Abstract:
The present invention relates to a pharmaceutical composition for combination therapy for preventing and/or treating cancer comprising a c-Met inhibitor and a beta-catenin inhibitor as active ingredients, to use of c-Met inhibitor efficacy enhancement by the beta-catenin inhibitor, and use of beta-catenin inhibitor efficacy enhancement by the c-Met inhibitor. The combination therapy of the c-Met inhibitor and beta-catenin inhibitor enables treatment of diseases which could not be treated by the c-Met inhibitor alone, thereby extending indications and overcoming resistance against the c-Met inhibitor.
Abstract:
The present invention relates to a pharmaceutical composition for coadministration to prevent and treat angiogenesis-related diseases containing an anti-c-Met antibody and an anti-Ang2 antibody. By coadministration of the anti-c-Met antibody and the anti-Ang2 antibody provided in the present invention, improved treatment is possible though effects of inhibiting growth of cancer cells and angiogenesis. Accordingly, excellent synergy treatment effect can be expected in various angiogenesis diseases which can′t obtain treatment effect or show little effect only for administration of an existing antibody.
Abstract:
Provided is a pharmaceutical composition containing anti-c-Met antibody and sorafenib as active ingredients for a combination therapy for preventing and/or treating cancer diseases. The pharmaceutical composition for a combination therapy has an excellent synergistic effect and can reduce the effective dose of the anti-c-Met antibody, thereby can more effectively treat the cancer.
Abstract:
Provided is a pharmaceutical composition containing anti-c-Met antibody and FGFR inhibitor as active ingredients for a combination therapy for preventing and/or treating cancer diseases. The pharmaceutical composition for a combination therapy has an excellent synergistic effect and can reduce the effective dose of the anti-c-Met antibody, thereby can more effectively treat the cancer.
Abstract:
The present invention provides: a composition for testing effects of a c-Met antibody including a gene marker; and a method for testing effects of a c-Met antibody using the same gene marker. The composition includes one or more selected from a group consisting of a TNFRSF21 (Tumor necrosis factor receptor superfamily, member 21) gene, a CASP10 (Caspase 10) gene, a TP53 (Tumor protein p53) gene, a BCL2 (B-cell CLL/lymphoma 2) gene, a BCL2L1 (BCL2-like 1) gene, and protein encoded by the same genes. According to the present invention, an antibody with high efficacy can be quickly screened.
Abstract:
Provided is a pharmaceutical composition for a combination therapy containing a p53 activator and a c-Met inhibitor as an active component. The pharmaceutical composition for the combination therapy expresses excellent synergistic effects and reduces an effective does of the p53 activator and the c-Met inhibitor, thereby enabling efficient treatment.
Abstract:
Provided is a pharmaceutical composition for a combination therapy which contains an angiogenesis inhibitor and an anti-c-Met antibody or an antigen-binding fragment thereof as an active ingredient for preventing and/or treating c-Met and angiogenic factor induced diseases. The pharmaceutical composition for the combination therapy has a superior synergistic effect, thereby more effective treatments are available.
Abstract:
PURPOSE: An anti-c-Met humanized antibody and use thereof are provided to efficiently prevent and treat cancer. CONSTITUTION: Anti-c-Met humanized antibody comprises a medium variable region consisting of amino acid sequence of sequence number 1 and a light variable region consisting of amino acid sequence of sequence number 2. The light variable region comprises a medium variable domain comprised of amino acid sequence of sequence number 3 and amino acid sequence of sequence number 4.