Abstract:
Provided herein are conditionally-active anti-EGFR antibodies, antigen- binding fragments thereof and conjugates thereof, including antibody-drug conjugates (ADCs), containing conditionally active anti-EGFR antibodies, a linker and a targeted agent for delivery. Also provided are methods of treatment and uses of the conditionally-active anti-EGFR antibody, antigen-binding fragments thereof and conjugates thereof, including antibody-drug conjugates (ADCs).
Abstract:
The present disclosure provides compositions and methods for treatment of bladder cancer. The methods include administering an immunoconjugate having a binding protein that specifically binds to Ep-CAM and a toxin to a subject in need of treatment for bladder cancer. In one aspect, the present disclosure provides methods for treating bladder cancer in a subject in need thereof, wherein the methods comprise administering to the subject an immunoconjugate, and wherein the administration is sufficient to result in event-free survival of the subject. In some embodiment's, the administration is sufficient to result in event-free survival of the subject for at least 12 months following the first dose of the the immunoconjugate. In some embodiment's, the administration is sufficient to result in event free survival of the subject for at least about 18 months following the first dose of the immunoconjugate.
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 the cancers listed in Table I. Consequently, the ADC's of the invention provide a therapeutic composition for the treatment of cancer.
Abstract:
The invention described herein is related to antibodies directed to the antigen TIM-1 and uses of such antibodies for the treatment of cancer (e.g., renal and ovarian cancer). In particular, there are provided fully human monoclonal antibodies directed to the antigen TIM-1. Isolated polynucleotide sequences encoding, and amino acid sequences comprising, heavy and light chain immunoglobulin molecules, particularly sequences corresponding to contiguous heavy and light chain sequences spanning the framework regions (FR' s) and/or complementarity determining regions (CDR' s), specifically from FRl through FR4 or CDRl through CDR3, are provided. Hybridomas or other cell lines expressing such immunoglobulin molecules and monoclonal antibodies are also provided.
Abstract:
Antibodies and molecules derived therefrom that bind to novel STEAP-1 protein, and variants thereof, are described wherein STEAP-1 exhibits tissue specific expression in normal adult tissue, and is aberrantly expressed in the cancers listed in Table I. Consequently, STEAP-1 provides a diagnostic, prognostic, prophylactic and/or therapeutic target for cancer. The STEAP-1 gene or fragment thereof, or its encoded protein, or variants thereof, or a fragment thereof, can be used to elicit a humoral or cellular immune response; antibodies or T cells reactive with STEAP-1 can be used in active or passive immunization.
Abstract:
The invention concerns the techniques related to the insertion of foreign nucleic acid in cells. More particularly it concerns a DNA/antibody conjugate enabling an efficient foreign DNA expression in vivo or in vitro in protein form in target cells.
Abstract:
Tubulysin compounds of the formula (I) where R 1 , R 2 R 3a , R 3b , R 4 , R 5 , W, and n are as defined herein, are anti-mitotic agents that can be used in the treatment of cancer, especially when conjugated to a targeting moiety.
Abstract:
Antibody drug conjugates (ADC's) that bind to 191P4D12 protein and variants thereof are described herein. 191P4D12 exhibits tissue specific expression in normal adult tissue, and is aberrantly expressed in the cancers listed in Table I. Consequently, the ADC's of the invention provide a therapeutic composition for the treatment of cancer.