Yervoy (ipilimumab) / BMS 
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 197 Diseases   398 Trials   398 Trials   21826 News 


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  • ||||||||||  CRS-207 / Novartis, Keytruda (pembrolizumab) / Merck (MSD), Yervoy (ipilimumab) / BMS
    Trial completion date, Trial primary completion date, Metastases:  Study of CRS-207, Pembrolizumab, Ipilimumab, and Tadalafil in Metastatic Pancreatic Cancer (clinicaltrials.gov) -  Mar 9, 2023   
    P2,  N=20, Recruiting, 
    Trial completion date: Dec 2023 --> Dec 2024 | Trial primary completion date: Dec 2023 --> Dec 2024
  • ||||||||||  Opdivo (nivolumab) / Ono Pharma, BMS, Yervoy (ipilimumab) / Ono Pharma, BMS
    Cost-Effectiveness of Nivolumab Plus Ipilimumab in Gastro-Oesophageal Cancer in Japan () -  Mar 9, 2023 - Abstract #ISPOR2023ISPOR_593;    
    Applying the threshold of JPY15 million/QALY, NIV+IPI treatment was not cost-effective. Further research on utility weights in the Japanese population and more valid biomarkers is needed for more refined analysis.
  • ||||||||||  Opdivo (nivolumab) / Ono Pharma, BMS, Yervoy (ipilimumab) / Ono Pharma, BMS
    Identifying and Quantifying Elements of Value for Nivolumab and Ipilimumab in First-Line Non-Small Cell Lung Cancer () -  Mar 9, 2023 - Abstract #ISPOR2023ISPOR_129;    
    We estimated the ROV attributable to the FDA accelerated approval (AA) pathway for checkpoint inhibitors (CPIs) following ipilimumab Including novel value elements in the cost-effectiveness analysis for N+I as first-line mNSCLC strategy was able to capture additional value beyond the traditional payer perspective.
  • ||||||||||  Keytruda (pembrolizumab) / Merck (MSD), Opdivo (nivolumab) / Ono Pharma, BMS, Yervoy (ipilimumab) / Ono Pharma, BMS
    Journal, Checkpoint inhibition, Mismatch repair, PD(L)-1 Biomarker, IO biomarker:  Expression of DNA mismatch repair proteins in melanoma patients treated with immune checkpoint inhibitors. (Pubmed Central) -  Mar 7, 2023   
    Reduced MMR protein expression is observed in CM and might predict favorable BOR in patients treated with ICI, as was observed for other entities. However, these findings need to be substantiated in larger patient cohorts.
  • ||||||||||  Opdivo (nivolumab) / BMS, Yervoy (ipilimumab) / BMS
    Trial primary completion date:  Study of Nivolumab and Ipilimumab in Children and Young Adults With INI1-Negative Cancers (clinicaltrials.gov) -  Mar 7, 2023   
    P2,  N=45, Recruiting, 
    New therapy strategies for irAE are currently tested, such as extracorporeal photopheresis, but larger prospective trials are lacking. Trial primary completion date: Oct 2023 --> Oct 2024
  • ||||||||||  Keytruda (pembrolizumab) / Merck (MSD), Yervoy (ipilimumab) / BMS
    Trial completion date, Trial primary completion date:  Pembrolizumab and Ipilimumab After Prior Immunotherapy for Melanoma (clinicaltrials.gov) -  Mar 6, 2023   
    P2,  N=70, Active, not recruiting, 
    Trial primary completion date: Oct 2023 --> Oct 2024 Trial completion date: Jun 2022 --> Jun 2026 | Trial primary completion date: Aug 2020 --> Jun 2022
  • ||||||||||  Jemperli (dostarlimab) / GSK, Opdivo (nivolumab) / Ono Pharma, BMS, Yervoy (ipilimumab) / Ono Pharma, BMS
    Journal, Checkpoint inhibition, Microsatellite instability, MSi-H Biomarker, PD(L)-1 Biomarker, IO biomarker:  Neoadjuvant Immune Checkpoint Inhibitor Therapy for Patients With Microsatellite Instability-High Colorectal Cancer: Shedding Light on the Future. (Pubmed Central) -  Mar 3, 2023   
    Although nonoperative management of patients with MMR-D/MSI-H rectal cancer with ICIs will potentially define our current therapeutic approach, therapeutic goals of neoadjuvant ICI therapy for patients with MMR-D/MSI-H colon cancer may differ given that nonoperative management has not been well established for colon cancer. Herein, we overview recent advancements in ICI-based therapies for patients with early-stage MMR-D/MSI-H colon and rectal cancer and elaborate on the future treatment paradigm of this unique subgroup of CRC.
  • ||||||||||  Keytruda (pembrolizumab) / Merck (MSD), Opdivo (nivolumab) / Ono Pharma, BMS, Yervoy (ipilimumab) / Ono Pharma, BMS
    Journal:  Neo-adjuvant immunotherapy emerges as best medical practice, and will be the new standard of care for macroscopic stage III melanoma. (Pubmed Central) -  Mar 2, 2023   
    Single agent anti-PD-1 achieves 20-30% MPR, the combination of ipilimumab and nivolumab doubles the MPR rates to 50-60%...S1801 compared TLND, followed by 18 courses of adjuvant pembrolizumab, to three courses of neoadjuvant pembrolizumab, followed by surgery and 15 adjuvant doses...There is rapid, consistent, and accumulating evidence generated from all phase 1 and phase 2 trials, indicating clinical superiority of neoadjuvant immunotherapy over adjuvant systemic therapy for macroscopic stage III melanoma. Therefore, payers should consider neoadjuvant immunotherapy for reimbursement
  • ||||||||||  Journal, Metastases:  Immunotherapy and Targeted Therapy for Advanced Gastroesophageal Cancer: ASCO Guideline. (Pubmed Central) -  Mar 2, 2023   
    For HER2-positive patients with gastric or GEJ AC who have progressed after first-line therapy, trastuzumab deruxtecan is recommended. In all cases, participation in a clinical trial is recommended as it is the panel's expectation that targeted treatment options for gastroesophageal cancer will continue to evolve.Additional information is available at www.asco.org/gastrointestinal-cancer-guidelines.
  • ||||||||||  Trial completion date, Trial primary completion date, Adverse events, Checkpoint inhibition:  Autoantibodies in Treatment With Immune Checkpoint Inhibitors (AUTENTIC) (clinicaltrials.gov) -  Mar 2, 2023   
    P=N/A,  N=221, Recruiting, 
    In all cases, participation in a clinical trial is recommended as it is the panel's expectation that targeted treatment options for gastroesophageal cancer will continue to evolve.Additional information is available at www.asco.org/gastrointestinal-cancer-guidelines. Trial completion date: Mar 2023 --> Dec 2023 | Trial primary completion date: Dec 2022 --> Oct 2023
  • ||||||||||  cisplatin/vinblastine/SHAO-FA (INT230-6) / Intensity Therap
    Trial completion, Trial completion date, Trial primary completion date, Metastases:  KEYNOTE-A10: A Phase 1/2 Safety Study of Intratumorally Dosed INT230-6 (clinicaltrials.gov) -  Mar 2, 2023   
    P1/2,  N=110, Completed, 
    Not yet recruiting --> Recruiting Active, not recruiting --> Completed | Trial completion date: Oct 2023 --> Feb 2023 | Trial primary completion date: Jul 2022 --> Feb 2023
  • ||||||||||  Opdivo (nivolumab) / Ono Pharma, BMS, Yervoy (ipilimumab) / Ono Pharma, BMS
    Biomarker, Journal, PD(L)-1 Biomarker, FDG PET, Metastases:  FDG PET/CT Prognostic Markers in Patients with Advanced Melanoma Treated with Ipilimumab and Nivolumab. (Pubmed Central) -  Mar 1, 2023   
    Active, not recruiting --> Completed | Trial completion date: Oct 2023 --> Feb 2023 | Trial primary completion date: Jul 2022 --> Feb 2023 Conclusion Baseline fluorine 18 fluorodeoxyglucose PET/CT metabolic tumor volume was an independent prognostic marker in patients with advanced melanoma who received ipilimumab and nivolumab treatment.
  • ||||||||||  Skyrizi (risankizumab) / AbbVie, Boehringer Ingelheim, Keytruda (pembrolizumab) / Merck (MSD)
    Journal, PD(L)-1 Biomarker, IO biomarker, Metastases:  Pembrolizumab-induced plaque psoriasis successfully treated with risankizumab in a patient with stage IV cutaneous melanoma. (Pubmed Central) -  Feb 27, 2023   
    Immune checkpoint inhibitors, such as pembrolizumab and nivolumab, are monoclonal antibodies that block programmed cell death 1 (PD-1) expressed on activated CD8+ T cells and play a crucial role in the treatment of advanced melanoma...After the surgery and the failure of ipilimumab and IL-2, he started immunotherapy with pembrolizumab...Our patient's rapid response to risankizumab enabled us to continue immunotherapy with pembrolizumab. The recognition of cutaneous signs of toxicity related to such drugs for advanced melanoma is of primary importance to start the correct treatment and continue the immunotherapy when possible.