Erbitux (cetuximab) / Eli Lilly 
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  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono, magrolimab (GS-4721) / Ono Pharma, Gilead
    Leveraging CRISPR-Cas9 screening platform for discovery of novel tumor intrinsic phagocytosis modulators (Hall C) -  Oct 6, 2022 - Abstract #SITC2022SITC_1752;    
    Conclusions We successfully established and implemented multiple macrophage and tumor cell co-culture screening platforms, and systematically revealed tumor intrinsic regulators of phagocytosis, uncovering multiple known and novel therapeutic targets regulating vulnerability of tumor cells to macrophage-mediated phagocytosis. Our proprietary high-throughput phagocytosis CRISPR screening platform provides an unbiased and rapid solution to study macrophage and tumor cell interactions and discover novel targets for cancer therapy.
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono, Herceptin (trastuzumab) / Roche, Rituxan (rituximab) / Biogen, Zenyaku Kogyo, Roche
    Antibody-lectin bispecifics for glyco-immune checkpoint blockade (Hall C) -  Oct 6, 2022 - Abstract #SITC2022SITC_1517;    
    Conclusions These studies provide proof-of-principle for AbLecs as a first-in-class, modular platform technology enabling blockade of glyco-immune checkpoints for cancer immunotherapy. Download figure Open in new tab Download powerpoint Abstract 1209 Figure 1 Graphical abstract
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono, Rituxan (rituximab) / Biogen, Zenyaku Kogyo, Roche, ES004 / Elpiscience
    Treatment of anti-SIRPα in combination with anti-TAA exerts superior anti-tumor activity (Hall C) -  Oct 6, 2022 - Abstract #SITC2022SITC_1107;    
    Conclusions In summary, the functional anti-SIRPα mAb ES004-B5 has great potential to be used in combinations with multiple anti-TAA antibodies in cancer treatment. We are currently advancing the development of ES004-B5 into clinical candidate.
  • ||||||||||  FT538 / Fate Therap
    Interim Phase I clinical data of FT538, an off-the-shelf, multiplexed-engineered, iPSC-derived NK cell therapy, combined with monoclonal antibodies in patients with advanced solid tumors (Hall C) -  Oct 6, 2022 - Abstract #SITC2022SITC_1045;    
    P1
    Treatment consists of two, 29-day treatment cycles, each consisting of 3 days outpatient conditioning chemotherapy (cyclophosphamide 500 mg/m 2 and fludarabine 30 mg/m 2 ), followed by 3 outpatient once-weekly doses of FT538; mAbs are administered at standard dose and schedule...Dose escalation is based on a modified toxicity probability interval algorithm dose-escalation design with a starting dose level of 100 million FT538 cells/dose in combination with avelumab or pembrolizumab in PD-L1-expressing solid tumors; trastuzumab in HER2-expressing tumors; or cetuximab in colorectal cancer, squamous head and neck or lung cancers, or epidermal growth factor receptor-mutated lung cancer...Dose escalation is ongoing. Conclusions Interim clinical data, including safety and tolerability and initial anti-tumor activity, from the ongoing Phase I dose-escalation study of FT538 combined with anti-PD-1/L1 or ADCC-competent mAbs in advanced solid tumors will be presented at the conference.
  • ||||||||||  CDX-1140 / Celldex, Keytruda (pembrolizumab) / Merck (MSD)
    Results from a Phase 1 study of CDX-1140, a fully human anti-CD40 agonist monoclonal antibody (mAb), in combination with pembrolizumab (Hall C) -  Oct 6, 2022 - Abstract #SITC2022SITC_923;    
    P1
    Further studies are warranted. Trial Registration NCT03329950 Ethics Approval The study was reviewed and approved by the following institutional review boards: Providence Health & Services Institutional Review Board for Earle A. Chiles Research Institute/Providence Cancer Institute; approval number/ID: PHS IRB #2017000532 WCG-IRB for Gabrail Cancer Center, Georgia Cancer Specialists, HonorHealth Research Institute, and Nebraska Cancer Specialists; approval number/ID: 20172645 Rhode Island Hospital IkRB#1 for Legorreta Cancer Center at Brown University/Rhode Island Hospital/Lifespan Cancer Center; approval number/ID: LS-P-Camp Office of Regulatory Affairs of the University of Pennsylvania for Hospital of the University of Pennsylvania; approval number/ID: UPCC 18917 Memorial Sloan Kettering Cancer Center Institutional Review Board/Privacy Board; approval number/ID: 18-225 Participants gave informed consent before taking part in the study.
  • ||||||||||  AB-101 / Artiva Biotherap
    Evaluation of AB-101, an Allogeneic Cord Blood-derived Natural Killer (NK) Cell Therapy, as an ADCC Enhancer in Hematologic and Solid Tumors (Hall C) -  Oct 6, 2022 - Abstract #SITC2022SITC_643;    
    P1/2
    In addition, in vivo efficacy of AB-101 and AB-101 in combination with rituximab demonstrated enhanced median survival in the Raji xenograft model and AB-101 in combination with trastuzumab led to enhanced survival in the SKOV-3 xenograft model...AB-101 is currently in a Ph1 clinical trial to evaluate the safety and anti-tumor activity alone and in combination with rituximab in patients with relapsed or refractory NHL (ClinicalTrials.gov: NCT04673617 ). Ethics Approval All animal work was conducted under reviewed IACUC protocol and with approval of an IACUC committee at each center where the studies took place.
  • ||||||||||  Bavencio (avelumab) / EMD Serono, Pfizer, Erbitux (cetuximab) / Eli Lilly, EMD Serono, Herceptin (trastuzumab) / Roche
    iPSC-derived NK cells engineered with a novel TGFβ signal redirector receptor exhibit enhanced performance against solid tumors (Hall C) -  Oct 6, 2022 - Abstract #SITC2022SITC_596;    
    Conclusions Collectively, the data illustrate that a customized TGFβ-SRR construct can redirect TGFβ-mediated suppression and potentiate effector cell function to enhance the anti-tumor activity of iNK cells. This novel synthetic receptor represents an innovative strategy to enable adoptively-transferred cell therapy to overcome the immunosuppressive TME for the successful treatment of bulky tumors.
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono
    Enrollment closed:  RTOG-1016: Radiation Therapy With Cisplatin or Cetuximab in Treating Patients With Oropharyngeal Cancer (clinicaltrials.gov) -  Oct 5, 2022   
    P3,  N=987, Active, not recruiting, 
    This probe showed better imaging resolution and higher sensitivity in detecting subtle metastases derived from an orthotopic ESCC model than NIR-I, which indicates that NIR-II has promise in guiding precise surgery for ESCC patients. Unknown status --> Active, not recruiting
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono, avutometinib (VS-6766) / Verastem
    Enrollment open, Trial initiation date, Metastases:  A Study of VS-6766 and Cetuximab in Patients With Advanced Colorectal Cancer (clinicaltrials.gov) -  Oct 4, 2022   
    P1b/2,  N=53, Recruiting, 
    Trial completion date: Sep 2022 --> Sep 2023 | Trial primary completion date: Sep 2022 --> Sep 2023 Not yet recruiting --> Recruiting | Initiation date: Apr 2022 --> Aug 2022
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono
    Drastic response to cetuximab in metastatic eccrine porocarcinoma with EGFR amplification (Summit 2) -  Oct 1, 2022 - Abstract #ESMOAsia2022ESMO_Asia_399;    
    As an initial chemotherapy, carboplatin and docetaxel were administered every 3 weeks...Based on this result, cetuximab (400 mg/m 2 once, then 250 mg/m 2 per week) in association with 5-FU/LV (200 mg/m 2 leucovorin, 400 mg/m 2 bolus fluorouracil, and 2400 mg/m 2 infusional fluorouracil per 2 weeks) were administered...Table 1. Comprehensive genomic profiling by FoundationOne ®CDx
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono
    Multi-omics signature for identification of RAS wild-type colorectal cancer liver metastases sensitive to anti-EGFR therapy (Summit 2) -  Oct 1, 2022 - Abstract #ESMOAsia2022ESMO_Asia_336;    
    P4
    In this study, we aimed to develop and validate a multi-omics deep learning model to predict cetuximab efficacy in RAS wild type mCRC patients...Conclusions The multi-omic signature can serve as an intermediate surrogate marker of anti-EGFR treatment sensitivity and survival. The signature outperformed known biomarkers in providing an early prediction of treatment sensitivity and could be used to Ras wild type mCRC treatment decisions.
  • ||||||||||  fulzerasib (GFH925) / GenFleet Therap
    Enrollment open, Trial primary completion date, Combination therapy, Metastases:  A Study of IBI351 in Combination With Cetuximab in Subjects With KRAS G12C Mutated Metastatic Colorectal Cancer (clinicaltrials.gov) -  Sep 30, 2022   
    P1,  N=80, Recruiting, 
    Our data suggest that vorinostat is a potentially effective radiosensitizer for use during the treatment of peritoneal dissemination of gastric cancer by ipRIT with Cu-cetuximab. Not yet recruiting --> Recruiting | Trial primary completion date: Aug 2022 --> Aug 2023
  • ||||||||||  Review, Journal:  Studying molecular signaling in major angiogenic diseases. (Pubmed Central) -  Sep 29, 2022   
    In clinical therapeutics, target therapy focusing on discovery of novel anti-angiogenic agents like bevacizumab, cetuximab, sunitinib, imatinib, lenvatinib, thalidomide, everolimus etc., to block or inhibit the angiogenesis pathway is well explored in recent times. In this review, we will discuss about the molecular signaling pathways involved in major angiogenic diseases in detail.
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono
    Journal:  c-Met Signaling as a Therapeutic Target in Head and Neck Cancer. (Pubmed Central) -  Sep 29, 2022   
    Inhibition of the c-Met pathway may subvert oncogenesis within the tumor-intrinsic compartment, blocking tumoral proliferation, invasion, migration, and metastasis, or the tumor-extrinsic compartment, modulating the immunosuppressive tumor microenvironment. This review discusses the rationale and current drug development strategies for targeting c-Met or its exclusive ligand hepatocyte growth factor (HGF) in HNSCC.
  • ||||||||||  Ibrance (palbociclib) / Pfizer, Erbitux (cetuximab) / Eli Lilly, EMD Serono
    Journal:  The Potential for Selective Cyclin-Dependent Kinase 4/6 Inhibition in the Therapy for Head and Neck Squamous Cell Carcinoma. (Pubmed Central) -  Sep 29, 2022   
    However, correlative biomarker analyses identified that trends for better overall survival with palbociclib and cetuximab were observed in certain prespecified subsets; the largest reduction in risk of death with palbociclib versus placebo and cetuximab occurred in the subset with CDKN2A mutations. Several phase II-III trials are underway investigating palbociclib in biomarker-selected patients with HPV-unrelated locally advanced or recurrent or metastatic HNSCC.
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono, Vectibix (panitumumab) / Amgen, Takeda
    Review, Journal:  Promotion or remission: a role of noncoding RNAs in colorectal cancer resistance to anti-EGFR therapy. (Pubmed Central) -  Sep 29, 2022   
    In addition, some ncRNAs that are involved in the regulation of signaling pathways or genes related to anti-EGFR resistance, but need to be further verified by resistance experiments were also included in this review, thereby providing more ideas and basis for ncRNAs as CRC prognostic markers and anti-EGFR therapy sensitizers. Video Abstract.