YERVOY (ipilimumab) by Bristol Myers Squibb is ctla-4-directed antibody interactions [moa]. Approved for ctla-4-directed blocking antibody [epc]. First approved in 2011.
Drug data last refreshed 8h ago · AI intelligence enriched 1mo ago
YERVOY (ipilimumab) is a monoclonal antibody that blocks CTLA-4, a checkpoint inhibitor that unleashes anti-tumor immune responses. It is approved for melanoma and other solid tumors where it enhances T-cell activation against cancer cells. The drug pioneered checkpoint inhibitor immunotherapy and fundamentally changed oncology treatment paradigms.
LOE approaching signals team consolidation and transition focus toward combination therapies and new indications rather than monotherapy growth.
CTLA-4-directed Antibody Interactions
CTLA-4-directed Blocking Antibody
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
iSCIB1+ in Combination With Ipilimumab and Nivolumab as First-Line Treatment for Advanced Unresectable Melanoma
First-Line Ipilimumab Plus Nivolumab and Nogapendekin Alfa Inbakicept (N-803) in Patients With Stage IV or Recurrent Non-Small Cell Lung Cancer
A Randomized Trial of Fianlimab and Cemiplimab +/- Ipilimumab or Ipilimumab Plus Nivolumab in First-line Advanced Renal Cell Carcinoma (RCC)
TACE or Ablation Combined With Sintilimab and Ipilimumab N01 as Neoadjuvant Therapy for Resectable Hepatocellular Carcinoma With Intermediate-High Recurrence Risk
A Study to Evaluate the Safety and Tolerability of Pumitamig Alone or In Combination With Ipilimumab in Participants With First-Line Advanced or Unresectable Hepatocellular Carcinoma (HCC) (ROSETTA HCC-206)
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
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Upgrade to Pro — $25/moWorking on YERVOY during LOE approach positions you in a mature, high-impact cancer product with deep clinical evidence but declining growth trajectory. Roles emphasize defending market share, managing payer relationships, and supporting combination therapy strategies rather than growth driving.