SELECTED PUBLICATIONS

Brentuximab vedotin (SGN-35) AND CD30-RELATED

Intracellular activation of SGN-35, a potent anti-CD30 antibody-drug conjugate
Okeley, N.M., et.al.
Clinical Cancer Research, 2010, 16(3):888-897

The antibody-drug conjugate brentuximab vedotin (SGN-35) induced multiple objective responses in patients with relapsed or refractory CD30-positive lymphomas in a phase 1 weekly dosing study
Fanale, M., et.al.
American Society of Hematology 2009 Annual Meeting (abstract # 2731)

Robust antitumor activity of the antibody-drug conjugate SGN-35 when administered every 3 weeks to patients with relapsed or refractory CD30-positive hematologic malignancies in a phase I study
Younes, A., et.al.
European Hematology Association 2009 Congress (abstract # 503)

Complete remissions with SGN-35 weekly dosing: a phase I dose-escalation study in relapsed/refractory Hodgkin lymphoma or systemic ALCL patients
Bartlett, N.L., et.al.
American Society of Clinical Oncology 2009 Annual Meeting (abstract # 8500)

Antibody-targeted delivery of auristatin with SGN-35 is superior to non-targeted therapy
Alley, S.C., et.al.
American Association for Cancer Research 2009 Annual Meeting (abstract #3234)

Multiple complete responses in a phase I dose-escalation study of the antibody-drug conjugate SGN-35 in patients with relapsed or refractory CD30-positive lymphomas
Younes, A., et.al.
American Society of Hematology 2008 Annual Meeting (abstract #1006)

Combination of the anti-CD30-auristatin-E antibody-drug conjugate (SGN-35) with chemotherapy improves antitumor activity in Hodgkin lymphoma
Oflazoglu, E., et.al.
British Journal of Haematology, 2008, 142(1):69-73

CD30 expression on CD1a+ and CD8+ cells in atopic dermatitis and correlation with disease severity
Oflazoglu, E., et.al.
European Journal of Dermatology, 2008, 18(1):41-9

Lysosomal trafficking and cysteine protease metabolism confer target-specific cytotoxicity by peptide-linked anti-CD30-auristatin conjugates
Sutherland, M.S.K., et.al.
Journal of Biological Chemistry, 2006, 281(15):10540-7

In vivo drug-linker stability of an anti-CD30 dipeptide-linked auristatin immunoconjugate
Sanderson, R.J., et.al.
Clinical Cancer Research 2005, 11(2 Pt 1):843-52

cAC10-vcMMAE, an anti-CD30-monomethyl auristatin E conjugate with potent and selective antitumor activity
Francisco, J.A., et.al.
Blood, 2003, 102(4):1458-65

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Antibody-Drug Conjugate (ADC) Technology

Development of parallel conjugation and assay methodologies to screen for antibodies with optimal properties for use as antibody-drug conjugates
Lyon, R.P.,et.al.
American Association for Cancer Research 2010 Annual Meeting (abstract # 4394)

Contribution of linker stability to the activities of anticancer immunoconjugates
Alley, S.C.,et.al.
Bioconjugate Chemistry, 2008, 19(3):759-65

Novel peptide linkers for highly potent antibody-auristatin conjugate
Doronina, S.O., et.al.
Bioconjugate Chemistry, 2008, 19(10):1960-3

Enhanced activity of monomethylauristatin F through monoclonal antibody delivery: effects of linker technology on efficacy and toxicity
Doronina, S.O., et.al.
Bioconjugate Chemistry, 2006, 17(1):114-24

Reduction-alkylation strategies for the modification of specific monoclonal antibody disulfides
Sun, M.M.C., et.al.
Bioconjugate Chemistry, 2005, 16(5):1282-90

Arming antibodies: prospects and challenges for immunoconjugates
Wu, A.M., Senter, P.D.
Nature Biotechnology, 2005, 23(9):1137-46

Effects of drug loading on the antitumor activity of a monoclonal antibody-drug conjugate
Hamblett, K.J., et.al.
Clinical Cancer Research, 2004, 10(20):7063-70

Secondary mAb-vcMMAE conjugates are highly sensitive reporters of antibody internalization via the lysosome pathway
Klussman, K., et.al.
Bioconjugate Chemistry, 2004, 15(4):765-73

Development of potent monoclonal antibody auristatin conjugates for cancer therapy
Doronina, S.O., et.al.
Nature Biotechnology, 2003, 21(7):778-84

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Lintuzumab (SGN-33) AND CD33-RELATED

Complete remissions observed in acute myeloid leukemia following prolonged exposure to lintuzumab: a phase 1 trial
Raza, A., et.al.
Leukemia & Lymphoma, 2009, 50:8, 1336-1344

Anti-leukemic activity of lintuzumab (SGN-33) in preclinical models of acute myeloid leukemia
Sutherland, M.S.K., et.al.
mAbs, 2009, 1:5, 481-490

Prolonged exposure to lintuzumab monotherapy in acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS) - results of a phase I trial
Raza, A., et.al.
European Hematology Association 2009 Congress (abstract # 983)

SGN-33, lintuzumab, demonstrates anti-leukemic activity in MDR-positive preclinical models of AML
Sutherland, M.S.K., et.al.
American Association for Cancer Research 2008 Annual Meeting (abstract #1513)

Complete remissions observed in acute myeloid leukemia following prolonged exposure to SGN-33 (lintuzumab), a humanized monoclonal antibody targeting CD33
Raza, A., et.al.
American Society of Hematology 2007 Annual Meeting (abstract #159)

SGN-33 (lintuzumab) demonstrates anti-leukemic activity in preclinical models of AML
Sutherland, M.S.K., et.al.
American Society of Hematology 2007 Annual Meeting (abstract #919)

SGN-33 (lintuzumab) a humanized anti-CD33 antibody, modulates the activity of CD30-positive tumor- associated macrophages
Sutherland, M.S.K., et.al.
American Association for Cancer Research 2007 Annual Meeting (abstract #4111)

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Dacetuzumab (SGN-40) and CD40-related

A phase 1b clinical trial of dacetuzumab in combination with rituximab and gemcitabine: multiple responses observed in patients with relapsed diffuse large B-cell lymphoma
Forero-Torres, A., et.al.
American Society of Hematology 2009 Annual Meeting (abstract # 586)

Dacetuzumab (SGN-40), lenalidomide, and weekly dexamethasone in relapsed or refractory multiple myeloma: multiple responses observed in a phase 1b study
Agura, E., et.al.
American Society of Hematology 2009 Annual Meeting (abstract # 2870)

Phase I study of the humanized anti-CD40 monoclonal antibody dacetuzumab in refractory or recurrent non-Hodgkin's lymphoma
Advani, R., et.al.
Journal of Clinical Oncology, 2009, 27(26):4371-7

Dacetuzumab (SGN-40), a humanized anti-CD40 monoclonal antibody, has chemosensitization activity and improves gemcitabine efficacy in NHL xenograft models
Lewis, T.S., et.al.
American Association for Cancer Research 2009 Annual Meeting (abstract #3243)

A gene signature predicts sensitivity to the partial CD40 agonist, dacetuzumab (SGN-40), in patients with diffuse large B-cell lymphoma
Burington, B., et.al.
American Association for Cancer Research 2009 Annual Meeting (abstract #LB-138)

Macrophages and Fc-receptor interactions contribute to the antitumour activities of the anti-CD40 antibody SGN-40
Oflazoglu, E., et.al.
British Journal of Cancer, 2009, 100(1):113-7

A phase 2 clinical trial of SGN-40 (dacetuzumab) monotherapy in relapsed diffuse large B-cell lymphoma
Advani, R., et.al. American Society of Hematology 2008 Annual Meeting (abstract #1000)

Preclinical analysis of the combined activity of SGN-40 (dacetuzumab), anti-CD40 monoclonal antibody, with rituximab in non-Hodgkin lymphoma
Lewis, T.S., et.al.
American Society of Hematology 2008 Annual Meeting (abstract # 1583)

SGN-40 shows evidence of activity in patients with relapsed non-Hodgkin's lymphoma: final results of a phase 1 dose-escalation study
Advani, R., et.al.
International Conference on Malignant Lymphoma, 2008

The humanized anti-CD40 monoclonal antibody, SGN-40, potentiates chemotherapy regimens in NHL xenograft models via proapoptotic signaling
Lewis, T.S., et.al.
American Society of Hematology 2007 Annual Meeting (abstract #2342)

Preclinical antilymphoma activity of a humanized anti-CD40 monoclonal antibody, SGN-40
Law, C.L., et.al.
Cancer Research; 2005, 65(18):8331-8

Immunomodulatory drug lenalidomide (CC-5013, IMiD3) augments anti-CD40 SGN-40-induced cytotoxicity in human multiple myeloma: clinical implications
Tai, Y.T., et.al.
Cancer Research, 2005, 65(24):11712-20

Mechanisms by which SGN-40, a humanized anti-CD40 antibody, induces cytotoxicity in human multiple myeloma cells: clinical implications
Tai, Y.T., et.al.
Cancer Research, 2004, 64(8):2846-52

Recombinant humanized anti-CD40 monoclonal antibody triggers autologous antibody-dependent cell-mediated cytotoxicity against multiple myeloma cells
Hayashi, T., et.al.
British Journal of Haematology, 2003, 121(4):592-6

Activation-induced cell death of aggressive histology lymphomas by CD40 stimulation: induction of bax
Szocinski, J.L., et.al.
Blood, 2002, 100(1):217-23

Agonistic properties and in vivo antitumor activity of the anti-CD40 antibody SGN-14
Francisco, J.A., et.al.
Cancer Research, 2000, 60(12):3225-31

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SGN-70

Blocking of CD27/CD70 pathway by anti-CD70 antibody ameliorates joint disease in murine collagen-induced arthritis
Oflazoglu, E., et.al.
Journal of Immunology, 2009, 183: 3770-3777

Targeting CD70 for the treatment of autoimmune disorders
McEarchern, J.A., et.al.
American College of Rheumatology, 2008 Annual Scientific Meeting

Immune modulation mediated by the humanized anti-CD70 monoclonal antibody SGN-70
Klussman, K., et.al.
American Association of Immunologists / Experimental Biology 2008 Annual Meeting (abstract #LB-457)

Preclinical characterization of SGN-70, a humanized antibody directed against CD70
McEarchern, J.A., et.al.
Clinical Cancer Research, 2008, 14(23):7763-72

Engineered anti-CD70 antibody with multiple effector functions exhibits in vitro and in vivo antitumor activities
McEarchern, J.A., et.al.
Blood, 2007, 109(3):1185-92

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SGN-75 AND CD70-RELATED

Mechanism of cysteine-mcMMAF release from the antibody-drug conjugate SGN-75
Zhang, X., et.al.
American Association for Cancer Research 2010 Annual Meeting (abstract #5334)

CD70 expression in multiple types of carcinomas: new targets for auristatin-based anti-CD70 antibody-drug conjugate SGN-75
Smith, L.M., et.al.
American Association for Cancer Research 2009 Annual Meeting (abstract #4652)

The pharmacologic basis for antibody-auristatin conjugate activity
Alley, S.C., et.al.
Journal of Pharmacology and Experimental Therapeutics, 2009, 330:932-938

Potent anticarcinoma activity of the humanized anti-CD70 antibody h1F6 conjugated to the tubulin inhibitor auristatin via an uncleavable linker
Oflazoglu, E., et.al.
Clinical Cancer Research, 2008, 14(19):6171-80

Biodistribution of a dual labeled anti-CD70 auristatin antibody-drug conjugate in tumor-bearing mice: experimental and modeled data
Alley, S.C., et.al.
American Association for Cancer Research 2008 Annual Meeting (abstract #4063)

Potent anticarcinoma activity of the anti-CD70 antibody h1F6 conjugated to the tubulin inhibitor auristatin via an uncleavable linker
Oflazoglu, E., et.al.
American Association for Cancer Research 2008 Annual Meeting (abstract #4064)

Effects of linker chemistry on tumor targeting by anti-CD70 antibody-drug conjugates
Alley, S.C., et.al.
American Association for Cancer Research 2007 Annual Meeting (abstract #916)

Lymphocyte activation antigen CD70 expressed by renal cell carcinoma is a potential therapeutic target for anti-CD70 antibody-drug conjugates
Law, C.L., et.al.
Cancer Research, 2006, 66(4):2328-37

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ASG-5ME

Preclinical evaluation of ASG-5ME, a novel antibody-drug conjugate for pancreatic cancer
Smith, L.M., et.al.
American Association for Cancer Research 2010 Annual Meeting (abstract #2590)

ASG-5ME is a novel antibody drug conjugate (ADC) for treating prostate cancers
Gudas, J.M. et.al.
American Association for Cancer Research 2010 Annual Meeting (abstract #4393)

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