Breakdown | |||||
TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|
Income Statement | Total Revenue | ||||
333.45M | 290.51M | 50.70M | 0.00 | 0.00 | 0.00 | Gross Profit |
308.79M | 270.45M | 47.60M | -4.05M | -2.77M | -1.85M | EBIT |
121.06M | 65.69M | -109.73M | -145.20M | -68.28M | -33.00M | EBITDA |
130.03M | 109.91M | 17.90M | -145.20M | -65.31M | -30.32M | Net Income Common Stockholders |
123.96M | 89.16M | 10.93M | -139.97M | -69.57M | -32.17M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | ||||
616.85M | 597.52M | 532.18M | 379.17M | 438.10M | 271.26M | Total Assets |
1.07B | 1.06B | 818.36M | 558.45M | 626.29M | 310.84M | Total Debt |
9.66M | 7.26M | 8.09M | 8.93M | 8.02M | 11.55M | Net Debt |
-299.11M | -337.60M | -350.23M | -152.97M | -333.22M | -256.72M | Total Liabilities |
89.74M | 109.46M | 39.71M | 36.22M | 32.72M | 18.76M | Stockholders Equity |
984.67M | 946.38M | 778.64M | 522.23M | 593.58M | 292.08M |
Cash Flow | Free Cash Flow | ||||
129.32M | 119.18M | -100.60M | -153.55M | -116.27M | -40.93M | Operating Cash Flow |
138.50M | 123.42M | -88.80M | -100.57M | -47.94M | -26.08M | Investing Cash Flow |
-192.23M | -163.44M | 82.64M | -114.08M | -226.77M | -11.18M | Financing Cash Flow |
3.96M | 27.01M | 202.75M | 35.35M | 347.69M | 118.02M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
71 Outperform | $3.99B | 33.62 | 13.90% | ― | 247.53% | 118.34% | |
68 Neutral | $7.39B | ― | -72.73% | ― | ― | -157.53% | |
56 Neutral | $3.84B | 19.61 | -23.61% | ― | 59.15% | -1881.09% | |
55 Neutral | $5.41B | ― | -282.16% | ― | 72.16% | 9.65% | |
54 Neutral | $5.38B | 3.40 | -45.06% | 3.28% | 16.75% | -0.02% | |
50 Neutral | $8.28B | ― | -47.71% | ― | 99.19% | 48.43% | |
42 Neutral | $4.13B | ― | 435.49% | ― | 412.21% | 1.75% |
On June 2, 2025, Krystal Biotech presented a clinical update on its Phase 1/2 trial of inhaled KB707, a novel HSV-based immunotherapy for advanced lung tumors, at the ASCO Annual Meeting. The study showed that KB707 was safe, well-tolerated, and demonstrated promising anti-tumor effects, with a 36% objective response rate in heavily pre-treated non-small cell lung cancer patients. The results suggest potential synergy with immune checkpoint inhibitors, and further evaluation is ongoing.
The most recent analyst rating on (KRYS) stock is a Buy with a $208.00 price target. To see the full list of analyst forecasts on Krystal Biotech stock, see the KRYS Stock Forecast page.
On May 16, 2025, Krystal Biotech held its Annual Meeting of Stockholders where key decisions were made, including the election of Class II directors and the ratification of KPMG LLP as the independent registered public accounting firm for 2025. Additionally, stockholders approved the compensation of the company’s named executive officers for the fiscal year 2024, reflecting confidence in the company’s leadership and strategic direction.
The most recent analyst rating on (KRYS) stock is a Buy with a $208.00 price target. To see the full list of analyst forecasts on Krystal Biotech stock, see the KRYS Stock Forecast page.
On May 9, 2025, Krystal Biotech presented a poster at the Society for Investigative Dermatology Annual Meeting, detailing the expansion of its HSV-1-based gene therapy platform to treat Hailey-Hailey and Darier diseases. The studies demonstrated that the company’s gene therapy vectors, KB111 and KB112, can effectively transduce keratinocytes and express ATPases with minimal toxicity, indicating promising potential for treating these rare skin conditions.
The most recent analyst rating on (KRYS) stock is a Buy with a $208.00 price target. To see the full list of analyst forecasts on Krystal Biotech stock, see the KRYS Stock Forecast page.
On May 5, 2025, Krystal Biotech presented research at the ARVO Annual Meeting showcasing their HSV-1-based gene therapy vector, KB801, which demonstrated sustained nerve growth factor expression in wounded murine corneas. This development highlights KB801’s potential as a safe and effective topical treatment for neurotrophic keratitis, offering a less burdensome alternative to the current treatment, cenegermin-bkbj, which requires frequent dosing.
On April 23, 2025, the European Commission approved VYJUVEK® for treating dystrophic epidermolysis bullosa (DEB) in Europe, marking it as the first corrective medicine for DEB in the region. This approval allows flexible dosing at home or in healthcare settings and is expected to significantly impact Krystal Biotech‘s market presence in Europe, with plans for a launch in Germany by mid-2025.