| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 353.78M | 221.90M | 9.30M | 77.65M | 69.72M | 8.25M |
| Gross Profit | 338.84M | 218.02M | 6.86M | 74.21M | 66.60M | 8.25M |
| EBITDA | -677.28M | -436.83M | -565.47M | -397.44M | -533.83M | -467.38M |
| Net Income | -797.12M | -535.76M | -643.20M | -481.18M | -562.54M | -448.72M |
Balance Sheet | ||||||
| Total Assets | 998.25M | 919.34M | 546.38M | 623.04M | 1.01B | 703.59M |
| Cash, Cash Equivalents and Short-Term Investments | 645.94M | 681.10M | 434.88M | 471.92M | 836.66M | 607.09M |
| Total Debt | 1.86B | 1.73B | 1.74B | 1.72B | 1.73B | 495.79M |
| Total Liabilities | 2.92B | 2.38B | 1.89B | 1.87B | 1.88B | 595.70M |
| Stockholders Equity | -1.93B | -1.47B | -1.35B | -1.25B | -870.41M | 57.91M |
Cash Flow | ||||||
| Free Cash Flow | -595.21M | -521.66M | -529.03M | -425.81M | -546.18M | -407.23M |
| Operating Cash Flow | -584.82M | -520.73M | -527.72M | -419.49M | -497.93M | -399.71M |
| Investing Cash Flow | -13.37M | 60.78M | 54.03M | 453.15M | -200.83M | -52.99M |
| Financing Cash Flow | 835.41M | 748.46M | 451.54M | -13.13M | 736.45M | 447.19M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
78 Outperform | $11.26B | 17.92 | 30.56% | ― | 9.93% | 54.33% | |
77 Outperform | $9.95B | 19.46 | 9.07% | ― | 12.31% | 60.21% | |
61 Neutral | $12.48B | -45.36 | -39.99% | ― | 20.39% | 34.00% | |
59 Neutral | $14.26B | -17.71 | ― | ― | 62.46% | -73.59% | |
58 Neutral | $11.92B | ― | -29.32% | ― | -56.00% | -38.95% | |
56 Neutral | $12.40B | -41.85 | -41.22% | ― | 864.21% | 48.12% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% |
BridgeBio Pharma announced positive results from its Phase 3 CALIBRATE study of encaleret for treating autosomal dominant hypocalcemia type 1 (ADH1) on October 29, 2025. The study met all primary and key secondary endpoints, showing significant improvements in calcium and parathyroid hormone levels compared to conventional therapy. Encaleret was well-tolerated, with plans for a New Drug Application submission in 2026. The results suggest encaleret could become a new standard of care for ADH1, potentially impacting the lives of patients with this genetic condition.
On October 27, 2025, BridgeBio Pharma announced positive results from its Phase 3 FORTIFY study of BBP-418, a treatment for limb-girdle muscular dystrophy type 2I/R9 (LGMD2I/R9). The study showed significant improvements in motor and pulmonary functions, with a well-tolerated safety profile, marking a potential breakthrough for a disease with no specific treatments. The company plans to file for FDA approval in the first half of 2026, which could position BBP-418 as the first therapy to alter the course of this debilitating condition.