Erbitux (cetuximab) / Eli Lilly 
Welcome,         Profile    Billing    Logout  
 245 Diseases   389 Trials   389 Trials   11400 News 


«12345678910111213...143144»
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono, Vectibix (panitumumab) / Amgen
    Real-world use of anti-EGFR therapy in metastatic colorectal cancer. (Hall A; Poster Bd #: 215) -  Apr 24, 2024 - Abstract #ASCO2024ASCO_2621;    
    Based on results from the Flatiron Health database, use of anti-EGFR therapy is enriched among patients with biomarker-based indications for treatment. Notably, anti-EGFR therapy was employed in only 56.6% of patients with RAS and RAF wildtype, left-sided mCRC, with decreased use observed from 2013 to 2023.
  • ||||||||||  Avastin (bevacizumab) / Roche, Erbitux (cetuximab) / Eli Lilly, EMD Serono
    Journal:  Augmenting external control arms using Bayesian borrowing: a case study in first-line non-small (Pubmed Central) -  Apr 23, 2024   
    In this secondary analysis of a clinical trial, more contact days early in the course was associated with declines in physical function and worse survival in all-comers and in participants receiving cancer-directed treatment. Materials & An ECA for a randomized controlled trial (RCT) in first-line NSCLC was constructed using ConcertAI Patient360
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono
    Review, Journal:  Cetuximab chemotherapy resistance: Insight into the homeostatic evolution of head and neck cancer (Review). (Pubmed Central) -  Apr 23, 2024   
    The few resistant cells that survive in this new environment obtain differential reproductive success that enables them to pass down the newly selected resistant gene pool. The present review aims to summarize key findings of tumor evolution, epithelial?mesenchymal transition and resistance to cetuximab therapy in head and neck squamous cell carcinoma.
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono
    Enrollment open:  LIGHTNING: Real-time Margin Assessment in Head and Neck Cancer (clinicaltrials.gov) -  Apr 22, 2024   
    P2,  N=20, Recruiting, 
    The present review aims to summarize key findings of tumor evolution, epithelial?mesenchymal transition and resistance to cetuximab therapy in head and neck squamous cell carcinoma. Not yet recruiting --> Recruiting
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono
    Journal:  Biodistribution and therapeutic efficacy of a gold nanoparticle-based targeted drug delivery system against pancreatic cancer. (Pubmed Central) -  Apr 22, 2024   
    Among the various formulations tested, 5?nm gold nanoparticles coated with gemcitabine, cetuximab and poly-ethylene glycol (PEG) of molecular weight 1000?Da, which we named ACGP441000, demonstrated optimal efficacy in inhibiting tumor growth. The current study reveals an opportunity to target PCCs and PSCs simultaneously, by exploiting their overexpression of EGFR as a target, in order to inhibit pancreatic cancer growth.
  • ||||||||||  Review, Journal, PD(L)-1 Biomarker, IO biomarker:  Therapeutic Advances and Challenges for the Management of HPV-Associated Oropharyngeal Cancer. (Pubmed Central) -  Apr 17, 2024   
    The most common drugs to treat HPV-associated OPC under these clinical trials and implemented as well for HPV-negative HNC include cisplatin, nivolumab, cetuximab, paclitaxel, pembrolizumab, 5-fluorouracil, and docetaxel...In this context, we identified most mutated genes found in HPV-associated OPC that can represent potential targets for drug development. These include TP53, PIK3CA, PTEN, NOTCH1, RB1, FAT1, FBXW7, HRAS, KRAS, and CDKN2A.
  • ||||||||||  MK-1084 / Merck (MSD), Otsuka
    Enrollment change, Combination therapy, Monotherapy, Metastases:  A Study of MK-1084 in KRAS Mutant Advanced Solid Tumors (MK-1084-001) (clinicaltrials.gov) -  Apr 17, 2024   
    P1,  N=830, Recruiting, 
    These include TP53, PIK3CA, PTEN, NOTCH1, RB1, FAT1, FBXW7, HRAS, KRAS, and CDKN2A. N=450 --> 830
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono
    Journal:  Antibody-platinum (IV) prodrugs conjugates for targeted treatment of cutaneous squamous cell carcinoma. (Pubmed Central) -  Apr 15, 2024   
    Cisplatin (CisPt) shows good curative effects; however, its adverse effects and non-tumor-targeting ability are major drawbacks...Specifically, it accurately delivered C8Pt(IV) into tumor cells to exert the combined anti-tumor effect of Cet and CisPt. Herein, metabolomic analysis showed that Cet-C8Pt(IV) promoted cellular apoptosis and increased DNA damage in cSCC cells by affecting the vitamin B6 metabolic pathway in tumor cells, thereby further enhancing the tumor-killing ability and providing a new strategy for clinical cancer treatment using antibody-platinum (IV) prodrugs conjugates.
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono
    Journal, Cancer stem:  Inhibition of the AURKA/YAP1 axis is a promising therapeutic option for overcoming cetuximab resistance in colorectal cancer stem cells. (Pubmed Central) -  Apr 15, 2024   
    Herein, metabolomic analysis showed that Cet-C8Pt(IV) promoted cellular apoptosis and increased DNA damage in cSCC cells by affecting the vitamin B6 metabolic pathway in tumor cells, thereby further enhancing the tumor-killing ability and providing a new strategy for clinical cancer treatment using antibody-platinum (IV) prodrugs conjugates. AURKA inhibition holds promise as a therapeutic approach to overcome cetuximab resistance in RAS/RAF wild-type colorectal cancer, offering a potential means to counter the development of cancer stem cell phenotypes associated with cetuximab resistance.
  • ||||||||||  Krazati (adagrasib) / BMS
    Trial completion date, Trial primary completion date, Metastases:  Phase 1/2 Study of MRTX849 in Patients With Cancer Having a KRAS G12C Mutation KRYSTAL-1 (clinicaltrials.gov) -  Apr 11, 2024   
    P1/2,  N=822, Recruiting, 
    Our findings indicate that anti-EGFR antibodies bound to N-BPs can improve the antitumor effects of the native antibody possibly increasing the therapeutic effect. Trial completion date: Sep 2024 --> Jan 2026 | Trial primary completion date: Dec 2023 --> Jul 2025
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly
    Trial completion date, Trial primary completion date:  Cetuximab After Immunotherapy for the Treatment of Head and Neck Squamous Cell Cancer (clinicaltrials.gov) -  Apr 8, 2024   
    P2,  N=30, Recruiting, 
    Situations of genetic mutations were differentiated from first-line PD to second-line PD, which indicated that mutation detection may contribute to predict prognosis of mCRC patients. Trial completion date: Aug 2024 --> Jan 2025 | Trial primary completion date: Mar 2024 --> Sep 2024
  • ||||||||||  Krazati (adagrasib) / BMS, Erbitux (cetuximab) / Eli Lilly, EMD Serono
    Journal, Metastases:  Efficacy and Safety of Adagrasib plus Cetuximab in Patients with KRASG12C-Mutated Metastatic Colorectal Cancer. (Pubmed Central) -  Apr 8, 2024   
    Adagrasib plus cetuximab demonstrates promising clinical activity and tolerable safety in heavily pretreated patients with unresectable or metastatic KRASG12C-mutated colorectal cancer. These data support a potential new standard of care and highlight the significance of testing and identification of KRASG12C mutations in patients with colorectal cancer.
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono, Vectibix (panitumumab) / Amgen
    Review, Journal, Metastases:  Current advances in targeted therapy for metastatic colorectal cancer - Clinical translation and future directions. (Pubmed Central) -  Apr 8, 2024   
    The non-invasive monitoring of molecular resistance to targeted therapies using Next Generation Sequencing analysis of circulating tumor-derived DNA (ctDNA) and captured sequencing of tumors have improved patient selection for targeted therapies. This review will focus on how latest advances, challenges and future directions in the development of targeted therapies in mCRC.
  • ||||||||||  PF-07284892 / Pfizer
    Enrollment change, Combination therapy, Metastases:  PF-07284892 in Participants With Advanced Solid Tumors (clinicaltrials.gov) -  Apr 4, 2024   
    P1,  N=53, Active, not recruiting, 
    Trial completion date: Apr 2027 --> Nov 2026 | Trial primary completion date: Apr 2027 --> Nov 2026 N=36 --> 53
  • ||||||||||  fosifloxuridine nafalbenamide (NUC-3373) / NuCana
    Trial completion, Enrollment change, Trial completion date, Trial primary completion date, Combination therapy:  NuTide:302: A Safety, Pharmacokinetic and Efficacy Study of NUC-3373 in Combination With Standard Agents Used in Colorectal Cancer Treatment (clinicaltrials.gov) -  Apr 3, 2024   
    P1/2,  N=107, Completed, 
    Phase classification: P1 --> P1/2 | N=168 --> 352 | Trial completion date: May 2025 --> Sep 2026 | Trial primary completion date: May 2025 --> Sep 2026 Recruiting --> Completed | N=225 --> 107 | Trial completion date: Nov 2023 --> Mar 2024 | Trial primary completion date: Nov 2023 --> Mar 2024
  • ||||||||||  Review, Journal:  Targeting KRAS G12C Mutation in Colorectal Cancer, A Review: New Arrows in the Quiver. (Pubmed Central) -  Apr 1, 2024   
    Other combinations such as adagrasib-cetuximab, divarasib-cetuximab, or FOLFIRI-panitumumab-sotorasib have also shown a meaningful response rate and are currently under evaluation...In this setting, liquid biopsy emerges as a critical tool to characterize the mechanisms of resistance, consisting mainly of acquired genomic alterations in the MAPK and PI3K pathways and tyrosine kinase receptor alterations, but gene fusions, histological changes, or conformational changes in the kinase have also been described. In this paper, we review the development of KRAS G12C inhibitors in colorectal cancer as well as the main mechanisms of resistance.