BridgeBio Pharma, Inc. (BBIO)

US — Healthcare Sector
Peers: RVMD  IONS  ASND  SMMT  ROIV  MRNA  BMRN  EXEL  RNA  JAZZ 

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Key Metrics & Ratings

  • symbol BBIO
  • Rev/Share 1.8569
  • Book/Share -10.0922
  • PB -6.693
  • Debt/Equity -0.9621
  • CurrentRatio 3.8753
  • ROIC -0.775

 

  • MktCap 13086868190.0
  • FreeCF/Share -3.1242
  • PFCF -21.9869
  • PE -16.231
  • Debt/Assets 1.863
  • DivYield 0
  • ROE 0.4663

 

  • Rating C
  • Score 2
  • Recommendation Sell
  • P/E Score 1
  • DCF Score 1
  • P/B Score 1
  • D/E Score 1

Recent Analyst Ratings

Type Ticker Analyst Firm Previous Rating Current Rating Previous Price Target Current Price Target Date
Initiation BBIO Barclays -- Overweight -- $157 Jan. 28, 2026
Initiation BBIO Morgan Stanley -- Overweight -- $96 Jan. 6, 2026
Initiation BBIO Bernstein -- Outperform -- $94 Dec. 11, 2025
Resumed BBIO Raymond James -- Outperform -- $56 July 30, 2025
Initiation BBIO Truist -- Buy -- $66 July 21, 2025
Initiation BBIO Jefferies -- Buy -- $70 July 14, 2025
Upgrade BBIO Oppenheimer Perform Outperform -- $60 July 9, 2025
Initiation BBIO Wolfe Research -- Outperform -- $49 June 17, 2025
Initiation BBIO Redburn Atlantic -- Buy -- $50 March 31, 2025
Initiation BBIO Scotiabank -- Sector Outperform -- -- Oct. 16, 2024

News

BridgeBio Pharma (BBIO) Reports Q4 Loss, Tops Revenue Estimates
BBIO
Published: February 20, 2025 by: Zacks Investment Research
Sentiment: Negative

BridgeBio Pharma (BBIO) came out with a quarterly loss of $1.31 per share versus the Zacks Consensus Estimate of a loss of $1.09. This compares to loss of $0.96 per share a year ago.

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image for news BridgeBio Pharma (BBIO) Reports Q4 Loss, Tops Revenue Estimates
BridgeBio Pharma Reports Fourth Quarter and Full Year 2024 Financial Results and Commercial Update
BBIO
Published: February 20, 2025 by: GlobeNewsWire
Sentiment: Neutral

- As of February 17, 2025, 1,028 unique patient prescriptions for Attruby™ have been written by 516 unique prescribers since FDA approval - Attruby (acoramidis), the first and only near-complete TTR stabilizer (≥90%) was approved by the FDA to reduce cardiovascular death and cardiovascular-related hospitalization in ATTR-CM patients on November 22, 2024 - Acoramidis was approved as BEYONTTRA™ in the EU on February 10, 2025, achieving a $75 million milestone payment and ongoing royalties in a tiered structure beginning in the low-thirties percent on sales in the EU - Acoramidis demonstrated a 59% hazard reduction on the composite endpoint of …

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image for news BridgeBio Pharma Reports Fourth Quarter and Full Year 2024 Financial Results and Commercial Update
BridgeBio Pharma to Report Fourth Quarter and Full Year 2024 Financial Results and Business Update on February 20, 2025
BBIO
Published: February 13, 2025 by: GlobeNewsWire
Sentiment: Neutral

PALO ALTO, Calif., Feb. 13, 2025 (GLOBE NEWSWIRE) -- BridgeBio Pharma, Inc. (Nasdaq: BBIO) (“BridgeBio” or the “Company”), a new type of biopharmaceutical company focused on genetic diseases, today announced that it will report financial results for the fourth quarter and full year ended December 31, 2024, on February 20, 2025. As part of the announcement, the Company will also share updates on Attruby's commercialization progress and its late-stage clinical pipeline.

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image for news BridgeBio Pharma to Report Fourth Quarter and Full Year 2024 Financial Results and Business Update on February 20, 2025

About BridgeBio Pharma, Inc. (BBIO)

  • IPO Date 2019-06-27
  • Website https://www.bridgebio.com
  • Industry Biotechnology
  • CEO Neil Kumar
  • Employees 725

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.