For Q1 FY2026 (ended March 31, 2026), BridgeBio Pharma reported revenue of $194.5 million, up 66.8% year-over-year. Operating loss was $106.0 million, slightly worse than the prior year. Diluted EPS was -$0.84, improving 4.5% from -$0.88. The company held $879.9 million in cash, with long-term debt of $2.65 billion and negative equity of $2.28 billion.
•Revenue grew 66.8% YoY to $194.5 million.
•Operating loss widened slightly to $106.0 million.
•Diluted EPS improved to -$0.84 from -$0.88.
•Cash balance was $879.9 million; long-term debt stood at $2.65 billion.
Informational summary based on SEC XBRL figures · generated by deepseek-v4-flash. Not investment advice.
BridgeBio Pharma, Inc., a biopharmaceutical company, discovers develops, and delivers medicines for patients with genetic diseases. The company offers Attruby, a next-generation oral small molecule near-complete TTR stabilizer for the treatment of cardiomyopathy of wild-type or transthyretin-mediated amyloidosis (ATTR-CM).
Its portfolio also includes Fosdenopterin, an intravenous formulation of synthetic cyclic pyranopterin monophosphate for the treatment of molybdenum cofactor deficiency under the NULIBRY brand name, and low-dose infigratinib, an oral FGFR1-3 selective tyrosine kinase inhibitor, which is in Phase 3 clinical stage or the treatment of children with achondroplasia and hypochondroplasia.
It also develops Encaleret, an oral small molecule, negative allosteric modulator of the calcium sensing receptor, which is in phase 3 clinical study for the treatment of Autosomal Dominant Hypocalcemia Type 1(ADH1) and Chronic Hypoparathyroidism (CHP).
Its portfolio also includes BBP-418, an investigational, orally administered, and small molecule therapy that is in phase 3 clinical study for the treatment of LGMD2I, and BBP-812, an investigational adeno-associated virus (AAV) gene therapy for Canavan disease. Additionally, it engages in developing products for mendelian, oncology, and gene therapy diseases.
Founded in 2015, It has license and collaboration agreements with the Bayer Consumer Care AG, Alexion Pharma International Operations Limited Company, Leland Stanford Junior University, and Novartis International Pharmaceutical Ltd. BridgeBio Pharma is headquartered in Palo Alto, California.
BridgeBio Pharma, Inc. is a biopharmaceutical company focused on discovering, developing, and delivering medicines for patients with genetic diseases. Its commercial product is Attruby, a next-generation oral small molecule TTR stabilizer for treating cardiomyopathy of wild-type or transthyretin-mediated amyloidosis (ATTR-CM). The company also markets NULIBRY (fosdenopterin) for molybdenum cofactor deficiency. Its pipeline includes low-dose infigratinib (FGFR1-3 inhibitor) in Phase 3 for achondroplasia and hypochondroplasia, encaleret for Autosomal Dominant Hypocalcemia Type 1 and chronic hypoparathyroidism, BBP-418 for LGMD2I, and BBP-812 (AAV gene therapy) for Canavan disease. BridgeBio also has programs in mendelian, oncology, and gene therapy areas.
Where is BridgeBio Pharma (BBIO) listed and in which currency?
BridgeBio Pharma is listed on the Nasdaq Global Select Market (NasdaqGS) under the ticker symbol BBIO. Its shares trade in United States dollars (USD), which is the company's reporting currency. As a US-based company listed on a major American exchange, its stock is accessible to investors through standard brokerage accounts and is subject to US securities regulations.
What sector and industry does BridgeBio Pharma (BBIO) belong to?
BridgeBio Pharma operates in the Healthcare sector and specifically within the Biotechnology industry. This classification reflects its focus on developing innovative therapies for genetic diseases using advanced biotechnological approaches, including small molecules, enzyme replacement, and gene therapy. As a biotechnology company, it engages in research, clinical development, and commercialization of treatments that target underlying genetic causes of diseases, often addressing rare or underserved conditions.
Where is BridgeBio Pharma headquartered and what markets does it serve?
BridgeBio Pharma is headquartered in the United States. The company's description indicates it serves patients with genetic diseases globally, though its primary market is the US, where it has commercial products like Attruby and NULIBRY. It also has license and collaboration agreements with international partners such as Bayer Consumer Care AG (Switzerland), Alexion Pharma International Operations (Ireland), Leland Stanford Junior University (US), and Novartis International Pharmaceutical Ltd. (Switzerland), suggesting a global reach in research and development.
How does BridgeBio Pharma (BBIO) generate revenue?
BridgeBio Pharma generates revenue primarily through the commercialization of its approved products. Its main commercial product is Attruby, an oral TTR stabilizer for ATTR-CM, and NULIBRY (fosdenopterin) for molybdenum cofactor deficiency. Additionally, the company may earn revenue from license and collaboration agreements, such as those with Bayer, Alexion, Stanford, and Novartis, which could include upfront payments, milestones, and royalties. Its pipeline, if approved, would add future revenue streams from products like infigratinib, encaleret, BBP-418, and BBP-812. The company also invests in research and development to expand its portfolio.