BridgeBio Pharma, Inc. - Common Stock (BBIO)
33.54
+0.53 (1.61%)
Bridgebio Pharma is a biotechnology company focused on developing innovative therapies for genetic diseases and cancers
The company employs a collaborative approach, partnering with academic institutions and other organizations to advance its research and development efforts. Bridgebio aims to address significant unmet medical needs by leveraging its expertise in drug discovery and clinical development, with a portfolio that includes targeted therapies and programs designed to tackle fundamental genetic abnormalities. Through its commitment to scientific innovation, Bridgebio strives to improve patient outcomes and contribute to the future of precision medicine.
Previous Close | 33.01 |
---|---|
Open | 32.72 |
Bid | 32.04 |
Ask | 34.44 |
Day's Range | 31.69 - 33.92 |
52 Week Range | 21.62 - 39.47 |
Volume | 2,988,966 |
Market Cap | 5.38B |
PE Ratio (TTM) | -11.69 |
EPS (TTM) | -2.9 |
Dividend & Yield | N/A (N/A) |
1 Month Average Volume | 3,427,385 |
News & Press Releases

Via The Motley Fool · March 3, 2025

Via Benzinga · February 27, 2025

PALO ALTO, Calif., Feb. 25, 2025 (GLOBE NEWSWIRE) -- BridgeBio Pharma, Inc. (Nasdaq: BBIO) (the “Company,” “we” or “BridgeBio”) announced today the pricing of $500 million aggregate principal amount of 1.75% convertible senior notes due 2031 (the “notes”) in a private offering (the “offering”) to qualified institutional buyers pursuant to Rule 144A under the Securities Act of 1933, as amended (the “Securities Act”). In connection with the offering, the Company granted the initial purchasers an option to purchase up to an additional $75 million aggregate principal amount of notes. The sale of the notes is expected to close on February 28, 2025, subject to customary closing conditions.
By BridgeBio Pharma, Inc. · Via GlobeNewswire · February 26, 2025

- Long term debt management strategy will strengthen the balance sheet without increasing total liabilities
By BridgeBio Pharma, Inc. · Via GlobeNewswire · February 24, 2025

- As of February 17, 2025, 1,028 unique patient prescriptions for Attruby™ have been written by 516 unique prescribers since FDA approval
By BridgeBio Pharma, Inc. · Via GlobeNewswire · February 20, 2025

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.
By BridgeBio Pharma, Inc. · Via GlobeNewswire · February 13, 2025

PALO ALTO, Calif., Feb. 11, 2025 (GLOBE NEWSWIRE) -- BridgeBio Pharma, Inc. (Nasdaq: BBIO) (“BridgeBio” or the “Company”), a new type of biopharmaceutical company focused on genetic diseases, today announced the European Commission has granted marketing authorization in the European Union (EU) for acoramidis, under the brand name BEYONTTRA™, for the treatment of wild-type or variant transthyretin amyloidosis in adult patients with cardiomyopathy (ATTR-CM). Acoramidis is a selective small molecule, orally administered near-complete (≥90%) transthyretin (TTR) stabilizer. ATTR-CM is a progressive fatal disease that presents as an infiltrative, restrictive cardiomyopathy resulting in heart failure. Bayer will be responsible for all commercial activity for acoramidis in the EU.
By BridgeBio Pharma, Inc. · Via GlobeNewswire · February 11, 2025

Many stocks flashed buy signals as the major indexes rose to or above key levels.
Via Investor's Business Daily · January 17, 2025

BridgeBio Pharma stock saw a positive improvement to its Relative Strength (RS) Rating on Tuesday, with an increase from 64 to 87.
Via Investor's Business Daily · January 14, 2025

Some companies saw their shares skyrocket on preliminary reports, but others took hits.
Via Investor's Business Daily · January 13, 2025

- Remarkable early Attruby demand: 430 scripts written by 248 unique HCPs since FDA approval with broad uptake across academic centers and community centers in all patient types
By BridgeBio Pharma, Inc. · Via GlobeNewswire · January 13, 2025

Biotech stocks have seen three years of sideways to down trading. But obesity drugs, AI and Trump 2.0 promise to shake things up.
Via Investor's Business Daily · January 9, 2025

PALO ALTO, Calif., Jan. 08, 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 co-founder and CEO, Neil Kumar, Ph.D., will present at the 43rd Annual J.P. Morgan Healthcare Conference in San Francisco, CA on Monday, January 13 at 7:30 am PT.
By BridgeBio Pharma, Inc. · Via GlobeNewswire · January 8, 2025

PALO ALTO, Calif., Dec. 13, 2024 (GLOBE NEWSWIRE) -- BridgeBio Pharma, Inc. (Nasdaq: BBIO) (“BridgeBio” or the “Company”), a new type of biopharmaceutical company focused on genetic diseases, announced today that the Committee for Medicinal Products for Human Use (CHMP) has adopted a positive opinion recommending marketing authorization in the European Union (EU) for acoramidis for the treatment of wild-type or variant transthyretin amyloidosis in adult patients with cardiomyopathy (ATTR-CM). Acoramidis is a selective small molecule, orally administered near-complete (≥90%) transthyretin (TTR) stabilizer. ATTR-CM is a progressive fatal disease that presents as an infiltrative, restrictive cardiomyopathy resulting in heart failure. In the Phase 3 study ATTRibute-CM, acoramidis showed clear benefits on cardiovascular outcomes.
By BridgeBio Pharma, Inc. · Via GlobeNewswire · December 13, 2024

BridgeBio will sell its drug at a slightly lower wholesale acquisition cost compared to Pfizer's blockbuster, Vyndaqel.
Via Investor's Business Daily · November 25, 2024

Via Benzinga · November 25, 2024

Via Benzinga · November 25, 2024

Via Benzinga · November 25, 2024

Via Benzinga · November 25, 2024

FDA approves BridgeBio's Attruby for ATTR-CM. Phase 3 results highlight its effectiveness in reducing cardiovascular risks and improving life quality.
Via Benzinga · November 25, 2024

- Attruby is the first and only approved product with a label specifying near-complete stabilization of TTR. Attruby has been shown to preserve the native function of TTR as a transport protein of thyroxine and vitamin A and to demonstrate benefit on cardiovascular outcomes
By BridgeBio Pharma, Inc. · Via GlobeNewswire · November 22, 2024

BridgeBio's acoramidis shows significant reductions in mortality and hospitalizations in ATTR-CM patients, with no new safety concerns in long-term studies.
Via Benzinga · November 19, 2024

- Acoramidis demonstrated the earliest known time to separation in cardiovascular outcomes in the ATTRibute-CM study (3 months), with statistically significant risk reduction of 36% on All-Cause Mortality (ACM) alone at Month 36 within the Open Label Extension
By BridgeBio Pharma, Inc. · Via GlobeNewswire · November 18, 2024