| 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 | $12.13B | 19.13 | 30.56% | ― | 9.93% | 54.33% | |
76 Outperform | $10.77B | 20.63 | 9.07% | ― | 12.31% | 60.21% | |
59 Neutral | $11.47B | ― | -41.22% | ― | 864.21% | 48.12% | |
56 Neutral | $12.77B | -45.12 | -39.99% | ― | 20.39% | 34.00% | |
54 Neutral | $15.01B | -18.21 | ― | ― | 62.46% | -73.59% | |
53 Neutral | $15.86B | -4.88 | -29.32% | ― | -56.00% | -38.95% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% |
On January 12, 2026, BridgeBio Pharma used its presentation at the 44th Annual J.P. Morgan Healthcare Conference to highlight strong early commercial traction for Attruby, its ATTR-CM therapy, reporting preliminary unaudited 2025 net product revenue of $362.4 million, supported by 6,629 unique patient prescriptions from 1,632 prescribers, and to announce a new TTR amyloid-depleting antibody program expected to progress to the clinic between 2027 and 2028. The company also reported pivotal data and regulatory momentum across its late-stage pipeline, including a positive interim Phase 3 FORTIFY readout in LGMD2I/R9 that prompted FDA guidance to pursue a traditional full approval pathway and an NDA filing planned for the first half of 2026, an NDA timeline in the same period for encaleret in ADH1 amid rapid growth in diagnosed patients, a planned Phase 3 trial of encaleret in chronic hypoparathyroidism starting in summer 2026, and advancing registrational studies of infigratinib in pediatric achondroplasia and hypochondroplasia, all underpinned by approximately $587.5 million in cash and marketable securities at year-end 2025 to support continued Attruby growth and potential global launches of up to three additional medicines.
The most recent analyst rating on (BBIO) stock is a Buy with a $98.00 price target. To see the full list of analyst forecasts on BridgeBio Pharma stock, see the BBIO Stock Forecast page.
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.
The most recent analyst rating on (BBIO) stock is a Buy with a $90.00 price target. To see the full list of analyst forecasts on BridgeBio Pharma stock, see the BBIO Stock Forecast page.
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.
The most recent analyst rating on (BBIO) stock is a Buy with a $58.00 price target. To see the full list of analyst forecasts on BridgeBio Pharma stock, see the BBIO Stock Forecast page.