Attruby's Triumph | BridgeBio's flagship drug Attruby exceeds sales expectations, capturing significant market share in ATTR-CM treatment and driving stock performance |
Pipeline Potential | Explore BridgeBio's diverse late-stage pipeline, including promising candidates like encaleret and infigratinib, with potential to address multiple genetic diseases |
Market Dynamics | Delve into BridgeBio's strategic positioning in the competitive ATTR-CM market, leveraging education initiatives and partnerships to expand patient reach |
Financial Outlook | Analyst price targets range from $37 to $95, with a consensus "Strong Buy" recommendation, reflecting optimism despite current unprofitability |
Metrics to compare | BBIO | Sector Sector - Average of metrics from a broad group of related Healthcare sector companies | Relationship RelationshipBBIOPeersSector | |
|---|---|---|---|---|
P/E Ratio | −21.0x | −1.6x | −0.4x | |
PEG Ratio | 3.54 | −0.07 | 0.00 | |
Price/Book | −6.6x | 2.1x | 2.6x | |
Price / LTM Sales | 26.1x | 9.0x | 3.1x | |
Upside (Analyst Target) | 29.6% | 169.9% | 48.8% | |
Fair Value Upside | Unlock | 12.7% | 6.3% | Unlock |
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); 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); 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. In addition, the company engages in developing products for mendelian, oncology, and gene therapy diseases. 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, Inc. was founded in 2015 and is headquartered in Palo Alto, California.