| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 82.56M | 14.74M | 622.00K | 240.00K | 934.00K | 605.00K |
| Gross Profit | 78.23M | 14.74M | 622.00K | 240.00K | 934.00K | 605.00K |
| EBITDA | -232.64M | -264.43M | -478.66M | -351.88M | -320.75M | -204.22M |
| Net Income | -348.62M | -413.56M | -583.20M | -416.57M | -346.79M | -221.85M |
Balance Sheet | ||||||
| Total Assets | 0.00 | 382.93M | 504.45M | 362.36M | 468.91M | 221.38M |
| Cash, Cash Equivalents and Short-Term Investments | 153.66M | 149.81M | 266.46M | 107.18M | 317.12M | 96.06M |
| Total Debt | 0.00 | 504.17M | 726.72M | 723.77M | 645.66M | 275.55M |
| Total Liabilities | 569.82M | 871.06M | 1.09B | 812.18M | 712.82M | 339.87M |
| Stockholders Equity | -569.82M | -489.10M | -586.99M | -447.33M | -242.17M | -119.81M |
Cash Flow | ||||||
| Free Cash Flow | -324.01M | -398.12M | -397.34M | -415.67M | -307.98M | -173.39M |
| Operating Cash Flow | -319.70M | -391.24M | -366.76M | -337.51M | -274.42M | -171.72M |
| Investing Cash Flow | -183.54M | -12.25M | -30.47M | 27.30M | -84.89M | -19.81M |
| Financing Cash Flow | 452.28M | 281.63M | 558.34M | 233.61M | 505.44M | 150.68M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
74 Outperform | $2.85B | 13.52 | 27.52% | ― | 25.56% | 44.42% | |
60 Neutral | $3.27B | -75.40 | -28.17% | ― | 129.21% | 80.35% | |
56 Neutral | $5.51B | -9.67 | -95.93% | ― | ― | -27.70% | |
53 Neutral | $3.59B | ― | -47.19% | ― | -84.07% | -157.71% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
49 Neutral | $2.97B | ― | ― | ― | 1025.95% | 52.91% | |
47 Neutral | $1.67B | -56.71 | -7.52% | ― | 27.51% | 38.72% |
On January 14, 2026, ImmunityBio announced that the Saudi Food and Drug Authority granted accelerated approval of ANKTIVA® (nogapendekin alfa inbakicept) in combination with immune checkpoint inhibitors for adult patients with metastatic non-small cell lung cancer whose disease has progressed following standard-of-care therapy, marking the first global approval for a subcutaneously administered IL-15 receptor superagonist and the first approval of this chemotherapy-free, NK- and T-cell–activating immunotherapy for this indication. On the same date, the SFDA also granted accelerated approval for ANKTIVA® plus Bacillus Calmette-Guérin (BCG) to treat adult patients with BCG-unresponsive non-muscle invasive bladder cancer carcinoma in situ, with or without papillary disease, underscoring ImmunityBio’s push into Middle East and North Africa oncology markets, supported by plans for a regional office in Saudi Arabia and a commercial partnership with BioPharma Cigalah; these approvals, based on clinical data from the QUILT trial program and backed by patents extending into 2032–2039, enhance the company’s international footprint and position its ANKTIVA-based regimens as a new chemotherapy-free backbone in immunotherapy for difficult-to-treat cancers in a region with significant unmet need.
The most recent analyst rating on (IBRX) stock is a Buy with a $8.00 price target. To see the full list of analyst forecasts on ImmunityBio stock, see the IBRX Stock Forecast page.
On December 10, 2025, ImmunityBio, Inc. appointed Bruce Wendel to its Board of Directors, effective December 12, 2025, with his term expiring at the 2026 annual stockholders meeting. Wendel, recognized as an independent director, brings extensive experience from his previous roles in the pharmaceutical industry, including leadership positions at ProMetic Biosciences Ltd. and Hepalink USA. His appointment is expected to strengthen ImmunityBio’s strategic direction and industry positioning.
The most recent analyst rating on (IBRX) stock is a Buy with a $5.00 price target. To see the full list of analyst forecasts on ImmunityBio stock, see the IBRX Stock Forecast page.
On December 12, 2025, ImmunityBio announced that the European Medicines Agency recommended conditional marketing authorization for ANKTIVA® in combination with BCG for treating non-muscle invasive bladder cancer (NMIBC) carcinoma in situ in Europe. This recommendation marks the first immunotherapy for NMIBC with carcinoma in situ to receive such a positive recommendation in Europe, addressing a significant unmet need for patients unresponsive to BCG, whose primary option has been bladder removal surgery. The decision is based on a single-arm trial showing promising response rates, and it highlights ImmunityBio’s efforts to expand access to innovative treatments in Europe, potentially impacting the company’s market positioning and offering new hope for patients.
The most recent analyst rating on (IBRX) stock is a Buy with a $5.00 price target. To see the full list of analyst forecasts on ImmunityBio stock, see the IBRX Stock Forecast page.