| Breakdown | Dec 2025 | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 |
|---|---|---|---|---|---|
Income Statement | |||||
| Total Revenue | 502.08M | 221.90M | 9.30M | 77.65M | 69.72M |
| Gross Profit | 473.81M | 218.02M | 6.86M | 74.21M | 66.60M |
| EBITDA | -672.88M | -436.83M | -565.47M | -397.44M | -533.83M |
| Net Income | -729.31M | -535.76M | -643.20M | -481.18M | -562.54M |
Balance Sheet | |||||
| Total Assets | 936.02M | 919.34M | 546.38M | 623.04M | 1.01B |
| Cash, Cash Equivalents and Short-Term Investments | 587.48M | 681.10M | 434.88M | 471.92M | 836.66M |
| Total Debt | 2.73B | 1.73B | 1.74B | 1.72B | 1.73B |
| Total Liabilities | 3.01B | 2.38B | 1.89B | 1.87B | 1.88B |
| Stockholders Equity | -2.08B | -1.47B | -1.35B | -1.25B | -870.41M |
Cash Flow | |||||
| Free Cash Flow | -447.01M | -521.66M | -529.03M | -425.81M | -546.18M |
| Operating Cash Flow | -445.91M | -520.73M | -527.72M | -419.49M | -497.93M |
| Investing Cash Flow | -24.49M | 60.78M | 54.03M | 453.15M | -200.83M |
| Financing Cash Flow | 359.29M | 748.46M | 451.54M | -13.13M | 736.45M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
76 Outperform | $10.72B | 12.10 | 35.53% | ― | 9.93% | 54.33% | |
74 Outperform | $11.65B | 32.67 | 5.94% | ― | 12.31% | 60.21% | |
58 Neutral | $21.26B | -4.07 | -28.87% | ― | -56.00% | -38.95% | |
55 Neutral | $10.08B | ― | -42.49% | ― | 864.21% | 48.12% | |
53 Neutral | $12.42B | -33.22 | -70.72% | ― | 20.39% | 34.00% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
50 Neutral | $12.83B | ― | ― | ― | 62.46% | -73.59% |
On February 12, 2026, BridgeBio reported positive topline results from its global Phase 3 PROPEL 3 trial of oral infigratinib in children with achondroplasia, showing a highly significant improvement in annualized height velocity over placebo at Week 52 and the highest absolute growth rates yet seen in a randomized achondroplasia study. The trial also met a key secondary endpoint on height Z‑score and, in children under eight, delivered the first statistically significant improvement in body proportionality versus placebo for any therapy in this condition.
Infigratinib was well tolerated, with no drug‑related discontinuations or serious adverse events and only mild, transient hyperphosphatemia, and no safety signals typically associated with FGFR1/2 inhibition or CNP analogues. On the back of these data, BridgeBio plans regulatory submissions for achondroplasia in the second half of 2026 and is accelerating Phase 3 development of infigratinib in hypochondroplasia, moves that could broaden treatment options and reinforce its position in the emerging market for targeted, oral therapies for skeletal dysplasias.
The most recent analyst rating on (BBIO) stock is a Buy with a $100.00 price target. To see the full list of analyst forecasts on BridgeBio Pharma stock, see the BBIO Stock Forecast page.
On January 21, 2026, BridgeBio Pharma, Inc. issued $632.5 million of 0.75% Convertible Senior Notes due 2033 in a Rule 144A private placement to qualified institutional buyers, including $82.5 million issued pursuant to the initial purchasers’ option, generating approximately $619.3 million in net proceeds. The senior unsecured notes, which carry semiannual interest and are convertible into cash, common stock or a combination at BridgeBio’s election, are intended primarily to refinance or prefund a portion of the company’s 2.50% Convertible Senior Notes due 2027 and to support general corporate purposes, while maintaining pari passu ranking with BridgeBio’s existing convertible notes and extending the company’s debt maturity profile. Concurrent with the note offering’s closing on January 21, 2026, BridgeBio used about $82.5 million of cash on hand to repurchase 1,081,825 shares of its common stock in privately negotiated transactions at $76.26 per share, a move that formed part of its broader long-term debt management strategy aimed at strengthening the balance sheet, lowering interest expense, reducing dilution, and significantly extending debt maturities, with potential effects on the trading dynamics of both its stock and the new notes.
The most recent analyst rating on (BBIO) stock is a Buy with a $88.00 price target. To see the full list of analyst forecasts on BridgeBio Pharma stock, see the BBIO Stock Forecast page.
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.