Search Results - "Hamann, Philip R."

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    Selection of Reaction Additives Used in the Preparation of Monomeric Antibody−Calicheamicin Conjugates by Hollander, Irwin, Kunz, Arthur, Hamann, Philip. R

    Published in Bioconjugate chemistry (01-01-2008)
    “…The formation of protein aggregates can be a major problem during the preparation of antibody−drug conjugates. Herein is described the methods by which…”
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    Potent and Specific Antitumor Efficacy of CMC-544, a CD22-Targeted Immunoconjugate of Calicheamicin, against Systemically Disseminated B-Cell Lymphoma by DIJOSEPH, John F, GOAD, Mary E, DOUGHER, Maureen M, BOGHAERT, Erwin R, KUNZ, Arthur, HAMANN, Philip R, DAMLE, Nitin K

    Published in Clinical cancer research (15-12-2004)
    “…Purpose: CMC-544 is a CD22-targeted immunoconjugate of calicheamicin and exerts a potent cytotoxic effect against CD22 + B-cell lymphoma. This study evaluated…”
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    CD20-specific antibody-targeted chemotherapy of non-Hodgkin's B-cell lymphoma using calicheamicin-conjugated rituximab by Dijoseph, John F, Dougher, Maureen M, Armellino, Douglas C, Kalyandrug, Lyka, Kunz, Arthur, Boghaert, Erwin R, Hamann, Philip R, Damle, Nitin K

    Published in Cancer Immunology, Immunotherapy (01-07-2007)
    “…Tumor-targeted delivery of a potent cytotoxic agent, calicheamicin, using its immunoconjugates is a clinically validated therapeutic strategy. Rituximab is a…”
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    Syntheses and EGFR kinase inhibitory activity of 6-substituted-4-anilino [1,7] and [1,8] naphthyridine-3-carbonitriles by Wissner, Allan, Hamann, Philip R., Nilakantan, Ramaswamy, Greenberger, Lee M., Ye, Fei, Rapuano, Timothy A., Loganzo, Frank

    Published in Bioorganic & medicinal chemistry letters (22-03-2004)
    “…The syntheses and EGFR kinase inhibitory activity of a series of 6-substituted-4-anilino [1,7] and [1,8] naphthyridine-3-carbonitriles are described. Both…”
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    An Anti-CD33 Antibody−Calicheamicin Conjugate for Treatment of Acute Myeloid Leukemia. Choice of Linker by Hamann, Philip R, Hinman, Lois M, Beyer, Carl F, Lindh, Delores, Upeslacis, Janis, Flowers, David A, Bernstein, Irwin

    Published in Bioconjugate chemistry (01-01-2002)
    “…The anti-CD33 antibody, P67.6, has been chosen to target the potently cytotoxic calicheamicin antitumor antibiotics to acute myeloid leukemia (AML) due to the…”
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    An Anti-MUC1 Antibody−Calicheamicin Conjugate for Treatment of Solid Tumors. Choice of Linker and Overcoming Drug Resistance by Hamann, Philip R, Hinman, Lois M, Beyer, Carl F, Greenberger, Lee M, Lin, Clara, Lindh, Delores, Menendez, Ana T, Wallace, Rosalyn, Durr, Frederick E, Upeslacis, Janis

    Published in Bioconjugate chemistry (01-03-2005)
    “…The anti-MUC1 antibody, CTM01, has been chosen to target the potently cytotoxic calicheamicin antitumor antibiotics to solid tumors of epithelial origin that…”
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    A Calicheamicin Conjugate with a Fully Humanized Anti-MUC1 Antibody Shows Potent Antitumor Effects in Breast and Ovarian Tumor Xenografts by Hamann, Philip R, Hinman, Lois M, Beyer, Carl F, Lindh, Delores, Upeslacis, Janis, Shochat, Dan, Mountain, Andrew

    Published in Bioconjugate chemistry (01-03-2005)
    “…Murine CTM01 is an internalizing murine IgG1 monoclonal antibody that recognizes the MUC1 antigen expressed on many solid tumors of epithelial origin…”
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    Tumoricidal effect of calicheamicin immuno-conjugates using a passive targeting strategy by BOGHAERT, Erwin R, KHANDKE, Kiran, DISCAFANI, Carolyn, DAMLE, Nitin K, SRIDHARAN, Latha, ARMELLINO, Douglas, DOUGHER, Maureen, DIJOSEPH, John F, KUNZ, Arthur, HAMANN, Philip R, SRIDHARAN, Ashwin, JONES, Stanley

    Published in International journal of oncology (01-03-2006)
    “…Calicheamicin is a potent chemotherapeutic with a low therapeutic index that requires targeting to tumor cells for its use in the clinic. To treat acute…”
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    Preparation and characterization of monoclonal antibody conjugates of the calicheamicins : a novel and potent family of antitumor antibiotics by HINMAN, L. M, HAMANN, P. R, WALLACE, R, MENENDEZ, A. T, DURR, F. E, UPESLACIS, J

    Published in Cancer research (Chicago, Ill.) (15-07-1993)
    “…The calicheamicin family of antitumor antibiotics are capable of producing double-stranded DNA breaks at sub-picomolar concentrations. Their potency suggested…”
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    Synthesis and structure of the platelet aggregation factor thromboxane A2 by BHAGWAT, S. S, HAMANN, P. R, STILL, W. C, BUNTING, S, FITZPATRICK, F. A

    Published in Nature (London) (01-06-1985)
    “…In 1975, Hamberg et al. reported evidence for the existence of an unstable platelet-aggregating factor which they named thromboxane A2 (TXA2) and for which…”
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