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BridgeBio Pharma (BBIO) Stock

Profile

Sector:

Healthcare

Industry:

Biotechnology

Country:

United States

IPO:

27 June 2019

Indexes:

Not included

Description:

BridgeBio Pharma, Inc. is a pharmaceutical company engaged in research and development of various drugs for genetic diseases. The company was founded in 2015, with its headquarters located in Palo Alto, California. BridgeBio Pharma's portfolio includes about 20 development programs for various products at different stages of development. The company's main candidates are: BBP-265, an oral low-molecular-weight transthyretin (TTR) intended for the treatment of transthyretin amyloidosis. Infigratinib, an oral selective FGFR1-3 tyrosine kinase inhibitor for the treatment of FGFR-driven cancer and achondroplasia. BBP-631, a preclinical gene transfer candidate product for the treatment of congenital adrenal hyperplasia (CAH) caused by 21OHD. BBP-454, a preclinical research program focused on new approaches to inhibiting KRAS for cancer treatment.

Events Calendar

Earnings

Next earnings date:

Feb 21, 2025

Recent quarterly earnings:

Nov 12, 2024

Recent annual earnings:

Feb 22, 2024
Dividend

Next ex-dividend date:

N/A

Recent ex-dividend date:

N/A
Splits

Next split:

N/A

Recent split:

N/A

Analyst ratings

Recent major analysts updates

23 Dec '24 Evercore ISI Group
Outperform
16 Dec '24 HC Wainwright & Co.
Buy
25 Nov '24 Scotiabank
Sector Outperform
25 Nov '24 HC Wainwright & Co.
Buy
25 Nov '24 B of A Securities
Buy
15 Nov '24 Scotiabank
Sector Outperform
25 Oct '24 HC Wainwright & Co.
Buy
17 Oct '24 Leerink Partners
Outperform
16 Oct '24 Scotiabank
Sector Outperform
03 Oct '24 Oppenheimer
Perform

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Institutional Ownership

Acoramidis Receives Positive CHMP Opinion for Treatment of Transthyretin Amyloid Cardiomyopathy (ATTR-CM)
Acoramidis Receives Positive CHMP Opinion for Treatment of Transthyretin Amyloid Cardiomyopathy (ATTR-CM)
Acoramidis Receives Positive CHMP Opinion for Treatment of Transthyretin Amyloid Cardiomyopathy (ATTR-CM)
BBIO
globenewswire.com13 December 2024

PALO ALTO, Calif., Dec. 13, 2024 (GLOBE NEWSWIRE) -- BridgeBio Pharma, Inc. (Nasdaq: BBIO) is a biopharmaceutical company that focuses on genetic diseases. Today, they announced that the Committee for Medicinal Products for Human Use (CHMP) has given a positive recommendation for marketing authorization in the European Union (EU) for acoramidis, a treatment for wild-type or variant transthyretin amyloidosis in adults with cardiomyopathy (ATTR-CM). In the Phase 3 study ATTRibute-CM, acoramidis demonstrated significant improvements in cardiovascular outcomes.

Unnatural Products Announces BridgeBio Exercises Option to License Macrocyclic Therapeutics for Development in Rare Diseases and Oncology
Unnatural Products Announces BridgeBio Exercises Option to License Macrocyclic Therapeutics for Development in Rare Diseases and Oncology
Unnatural Products Announces BridgeBio Exercises Option to License Macrocyclic Therapeutics for Development in Rare Diseases and Oncology
BBIO
globenewswire.com03 December 2024

SANTA CRUZ, Calif., Dec. 03, 2024 (GLOBE NEWSWIRE) -- Unnatural Products, Inc. (UNP), a biotech company working on oral macrocyclic peptides for hard-to-target diseases, has announced that BridgeBio Pharma, Inc. (Nasdaq: BBIO) has chosen to license some of the macrocyclic peptide candidates found through UNP's advanced AI-driven chemistry platform.

BridgeBio: Next Chapter Begins After Attruby Approval
BridgeBio: Next Chapter Begins After Attruby Approval
BridgeBio: Next Chapter Begins After Attruby Approval
BBIO
seekingalpha.com24 November 2024

BridgeBio has received FDA approval for Attruby (acoramidis) to treat patients with ATTR-CM. The approval comes with a clear label that contains all important clinical information. Additionally, this approval activates a $500 million milestone payment to BridgeBio from a royalty-backed agreement made earlier this year, alleviating some regulatory and funding concerns for the company.

US FDA approves BridgeBio's drug for rare heart condition
US FDA approves BridgeBio's drug for rare heart condition
US FDA approves BridgeBio's drug for rare heart condition
BBIO
reuters.com22 November 2024

On Friday, BridgeBio announced that the U.S. Food and Drug Administration has approved its medication for a rare and serious heart condition. This makes it the first new treatment available in a market largely controlled by Pfizer's popular drug, Vyndaqel.

Attruby™ (acoramidis), a Near Complete TTR Stabilizer (≥90%), approved by FDA to Reduce Cardiovascular Death and Cardiovascular-related Hospitalization in ATTR-CM Patients
Attruby™ (acoramidis), a Near Complete TTR Stabilizer (≥90%), approved by FDA to Reduce Cardiovascular Death and Cardiovascular-related Hospitalization in ATTR-CM Patients
Attruby™ (acoramidis), a Near Complete TTR Stabilizer (≥90%), approved by FDA to Reduce Cardiovascular Death and Cardiovascular-related Hospitalization in ATTR-CM Patients
BBIO
globenewswire.com22 November 2024

Attruby is the first and only approved treatment that clearly states it can nearly fully stabilize TTR. It has been proven to maintain the natural role of TTR in transporting thyroxine and vitamin A, and it also shows positive effects on heart health.

BridgeBio Pharma Announces Publication in the New England Journal of Medicine of Phase 2 PROPEL 2 Study of Infigratinib for Children Living with Achondroplasia
BridgeBio Pharma Announces Publication in the New England Journal of Medicine of Phase 2 PROPEL 2 Study of Infigratinib for Children Living with Achondroplasia
BridgeBio Pharma Announces Publication in the New England Journal of Medicine of Phase 2 PROPEL 2 Study of Infigratinib for Children Living with Achondroplasia
BBIO
globenewswire.com18 November 2024

In Cohort 5 of PROPEL 2, taking infigratinib daily at a dose of 0.25mg/kg led to significant and lasting improvements in annualized height velocity (AHV). At Month 18, the average increase from the starting point was +2.50cm per year, with a p-value of 0.001.

BridgeBio Announces Publication of Case Study Exploring Portfolio Theory's Impact on Biomedical Innovation in The Journal of Portfolio Management
BridgeBio Announces Publication of Case Study Exploring Portfolio Theory's Impact on Biomedical Innovation in The Journal of Portfolio Management
BridgeBio Announces Publication of Case Study Exploring Portfolio Theory's Impact on Biomedical Innovation in The Journal of Portfolio Management
BBIO
globenewswire.com05 November 2024

A case study was written by both senior management at BridgeBio and Andrew W. Lo, Ph.D., who is a co-founder of BridgeBio and a professor at MIT.

3 Top Stocks That Could Still Rocket Higher in 2024
3 Top Stocks That Could Still Rocket Higher in 2024
3 Top Stocks That Could Still Rocket Higher in 2024
BBIO
fool.com04 October 2024

Future decisions from the Food and Drug Administration could significantly increase the value of these stocks.

BridgeBio to Present Outcomes Data Through 42 Months from the Open-Label Extension of ATTRibute-CM, the Phase 3 Study of Acoramidis for Treatment of ATTR-CM, at 2024 AHA Scientific Sessions
BridgeBio to Present Outcomes Data Through 42 Months from the Open-Label Extension of ATTRibute-CM, the Phase 3 Study of Acoramidis for Treatment of ATTR-CM, at 2024 AHA Scientific Sessions
BridgeBio to Present Outcomes Data Through 42 Months from the Open-Label Extension of ATTRibute-CM, the Phase 3 Study of Acoramidis for Treatment of ATTR-CM, at 2024 AHA Scientific Sessions
BBIO
globenewswire.com03 October 2024

PALO ALTO, Calif., Oct. 03, 2024 (GLOBE NEWSWIRE) -- BridgeBio Pharma, Inc. (Nasdaq: BBIO), a biopharmaceutical company that focuses on genetic diseases, announced that it will present data from its ongoing long-term study of acoramidis in ATTR-CM at the American Heart Association (AHA) Scientific Sessions in Chicago from November 16 to 18, 2024. This presentation will include outcomes data collected over 42 months from the Phase 3 ATTRibute-CM study. Additionally, BridgeBio will showcase three posters during moderated sessions on ATTR-CM.

BridgeBio Shares Recurrent Event Analysis of ATTRibute-CM, Demonstrating a 42% Reduction by Acoramidis on the Composite Endpoint of All-Cause Mortality and Recurrent Cardiovascular-related Hospitalization Events
BridgeBio Shares Recurrent Event Analysis of ATTRibute-CM, Demonstrating a 42% Reduction by Acoramidis on the Composite Endpoint of All-Cause Mortality and Recurrent Cardiovascular-related Hospitalization Events
BridgeBio Shares Recurrent Event Analysis of ATTRibute-CM, Demonstrating a 42% Reduction by Acoramidis on the Composite Endpoint of All-Cause Mortality and Recurrent Cardiovascular-related Hospitalization Events
BBIO
globenewswire.com27 September 2024

The Acoramidis treatment resulted in a significant decrease in overall deaths and repeat hospital visits for heart-related issues after 30 months when compared to the placebo group.

FAQ

  • What is the primary business of BridgeBio Pharma?
  • What is the ticker symbol for BridgeBio Pharma?
  • Does BridgeBio Pharma pay dividends?
  • What sector is BridgeBio Pharma in?
  • What industry is BridgeBio Pharma in?
  • What country is BridgeBio Pharma based in?
  • When did BridgeBio Pharma go public?
  • Is BridgeBio Pharma in the S&P 500?
  • Is BridgeBio Pharma in the NASDAQ 100?
  • Is BridgeBio Pharma in the Dow Jones?
  • When was BridgeBio Pharma's last earnings report?
  • When does BridgeBio Pharma report earnings?
  • Should I buy BridgeBio Pharma stock now?

What is the primary business of BridgeBio Pharma?

BridgeBio Pharma, Inc. is a pharmaceutical company engaged in research and development of various drugs for genetic diseases. The company was founded in 2015, with its headquarters located in Palo Alto, California. BridgeBio Pharma's portfolio includes about 20 development programs for various products at different stages of development. The company's main candidates are: BBP-265, an oral low-molecular-weight transthyretin (TTR) intended for the treatment of transthyretin amyloidosis. Infigratinib, an oral selective FGFR1-3 tyrosine kinase inhibitor for the treatment of FGFR-driven cancer and achondroplasia. BBP-631, a preclinical gene transfer candidate product for the treatment of congenital adrenal hyperplasia (CAH) caused by 21OHD. BBP-454, a preclinical research program focused on new approaches to inhibiting KRAS for cancer treatment.

What is the ticker symbol for BridgeBio Pharma?

The ticker symbol for BridgeBio Pharma is NASDAQ:BBIO

Does BridgeBio Pharma pay dividends?

No, BridgeBio Pharma does not pay dividends

What sector is BridgeBio Pharma in?

BridgeBio Pharma is in the Healthcare sector

What industry is BridgeBio Pharma in?

BridgeBio Pharma is in the Biotechnology industry

What country is BridgeBio Pharma based in?

BridgeBio Pharma is headquartered in United States

When did BridgeBio Pharma go public?

BridgeBio Pharma's initial public offering (IPO) was on 27 June 2019

Is BridgeBio Pharma in the S&P 500?

No, BridgeBio Pharma is not included in the S&P 500 index

Is BridgeBio Pharma in the NASDAQ 100?

No, BridgeBio Pharma is not included in the NASDAQ 100 index

Is BridgeBio Pharma in the Dow Jones?

No, BridgeBio Pharma is not included in the Dow Jones index

When was BridgeBio Pharma's last earnings report?

BridgeBio Pharma's most recent earnings report was on 12 November 2024

When does BridgeBio Pharma report earnings?

The next expected earnings date for BridgeBio Pharma is 21 February 2025

Should I buy BridgeBio Pharma stock now?

As of today, analysts generally recommend a 'Buy' rating. However, it's important to do your own research and consider your financial situation before making any investment decisions