BridgeBio Pharma, Inc. (BBIO) is a Healthcare stock trading at $81.08 (as of 2026-08-24), with a market capitalization of $15.85B. Figures are sourced from first-party U.S. SEC EDGAR filings and market data.
BridgeBio Pharma, Inc. engages in the discovery, development, and delivery of various medicines for genetic diseases. The company has a pipeline of 30 development programs that include product candidates ranging from early discovery to late-stage development. Its products in development programs include AG10 and BBP-265, a small molecule stabilizer of transthyretin, or TTR that is in Phase 3 clinical trial for the treatment of TTR amyloidosis-cardiomyopathy, or ATTR-CM; BBP-831, a small molecule selective FGFR1-3 inhibitor, which is Phase 2 clinical trial to treat achondroplasia in pediatric patients; and BBP-631, an AAV5 gene transfer product candidate that is in Phase 2 clinical trial for the treatment of congenital adrenal hyperplasia, or CAH, driven by 21-hydroxylase deficiency, or 21OHD. The company also develops Encaleret, a small molecule antagonist of the calcium sensing receptor, or CaSR, which is in phase 2 proof-of-concept clinical trial for Autosomal Dominant Hypocalcemia Type 1, or ADH1; and BBP-711 for the treatment of hyperoxaluria, as well as patients suffering from recurrent kidney stones. In addition, it engages in developing products for Mendelian, oncology, and gene therapy diseases. BridgeBio Pharma, Inc. has license and collaboration agreements with the Leland Stanford Junior University; and The Regents of the University of California; Leidos Biomedical Research, Inc. The company was founded in 2015 and is headquartered in Palo Alto, California.
BridgeBio develops small-molecule drugs for rare genetic diseases and sells approved products to patients at high per-prescription prices. With roughly 30 pipeline programs against one or two approved drugs, it is a pre-profit orphan franchise where clinical readouts matter more than current cash flow.
High-priced orphan drugs generate 94% gross margins, but funding roughly 30 simultaneous R&D programs absorbs every dollar of that gross profit, so clinical approval milestones are the actual profit engine until the pipeline narrows.
Business quality (Weak): Pre-profit biotech: 94% gross margin confirms real drug economics, but -44% operating margin and -661% ROE show the company is still deeply in the spend-down phase of a large pipeline. Grade: Weak on current financials, though the 120% revenue growth signals a turning point if products continue to scale.
| Price | $81.08 |
| Market Cap | $15.85B |
| Price / Sales | 22.23 |
| FCF Yield | -2.7% |
| Revenue (TTM) | $502.08M |
| Net Margin | -146.0% |
| Revenue Growth (YoY) | 120.4% |
| EPS Growth (YoY) | -17.9% |
| FCF Growth (YoY) | -12.0% |
| Altman Z-Score | -3.24 (distress) |
| Piotroski F-Score | 2/9 (weak) |
| Sector P/E (Healthcare) | 21.7 |
| Industry P/E (Pharmaceutical Products) | 17.1 |
| Top Institutional Holder | VANGUARD GROUP INC ($1.29B) |
| Institutional Holders Tracked | 10 |
| Congressional Trades (recent) | 6 |
| Sector | Healthcare |
| Industry | Pharmaceutical Products |
| CEO | Neil Kumar |
| Employees | 725 |
| Country | US |
| IPO Date | 2019-06-27 |
Data as of 2026-08-24.
Figures sourced from U.S. Securities and Exchange Commission (SEC EDGAR) filings and market data. Not personalized investment advice.