Erbitux (cetuximab) / Eli Lilly 
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  • ||||||||||  Clinical, Journal:  Efficacy of second-line chemotherapy after a first-line triplet in patients with metastatic colorectal cancer. (Pubmed Central) -  Feb 24, 2020   
    Exposing patients with metastatic colorectal cancer (mcrc) to all three active chemotherapeutic agents (oxaliplatin, irinotecan, fluorouracil) has improved survival...Concurrent bevacizumab was given in 16 patients (57%), and cetuximab, in 2 (7%)...Median progression-free survival was 4.8 months (95% ci: 2.4 months to 9.6 months), and overall survival was 15 months (95% ci: 9.6 months to 20.4 months). Second-line chemotherapy after first-line triplet therapy in mcrc is feasible and suggests efficacy comparable to that reported for second-line therapy after a doublet, regardless of the agent used.
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono
    Trial completion date, Metastases:  CA225200: PhII ICb With/Without Erbitux in MBC Pts (clinicaltrials.gov) -  Feb 23, 2020   
    P2,  N=154, Active, not recruiting, 
    Trial completion date: Jun 2023 --> Jun 2024 | Trial primary completion date: Dec 2022 --> Dec 2023 Trial completion date: Dec 2019 --> Dec 2020
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono
    Journal:  Non-invasive targeted iontophoretic delivery of cetuximab to skin. (Pubmed Central) -  Feb 21, 2020   
    Therapeutic concentrations of CTX in the viable epidermis, upper dermis and lower dermis were achieved following iontophoresis for 2, 4 and 8 h, respectively. The results demonstrate the topical delivery of a 152 kDa monoclonal antibody into skin in a targeted, controlled and entirely non-invasive manner.
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono, doxorubicin hydrochloride / Generic mfg.
    Journal:  Selective delivery of doxorubicin to EGFR+ cancer cells by Cetuximab-DNA conjugates. (Pubmed Central) -  Feb 20, 2020   
    In vitro cytotoxicity and selectively cancer cell killing was investigated against two EGFR+ cell lines (KB and MDA-MB-231) and one EGFR- cell line (NIH-3T3). Cytotoxicity and flow cytometer data showed that doxorubicin loaded in cetuximab-DNA conjugates were more potent in cell cytotoxicity than free doxorubicin in EGFR overexpressed cell lines, suggesting that they were more selectively and easily taken up within cells followed by rapid release of doxorubicin from the system into the cytoplasm from endosomes.
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono
    Journal:  Osteopontin Mediates Cetuximab Resistance via the MAPK Pathway in NSCLC Cells. (Pubmed Central) -  Feb 19, 2020   
    These results suggested that OPN promoted malignant progression and mediated drug resistance via the MAPK signaling pathway in NSCLC cells. This study reveals the important role of OPN in NSCLC cells, making it a potential target for improving chemotherapy efficiency in patients with NSCLC.
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono
    Journal:  EGFR-Specific Tyrosine Kinase Inhibitor Modifies NK Cell-Mediated Antitumoral Activity against Ovarian Cancer Cells. (Pubmed Central) -  Feb 15, 2020   
    We studied treatment-related structural and functional changes on tumor and immune cells in the presence of the anti-EGFR antibody cetuximab and investigated NK-mediated antitumoral activity...Our data suggest that sensitization of tumor cells by anti-EGFR TKIs differentially modulates interactions with NK cells. These data have important implications for the design of chemo-immuno combination therapies in this tumor entity.
  • ||||||||||  Clinical, Review, Journal:  Adjuvant chemotherapy in resected colon cancer: When, how and how long? (Pubmed Central) -  Feb 14, 2020   
    Only oxaliplatin added to fluorouracil/capecitabine has been shown to be superior beyond a fluropyrimidine alone in the adjuvant setting...In the era of cancer gene expression-based subtyping, the Colorectal Cancer Subtyping Consortium has proposed a four-subgroup molecular classification system for colorectal cancer, consisting of CMS1 (immune), CMS2 (canonical), CMS3 (metabolic) and CMS4 (mesenchymal). In this review, we present and analyze the available data on efficacy and toxicity of the combination regimen approved for treatment of resected colon cancer, and discuss the questions of when, how and how long we need to treat such patients.
  • ||||||||||  cisplatin / Generic mfg., Erbitux (cetuximab) / Eli Lilly, EMD Serono
    Clinical, Review, Journal:  Treating Patients With Locally Advanced Squamous Cell Carcinoma of the Head and Neck Unsuitable to Receive Cisplatin-Based Therapy. (Pubmed Central) -  Feb 13, 2020   
    Patients with any pre-existing comorbidities that may be exacerbated by high-dose cisplatin treatment can be redirected to a non-cisplatin-based option to minimize the risk of treatment non-adherence. High-dose cisplatin plus radiotherapy remains the preferred treatment for fit patients with unresected LA SCCHN; patients who are unsuitable or borderline unsuitable for high-dose cisplatin could be identified using available tests for potential comorbidities and should be offered alternative treatments, such as cetuximab plus radiotherapy.
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono
    Nanoparticle encapsulated TLR7/8 agonists activate both innate and adaptive immune responses (204B, Pennsylvania Convention Center) -  Feb 13, 2020 - Abstract #ACSSp2020ACS_Sp_10555;    
    TLR7/8 agonist-loaded NP treatment significantly enhanced the anti-tumor efficacy of cetuximab and an anti-HER2/neu antibody in mouse tumor models. Our results suggest that acidic-pH responsive polymeric nanoparticles are an efficient TLR7/8 agonist delivery platform for cancer immunotherapy.
  • ||||||||||  Orencia (abatacept) / BMS, Erbitux (cetuximab) / Eli Lilly, EMD Serono
    Fast dynamic surfactant reduces aggregation of biologics (Freedom Ballroom E/F, Philadelphia 201 Hotel) -  Feb 13, 2020 - Abstract #ACSSp2020ACS_Sp_7983;    
    FM1000 also reduced subvisible particle formation in a cetuximab model formulation. Coupling aggregation performance with fundamental surfactant interfacial dynamics and behavior will help better understand the underlying mechanisms of protein (de)stabilization, enabling the development of higher stability formulations.