Highlights
- Total third-quarter 2026 Revenue reached US$353.2 million, up from US$120.7 million in the same quarter of 2025.
- U.S. Attruby net product revenue climbed to US$253.2 million, rising about US$31 million from the preceding quarter.
- Net loss narrowed to US$60.5 million from US$184.9 million, while net loss per share improved to US$0.42.
- BridgeBio holds three FDA decision dates: BBP-418 in November 2026, infigratinib in February 2027 and encaleret in May 2027.
BridgeBio Pharma, Inc. (NASDAQ:BBIO) is heading into the last weeks of 2026 with its first approved medicine carrying most of its revenue and a US regulatory decision on its second product less than a month away.
On 29 October 2026, the rare-disease drug developer reported third-quarter revenue of US$353.2 million, close to three times the prior-year level, driven by Attruby (acoramidis), its treatment for transthyretin amyloid cardiomyopathy (ATTR-CM). The company also reiterated a 27 November 2026 FDA target action date for BBP-418 in limb-girdle muscular dystrophy type 2I/R9 (LGMD2I/R9).
Attruby Carries the Revenue Line
U.S. Attruby net product revenue was US$253.2 million in Q3 2026, up US$145.2 million year on year and about US$31 million on the second quarter. Management attributed the growth to treatment-naive patients, with both the number of new starts and their share of new starts rising.
Royalty revenue, mainly tied to Beyonttra sales in the EU and Japan, rose to US$20.5 million from US$4.3 million. License and services revenue reached US$79.3 million, including a US$75.0 million sales milestone from Bayer recognized in the quarter. For the nine months to 30 September 2026, total revenue was US$791.4 million, against US$347.9 million a year earlier.
Operating Loss Shrinks as Launch Spending Grows
Total operating costs and expenses increased to US$364.8 million from US$265.9 million. Research and Development expense rose to US$143.5 million, while selling, general and administrative expense climbed to US$200.9 million. Even so, the loss from operations narrowed sharply to US$11.6 million from US$145.2 million.
The GAAP net loss was US$60.5 million. After US$26.3 million of preferred stock dividends and accretion, the net loss attributable to common stockholders was US$83.0 million, or US$0.42 per share, compared with US$0.95 per share a year earlier.
Cash, cash equivalents and marketable securities stood at US$1.54 billion on 30 September 2026, up from US$587.5 million at the end of 2025. During the first nine months of the year, BridgeBio issued US$632.5 million of 2033 notes and US$933.9 million of preferred stock and repurchased US$252.5 million of common stock. Management stated that its cash position fully funds its three launches and expansion indications.
Three FDA Decisions Lined Up Through May 2027
BBP-418 for LGMD2I/R9 has a PDUFA date of 27 November 2026 after its new drug application was accepted with Priority Review on 27 May 2026, and no advisory committee meeting is planned. The company has identified more than 500 US patients with the condition.
Oral infigratinib for achondroplasia has a PDUFA date of 4 February 2027, and encaleret for autosomal dominant hypocalcemia type 1 (ADH1) has a PDUFA date of 8 May 2027. Both are also under review in the EU, where the company sees potential approvals in the second half of 2027. A Phase 3 study of encaleret in chronic hypoparathyroidism has dosed its first participant, with topline data expected in early 2028.






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