Sometimes in biotech, the story is complicated. This isn't one of those times. ImmunityBio, Inc. (IBRX) just reported a 700% revenue jump, and investors are understandably excited about it. Shares popped over 26% on Thursday as the company unveiled numbers that show its flagship bladder cancer drug is actually gaining real commercial traction.
The Numbers Tell a Growth Story
Let's start with the headline figure: ImmunityBio announced preliminary net product revenue for Anktiva reached approximately $113 million for fiscal 2025. That's not just good—it's a 700% increase year-over-year. For context, Anktiva is the first FDA-approved immunotherapy specifically for non-muscle invasive bladder cancer carcinoma in situ (CIS), which makes it a pretty big deal in oncology circles.
The fourth quarter alone brought in about $38.3 million, topping the previous quarter's $31.8 million. That's a 20% sequential increase and a 431% year-over-year jump. But here's the really interesting part: unit sales volume for Anktiva increased 750% in 2025 compared to 2024. That's not just price increases or accounting magic—that's actual doctors prescribing more drug to more patients.
"We delivered strong quarter-over-quarter revenue growth, reflecting accelerating adoption of Anktiva and the continued execution of our commercial strategy," said Richard Adcock, President and CEO of ImmunityBio. When a CEO talks about "accelerating adoption," it's usually corporate-speak, but in this case the numbers back it up.
The company ended the quarter sitting on an estimated $242.8 million in cash, cash equivalents, and marketable securities, which gives them some runway to keep building out their commercial operations.
Beyond Bladder Cancer
On Tuesday, ImmunityBio shared fresh data that could expand Anktiva's potential beyond its current indication. The company presented results from two studies—QUILT-2.023 and QUILT-3.055—focused on non-small cell lung cancer. Across 151 patients spanning first-line, second-line, and later-line disease, Anktiva demonstrated statistically significant immune restoration and showed a consistent link between lymphocyte recovery and improved survival in checkpoint-experienced patients.
Translation: the drug might help patients whose immune systems have been worn down by previous cancer treatments, which could open up entirely new markets if the clinical program continues to deliver.




