

What is Yervoy (ipilimumab)? Learn about its uses, FDA-approved indications, dosage, how it's given, and what patients need to know in 2026.
Yervoy is the brand name for ipilimumab, a prescription immunotherapy drug made by Bristol Myers Squibb. It belongs to a class of medications called immune checkpoint inhibitors. Specifically, Yervoy targets a protein called CTLA-4, which normally acts as a brake on your immune system.
By blocking CTLA-4, Yervoy releases that brake and allows your immune system's T-cells to become more active against cancer cells. It was one of the first checkpoint inhibitors approved by the FDA and represented a major breakthrough in cancer treatment.
For a deeper dive into the science, see our guide on how Yervoy works.
Yervoy is FDA-approved for several types of cancer, either as a standalone treatment or in combination with nivolumab (Opdivo), another checkpoint inhibitor. Here are its approved uses:
Yervoy is administered as an intravenous (IV) infusion. You cannot take it as a pill or inject it at home. Here's what to expect:
The dose of Yervoy depends on which cancer is being treated and whether it's used alone or with nivolumab:
Your oncologist will determine the right dose based on your weight, the type of cancer, and your overall health. Doses may be delayed or discontinued if you develop significant side effects.
Because Yervoy activates the immune system, it can cause immune-mediated side effects — situations where your immune system attacks healthy tissue. Common side effects include fatigue, diarrhea, itching, rash, and nausea.
Serious side effects include immune-mediated colitis, hepatitis, skin reactions, endocrine disorders, pneumonitis, nephritis, and myocarditis. Yervoy carries a boxed warning about these risks.
Read our detailed guide on Yervoy side effects to learn what to watch for and when to seek help.
Yervoy is one of the more expensive cancer treatments available:
Most patients don't pay this out of pocket. Yervoy is typically covered by Medicare Part B and commercial insurance as a physician-administered drug. Prior authorization is usually required.
Bristol Myers Squibb offers a co-pay assistance program for commercially insured patients and a patient assistance foundation for uninsured patients. Learn more in our guide to saving money on Yervoy.
As of 2026, there is no generic or biosimilar version of Yervoy approved in the United States. The core patent expired in March 2025, and biosimilar development is underway (Sandoz/Henlius), but no biosimilar has reached the market yet. When one does become available, it could significantly reduce costs.
If you think Yervoy might be right for you, here's what to do:
Yervoy has given many cancer patients more time and better outcomes. Being informed about how it works and what to expect can help you get the most from your treatment.
You focus on staying healthy. We'll handle the rest.
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