BridgeBio Pharma, Inc. (BBIO) Stock Price & How to Invest

Short answer

BBIO is BridgeBio Pharma, a commercial-stage biopharma whose value hinges on Attruby (acoramidis), a fast-growing heart drug for ATTR-CM, plus a genetic-disease pipeline. Investing in BBIO is a bet that Attruby keeps taking share from Pfizer and Alnylam and that new launches diversify the story before the loss-making phase ends.

BBIO stock price

As of 2026-07-09, BridgeBio Pharma, Inc. (BBIO) last closed at $90.17, up 94.9% over the past year. Over the past 52 weeks it has traded between $44.81 and $90.17.

BBIO last close
$90.17
1 day
+15.12%
1 month
+33.23%
1 year
+94.88%
52-week range
$44.81 to $90.17
Last close
2026-07-09

Prices are daily closing prices from Yahoo Finance and may be delayed. For the live quote, check your broker or BridgeBio Pharma, Inc.'s investor relations page. Walnut is informational, not investment advice.

What does BridgeBio Pharma, Inc. (BBIO) do?

BridgeBio Pharma (NASDAQ: BBIO) is a Palo Alto-based biopharmaceutical company focused on genetic diseases and genetically driven cancers. Its commercial engine is Attruby (acoramidis), an oral TTR stabilizer approved by the FDA in November 2024 for transthyretin amyloid cardiomyopathy (ATTR-CM), a progressive and often underdiagnosed heart condition. Attruby competes in a market long dominated by Pfizer's tafamidis franchise, and BridgeBio has been rapidly building prescriber and patient uptake since launch.

The investment picture is a high-growth, still-unprofitable commercial biopharma. Revenue is scaling quickly (Attruby net product revenue grew sharply year over year), but the company continues to report large net losses as it invests in commercialization and R&D. Beyond Attruby, BridgeBio is trying to diversify with multiple near-term regulatory filings (BBP-418 in limb-girdle muscular dystrophy, encaleret in ADH1, and infigratinib in achondroplasia). The stock trades at a premium valuation that prices in continued Attruby momentum and pipeline success, so results and FDA decisions matter a great deal.

What's driving BridgeBio Pharma, Inc. (BBIO)?

1. Attruby (acoramidis) commercial ramp

Attruby net product revenue reached roughly $180 million in Q1 2026, up dramatically from a year earlier, as prescriptions and prescriber counts expanded. BridgeBio points to near-complete TTR stabilization and a broad label as differentiators versus Pfizer's tafamidis. Continued share gains in the large, underdiagnosed ATTR-CM market are the core driver of the story.

2. Pipeline diversification and 2026 filings

BridgeBio is pushing to become more than a one-drug company with three genetic-disease programs advancing toward the market. BBP-418 for LGMD2I/R9 has an FDA decision targeted for late November 2026, encaleret for ADH1 was filed in May 2026, and infigratinib for achondroplasia is slated for filing later in 2026. Each approval would add a potential first-in-class launch.

3. Improving financial profile and balance sheet

Rising Attruby revenue plus royalty income has strengthened the balance sheet, with cash and marketable securities near $940 million as of Q1 2026. Management authorized a $500 million share repurchase program in May 2026, signaling confidence in intrinsic value. The path toward operating leverage as revenue outgrows fixed commercial costs is a key part of the bull case.

4. Large under-penetrated ATTR-CM market

ATTR-CM remains widely underdiagnosed, so improved awareness and diagnosis can expand the treated population for all approved therapies. BridgeBio benefits from being one of only a handful of stabilizer options, alongside Pfizer and Alnylam. Growth in new diagnoses is a tailwind independent of head-to-head share shifts.

What are the risks to BridgeBio Pharma, Inc. (BBIO)?

The dominant risk is concentration: Attruby is BridgeBio's only approved commercial product, so near-term performance is highly dependent on a single therapy in a competitive market. Pfizer's entrenched tafamidis franchise and Alnylam's vutrisiran (Amvuttra) are well-funded rivals fighting for the same patients. Any FDA delay, rejection, request for more data, or narrower-than-expected label for BBP-418, encaleret, or infigratinib would push out the diversification timeline. The company is still deeply unprofitable, with large trailing net losses and ongoing cash burn on R&D and commercialization. Pricing pressure, slower diagnosis growth, or a valuation that already embeds heavy optimism could all weigh on the shares.

How is BridgeBio Pharma, Inc. (BBIO) valued? (approximate, Q1 2026)

A simple financial snapshot. These are approximations and refresh quarterly; for current figures see BridgeBio Pharma, Inc.'s investor relations page or your broker.

  • Revenue (Q1 2026): ~$195M
  • Attruby net revenue (Q1 2026): ~$181M
  • Revenue (TTM): ~$500M-$580M
  • Net income (TTM): ~-$733M
  • Cash and marketable securities: ~$940M
  • Market cap: ~$14B-$15B

BBIO trades at a rich multiple of trailing revenue, reflecting expectations for continued Attruby growth and pipeline launches rather than current profits. Revenue is expanding rapidly, but the company still posts large net losses as it invests in commercialization and R&D. A $500 million buyback authorized in May 2026 and a cash position near $940 million give it near-term financial flexibility.

Who competes with BridgeBio Pharma, Inc. (BBIO)?

ATTR-CM stabilizers and RNAi therapies

Pfizer's tafamidis franchise (Vyndaqel/Vyndamax) is the entrenched incumbent approved since 2019, and Alnylam's vutrisiran (Amvuttra) competes with an RNAi approach. These are the direct rivals to Attruby for the same heart-amyloidosis patients.

Rare and genetic-disease biopharma

BridgeBio competes for pipeline value and capital with other rare-disease developers such as Alnylam, Ionis, Ultragenyx, and BioMarin, which pursue genetically defined conditions and, in some cases, overlapping indications like achondroplasia and skeletal disorders.

Large-cap pharma with cardiovascular and rare-disease reach

Diversified players including Pfizer, AstraZeneca, and Novartis have the scale, sales infrastructure, and cash to expand in cardiovascular and rare-disease markets, representing broader competitive and partnership pressure on a smaller company like BridgeBio.

How to invest in BridgeBio Pharma, Inc. (BBIO)

There are three common ways to get BBIO exposure. Buy shares (or fractional shares) directly at any major broker. Hold an ETF that includes it, which spreads the position across many companies. Or build it into a focused thematic basket, so BBIO sits alongside other stocks that express the same thesis.

Walnut takes the basket route. Describe a thesis where BBIO fits (for example “AI infrastructure” or “dividend-growth large-caps”) and the AI proposes 5 to 6 constituents with target weights. You review the plan and fund it through your own broker when you're ready.

The bottom line on BridgeBio Pharma, Inc. (BBIO)

BBIO is a single-product growth-biopharma story riding Attruby's rapid ramp, with pipeline launches and profitability still ahead of it.

More on BridgeBio Pharma, Inc. (BBIO)

Whether BBIO is worth buying today depends more on your time horizon and what you already hold than on any single call. We walk through valuation, what would have to go right, and the risks in is BBIO a buy?, and where the stock could go from here in the BBIO stock forecast.

For income investors, whether BBIO pays a dividend and how the payout looks is covered in does BBIO pay a dividend?

Build a basket around BBIO with Walnut

Use BridgeBio Pharma, Inc. as one constituent in a thematic basket Walnut's AI helps you assemble. Describe a thesis you believe in, the AI proposes the holdings and weights, and you approve before any broker order.

FAQ

What does BridgeBio Pharma (BBIO) do?

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BridgeBio is a biopharmaceutical company that develops medicines for genetic diseases and genetically driven cancers. Its lead product, Attruby (acoramidis), treats transthyretin amyloid cardiomyopathy (ATTR-CM), a progressive heart condition, and it has additional rare-disease programs in development.

What is Attruby and why does it matter to BBIO?

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Attruby (acoramidis) is BridgeBio's FDA-approved oral TTR stabilizer for ATTR-CM, launched in December 2024. It is the company's only approved commercial product and the primary driver of revenue, so its uptake against Pfizer and Alnylam largely defines BBIO's near-term financial performance.

Is BridgeBio profitable?

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No. Despite rapidly growing Attruby revenue, BridgeBio still reports large net losses, with trailing net income around negative $733 million, as it spends heavily on commercialization and R&D. Reaching sustained profitability depends on continued revenue growth outpacing operating costs.

How fast is BBIO's revenue growing?

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Very fast off a small base. Q1 2026 total revenue was about $195 million, with Attruby net product revenue near $181 million, up roughly 392% year over year. Trailing twelve-month revenue is in the ~$500 million to ~$580 million range depending on the source and period.

Who are BridgeBio's main competitors?

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In ATTR-CM, Attruby competes with Pfizer's tafamidis franchise (Vyndaqel/Vyndamax) and Alnylam's vutrisiran (Amvuttra). More broadly, BridgeBio competes with rare-disease developers such as Ionis, Ultragenyx, and BioMarin, and with large-cap pharma in cardiovascular and genetic-disease markets.

What are BBIO's key upcoming catalysts?

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BridgeBio has several near-term regulatory events: an FDA decision on BBP-418 for LGMD2I/R9 targeted for late November 2026, encaleret for ADH1 filed in May 2026, and infigratinib for achondroplasia expected to be filed later in 2026. These filings aim to diversify beyond Attruby.

What are the biggest risks for BBIO?

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The main risk is product concentration, since Attruby is BridgeBio's only approved drug in a competitive market against Pfizer and Alnylam. Other risks include FDA delays or rejections for pipeline candidates, continued cash burn and net losses, pricing pressure, and a premium valuation that assumes strong future growth.

How much cash does BridgeBio have?

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As of the end of Q1 2026, BridgeBio reported cash, cash equivalents, and marketable securities of roughly $940 million. The company also authorized a $500 million share repurchase program in May 2026, giving it near-term financial flexibility while it continues to invest in growth.

Walnut is informational, not investment advice. Financial figures on this page are approximations; always verify current numbers with BridgeBio Pharma, Inc.'s investor relations page or your broker before making investment decisions.