| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 183.40M | 76.99M | 237.00K | 596.00K | 1.39M | 253.00K |
| Gross Profit | 158.11M | 75.74M | 237.00K | 596.00K | 1.39M | -49.80M |
| EBITDA | -44.86M | -154.85M | -174.78M | -134.15M | -111.59M | -76.75M |
| Net Income | -79.99M | -174.57M | -184.13M | -141.90M | -116.11M | -75.62M |
Balance Sheet | ||||||
| Total Assets | 567.38M | 593.78M | 394.08M | 190.57M | 226.03M | 270.73M |
| Cash, Cash Equivalents and Short-Term Investments | 380.53M | 406.57M | 333.70M | 172.75M | 183.72M | 196.28M |
| Total Debt | 121.92M | 121.72M | 85.90M | 55.75M | 55.00M | 29.72M |
| Total Liabilities | 318.68M | 313.46M | 146.13M | 110.58M | 99.62M | 59.78M |
| Stockholders Equity | 248.71M | 280.32M | 247.95M | 80.00M | 126.42M | 210.95M |
Cash Flow | ||||||
| Free Cash Flow | -132.82M | -219.30M | -168.57M | -127.81M | -95.76M | -67.05M |
| Operating Cash Flow | -132.91M | -218.62M | -167.74M | -127.38M | -95.56M | -66.65M |
| Investing Cash Flow | -17.41M | -106.00M | -180.32M | 62.07M | 71.95M | -105.32M |
| Financing Cash Flow | 168.05M | 334.37M | 362.02M | 87.26M | 48.56M | 168.35M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
52 Neutral | $1.15B | ― | -308.02% | ― | 196.42% | 53.92% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
48 Neutral | $1.69B | ― | -129.32% | ― | 597.19% | 0.45% | |
47 Neutral | $760.31M | 4.70 | 75.08% | ― | 1647.67% | ― | |
45 Neutral | $759.64M | ― | -29.57% | ― | 522.13% | 62.68% | |
40 Underperform | $1.70B | ― | -165.27% | ― | -44.90% | 11.49% | |
39 Underperform | $759.04M | -4.66 | -51.98% | ― | ― | -75.31% |
Geron Corporation is a commercial-stage biopharmaceutical company focused on developing innovative therapies for blood cancer, with its flagship product RYTELO, a telomerase inhibitor, approved for certain anemic conditions. In the third quarter of 2025, Geron Corporation reported a significant increase in net product revenue from RYTELO, reaching $47.2 million, despite a slight decline in demand. The company completed patient enrollment for its Phase 3 IMpactMF clinical trial and strengthened its leadership team, aiming to enhance commercial execution and expand its market presence. Key financial metrics showed a reduction in net loss compared to the previous year, with total revenues significantly increasing from $28.3 million to $47.2 million. Operating expenses rose slightly due to increased investment in research and development and marketing. Looking ahead, Geron Corporation remains optimistic about its strategic initiatives and financial position, with plans to continue expanding RYTELO’s reach and advancing its clinical pipeline, supported by a strong cash position.
The recent earnings call of Geron Corporation presented a mixed sentiment among stakeholders. While there were positive developments such as an increase in prescribing accounts and new patient starts, the company also faced challenges including declining demand and the need for greater awareness and education regarding RYTELO’s use in earlier treatment lines.
On October 10, 2025, Geron Corporation announced the resignation of board member Dr. Gaurav Aggarwal and the decision of Dr. V. Bryan Lawlis not to stand for re-election at the 2026 Annual Meeting. Additionally, on October 15, 2025, executives Andrew J. Grethlein and Jim Ziegler departed from their roles, with Grethlein transitioning to a consulting role to assist with the transition. On October 13, 2025, Geron announced several executive leadership transitions, appointing Ahmed ElNawawi as the new Executive Vice President, Chief Commercial Officer, along with three other seasoned executives to strengthen its leadership team. These changes aim to align the company’s leadership structure with its strategic priorities, focusing on driving growth and maximizing the potential of RYTELO®.
The most recent analyst rating on (GERN) stock is a Hold with a $1.50 price target. To see the full list of analyst forecasts on Geron stock, see the GERN Stock Forecast page.
Geron Corporation is conducting a Phase 3 clinical study titled ‘A Randomized Open-Label, Phase 3 Study to Evaluate Imetelstat (GRN163L) Versus Best Available Therapy (BAT) in Patients With Intermediate-2 or High-risk Myelofibrosis (MF) Relapsed / Refractory (R/R) to Janus Kinase (JAK) Inhibitor.’ The study aims to assess the overall survival of participants with intermediate-2 or high-risk Myelofibrosis who have not responded to JAK-Inhibitor treatment, highlighting its significance in addressing unmet medical needs in this patient population.
Geron Corporation is conducting a Phase 3 clinical study titled A Randomized Open-Label, Phase 3 Study to Evaluate Imetelstat (GRN163L) Versus Best Available Therapy (BAT) in Patients With Intermediate-2 or High-risk Myelofibrosis (MF) Relapsed / Refractory (R/R) to Janus Kinase (JAK) Inhibitor. The study aims to assess the overall survival of participants receiving imetelstat compared to those receiving the best available therapy, targeting patients with intermediate-2 or high-risk MF who have not responded to JAK-inhibitor treatment.
Study Overview: Geron Corporation is conducting a Phase 3 clinical study titled A Randomized Open-Label, Phase 3 Study to Evaluate Imetelstat (GRN163L) Versus Best Available Therapy (BAT) in Patients With Intermediate-2 or High-risk Myelofibrosis (MF) Relapsed / Refractory (R/R) to Janus Kinase (JAK) Inhibitor. The study aims to assess the overall survival of participants treated with imetelstat compared to BAT in patients who have not responded to JAK-inhibitor treatment, highlighting its potential significance in advancing treatment options for this patient group.