - 20
LEFRANC ET AL., DEV. COMP. IMMUNOL., vol. 27, 2003, pages 55 - 77
LIJINSKY ET AL., FOOD COSMET. TOXICOL., vol. 20, 1982, pages 393
LIJINSKY ET AL., J. NAT. CANCER INST., vol. 69, 1982, pages 1127 - 161
LINDMARK ET AL., J. IMMUNOL. METH., vol. 62, 1983, pages 1 - 13
LUDWIG, INSTITUTE FOR CANCER RESEARCH, MEMORIAL SLOAN-KETTERING
M. CARRASCOR. BROWN, J. ORG. CHEM., vol. 68, 2003, pages 8853 - 8858
MACCALLUM ET AL., J. MOL. BIOL., vol. 262, 1996, pages 732 - 745
MAHAL, L. K. ET AL., SCIENCE, vol. 276, 1997, pages 1125 - 1128
MANGOLD ET AL., MUTATION RES., vol. 308, 1994, pages 33
MARKS ET AL., BIO/TECHNOLOGY, vol. 10, 1992, pages 163 - 167
MATEO ET AL., IMMUNOTECHNOL, vol. 3, no. 1, 1997, pages 71 - 81
MED. CHEM. COMMUN., vol. 6, 2015, pages 1564 - 1572
MODJTAHEDI ET AL., BR. J. CANCER, vol. 67, no. 2, 1993, pages 247 - 53
MODJTAHEDI ET AL., BR. J. CANCER, vol. 73, no. 2, 1996, pages 228 - 35
MODJTAHEDI ET AL., J. CELL. BIOPHYS., vol. 22, 1993, pages 129 - 46
MURTHY ET AL., ARCH. BIOCHEM. BIOPHYS., vol. 252, no. 2, 1987, pages 549 - 60
NOLAN, O, R. O'KENNEDY, BIOCHIM BIOPHYS ACTA, vol. 1, no. 1, August 1990 (1990-08-01), pages 1 - 11
PADWA, A.: "COMPREHENSIVE ORGANIC SYNTHESIS", vol. 4, 1991, pages: 1069 - 1109
PATERSON, D. M. ET AL.: "Finding the Right (Bioorthogonal) Chemistry", ACS CHEM BIOL, vol. 9, 2014, pages 592 - 605
PRESTA, CURR. OP. STRUCT. BIOL., vol. 2, 1992, pages 593 - 596
PRESTA, L. G, J. ALLERGY CLIN. IMMUNOL., vol. 116, 2005, pages 731 - 6
QUEEN ET AL., PROC. NATL. ACAD. SCI. U.S.A., vol. 86, 1989, pages 10029 - 10033
RADER ET AL., PROC. NAT. ACAD. SCI. U.S.A., vol. 95, 1998, pages 8910 - 8915
RAMIL, C.P.LIN, Q.: "Bioorthogonal chemistry: strategies and recent developments", CHEM COMMUN, vol. 49, 2013, pages 11007 - 11022
RIECHMANN ET AL., NATURE, vol. 332, 1988, pages 323 - 329
RODECK ET AL., CELL. BIOCHEM., vol. 35, no. 4, 1987, pages 315 - 20
RODRIGUES ET AL., CHEMISTRY BIOLOGY, vol. 2, 1995, pages 223
ROSENTHAL, G. ET AL., LIFE SCI., vol. 60, 1997, pages 1635 - 1641
ROSTOVTSEV ET AL., ANGEW. CHEM. INT. ED., vol. 41, 2002, pages 2596 - 2599
SCHIER ET AL., GENE, vol. 169, 1995, pages 147 - 155
SHAO, J.TAM, J. P, J. AM. CHEM. SOC., vol. 117, no. 14, 1995, pages 3893 - 3899
STEINBERGER ET AL., J. BIOL. CHEM., vol. 275, 2000, pages 36073 - 36078
STORM ET AL., J. AMER. CHEM. SOC., vol. 94, 1972, pages 5815
TORNOE, C. W. ET AL., J. ORG. CHEM., vol. 67, 2002, pages 3057 - 3064
WADE D, CHEM. BIOL. INTERACT., vol. 117, 1999, pages 191
WINTERMILSTEIN, NATURE, vol. 349, 1991, pages 293 - 299
WOLFF, A C ET AL., J CLIN ONCOL., vol. 31, no. 31, 1 November 2013 (2013-11-01), pages 3997 - 4013
YIN ET AL., MABS, vol. 4, 2012, pages 217 - 225
ZELLO ET AL., METABOLISM, vol. 43, 1994, pages 487

Similar Documents

Publication Publication Date Title
US20240139285A1 (en) Immunomodulator antibody drug conjugates and uses thereof
US20250236594A1 (en) Modified amino acids
US12534465B2 (en) 5H-pyrrolo[3,2-d]pyrimidine-2,4-diamino compounds and antibody conjugates thereof
US10442789B2 (en) Modified amino acids comprising tetrazine functional groups, methods of preparation, and methods of their use
ES2658039T3 (es) Anticuerpos que comprenden múltiples residuos de aminoácidos no naturales sitio-específicos, métodos para su preparación y métodos de uso
US20220259202A1 (en) 1-(4-(aminomethyl)benzyl)-2-butyl-2h-pyrazolo[3,4-c]quinolin-4-amine derivatives and related compounds as toll-like receptor (tlr) 7/8 agonists, as well as antibody drug conjugates thereof for use in cancer therapy and diagnosis
KR20250043602A (ko) 항-ror1 항체 및 항체 접합체, 항-ror1 항체 또는 항체 접합체를 포함하는 조성물, 및 항-ror1 항체 및 항체 접합체의 제조 및 사용 방법
WO2025080711A9 (fr) Conjugués médicament-anticorps à double charge utile
WO2026080697A1 (fr) Conjugués d'anticorps à rapports élevés charge utile/anticorps, compositions les comprenant, et leurs procédés d'utilisation
WO2026080688A1 (fr) Conjugués anticorps-médicament à charge utile à double mécanisme d'action
WO2026043823A2 (fr) Anticorps comprenant des résidus d'acides aminés non naturels spécifiques à un site, leurs procédés de préparation et leurs utilisations
HK1210034B (en) Modified amino acids comprising an azido group