- $353.2 million in total third quarter revenues, primarily comprised of $253.2 million of U.S. Attruby net product revenue (up approximately $31 million sequentially and $145 million year over year). Loss from operations was $11.6 million, driven by increased revenue and a one-time $75.0 million BEYONTTRA sales milestone from Bayer. Cash, cash equivalents and marketable securities were $1.5 billion as of September 30, 2026, fully funding all three launches and expansion indications
- Attruby growth was again led by the treatment-naïve segment, with both the number of newly diagnosed patients starting treatment and Attruby's share of those starts increasing
- Real-world evidence continues to differentiate acoramidis from tafamidis on outcomes that matter to patients, physicians, and payers: (i) an independent Epic COSMOS analysis of 2,684 patients found an 18% lower risk of death, hospitalization, new atrial fibrillation or diuretic escalation (p600 genetically confirmed patients identified, up from approximately 500 last quarter, and the U.S. field team is fully deployed
- The first participant was dosed in RECLAIM-HP, the Phase 3 study for encaleret in chronic hypoparathyroidism. Topline data are expected in early 2028, representing a potential second indication in an estimated population of 200,000 patients in the U.S. and EU
PALO ALTO, Calif., Oct. 29, 2026
(GLOBE NEWSWIRE)
-- BridgeBio Pharma, Inc. (Nasdaq: BBIO) (“BridgeBio” or the “Company”), a commercial-stage, multi-product biopharmaceutical company focused on developing medicines for genetic conditions, announced today its financial results for the third quarter ended September 30, 2026, and provided an update on Attruby’s commercial progress.
Pipeline Overview:
Program
Status
Next expected milestone
Acoramidis for ATTR-CM
Approved in U.S., EU, Japan, Switzerland, Brazil, U.K., and Australia
New data to be shared at AHA 2026
BBP-418 for LGMD2I/R9
PDUFA date set for November 27, 2026, with Priority Review
U.S. launch upon FDA approval
Oral infigratinib for achondroplasia
PDUFA date set for February 4, 2027, with Priority Review; MAA submitted to EMA
U.S. launch upon FDA approval
Encaleret for ADH1
PDUFA date set for May 8, 2027, with Priority Review; MAA submitted to EMA
U.S. launch upon FDA approval
Encaleret for chronic hypoparathyroidism
First participant dosed in RECLAIM-HP, registrational Phase 3 study
Topline data anticipated early 2028
Oral infigratinib for hypochondroplasia
Enrolling additional dose cohorts for Phase 2 study
Initiation of dosing in additional dose cohorts
Depleter (BBP-717) for ATTR-CM
Development candidate nomination
Submit IND to the FDA in 2027
“I’m heartened by how consistently the evidence for acoramidis keeps pointing in the same direction,” said Neil Kumar, Chief Executive Officer of BridgeBio. “This quarter we added two more large real-world comparisons to a growing body of data showing acoramidis outperforming tafamidis on the outcomes that matter most to patients: survival and hospitalizations. This is exactly what you would expect from the only near-complete stabilizer on the market, and it is deeply gratifying to see it borne out in the real world. This is also a particularly special moment for the company. Three PDUFA dates fall within the next seven months, each with the potential to be a first for communities that have waited far too long: BBP-418 for LGMD2I/R9, where no approved therapy exists; infigratinib as the first oral option for achondroplasia; and encaleret for ADH1, which has never had a therapy of its own.”
Commercial Updates:
The third quarter total revenues, net totaled $353.2 million, comprised of $253.2 million of U.S. Attruby net product revenue, $0.1 million of Rest of World Attruby net product revenue, $20.5 million from royalty revenue, and $79.3 million in license and services revenue.
“Attruby delivered another quarter of sequential growth, driven by continued gains in first-line share, and the real-world evidence emerging across independent datasets continues to reinforce its position as the stabilizer of choice,” said Matt Outten, Chief Commercial Officer of BridgeBio. “This is a pivotal moment for BridgeBio as we stand weeks away from the potential approval of BBP-418, the first and only treatment for LGMD2I/R9, followed by infigratinib in February and encaleret in May. Our field teams for all three programs are hired and ready to serve these communities from day one.”
Pipeline Updates:
Attruby (acoramidis) – First and only near-complete (≥90%) transthyretin (TTR) stabilizer for treatment of transthyretin amyloid cardiomyopathy (ATTR-CM):
Acoramidis significantly reduced the risk of early clinical worsening versus tafamidis in the first peer-reviewed, contemporary real-world comparative effectiveness study of TTR stabilizers, published in Cardiology and Therapy
1
using U.S. claims data, with a statistically and clinically significant 34% reduction in composite clinical worsening (HR 0.66; p=0.046) and a 43% reduction in diuretic intensification (HR 0.57; p=0.021). Separation in clinical outcomes emerged within weeks of treatment initiation and increased over time.
BridgeBio presented
2
an independent, real-world, propensity score-matched analysis of 2,684 individuals with ATTR-CM from a contemporary population in the Epic COSMOS U.S. electronic health record database at the Heart Failure Society of America Annual Scientific Meeting 2026. Compared with tafamidis, acoramidis was associated with an 18% lower risk of a composite of death, all-cause hospitalization, new-onset atrial fibrillation, and diuretic intensification (HR 0.82; p600 genetically confirmed patients identified, up from approximately 500 last quarter.
CALIBRATE-PEDS, the registrational Phase 2/3 study of encaleret in pediatric ADH1, is ongoing and has completed enrollment in the first of four cohorts (adolescents 12 to 17 years of age).
The first participant was dosed in RECLAIM-HP, the registrational Phase 3 study of encaleret in chronic hypoparathyroidism. Topline results from the study are anticipated in early 2028. Chronic hypoparathyroidism affects approximately 200,000 patients in the U.S. and EU and represents a substantial expansion of the encaleret opportunity beyond ADH1. Encaleret is the only oral therapy in development being evaluated to normalize both blood and urine calcium in this population.
BBP-717 – Monoclonal antibody depleter for ATTR-CM:
BridgeBio nominated BBP-717 as a development candidate. BBP-717 is a next-generation monoclonal antibody designed to deplete amyloid deposits in patients with ATTR-CM. The Company plans to submit an Investigational New Drug (IND) application to the FDA in 2027.
BBP-717 builds on BridgeBio’s leadership in ATTR-CM and is designed to complement near-complete TTR stabilization by clearing existing amyloid deposits.
Financial Updates:
Cash, Cash Equivalents and Marketable Securities
Cash, cash equivalents and marketable securities totaled $1.5 billion and $587.5 million as of September 30, 2026 and December 31, 2025, respectively.
Total Revenues, Net
Three Months Ended September 30,
Nine Months Ended September 30,
2026
2025
2026
2025
(in thousands)
Net product revenue
$
253,346
$
108,111
$
656,382
$
216,351
License and services revenue
79,314
8,311
89,537
125,441
Royalty revenue
20,511
4,278
45,443
6,106
Total revenues, net
$
353,171
$
120,700
$
791,362
$
347,898
Total revenues, net for the three months ended September 30, 2026 were $353.2 million compared to $120.7 million for the same period in 2025. The $232.5 million increase was primarily driven by a $145.2 million increase in Attruby net product revenue, a $71.1 million increase in license and services revenue primarily due to recognition of a $75.0 million sales milestone under the Bayer License Agreement achieved during the third quarter of 2026, and a $16.2 million increase in royalty revenue primarily earned from net product sales of BEYONTTRA in the EU and Japan.
Total revenues, net for the nine months ended September 30, 2026 were $791.4 million compared to $347.9 million for the same period in 2025. The $443.5 million increase was primarily driven by a $440.0 million increase in Attruby net product revenue and a $39.3 million increase in royalty revenue primarily earned from net product sales of BEYONTTRA in the EU and Japan. These increases were partially offset by a $35.8 million decrease in license and services revenue. This decrease was primarily due to recognition of $105.0 million of regulatory milestone-related revenues during the nine months ended September 30, 2025, partially offset by recognition of a $75.0 million sales milestone under the Bayer License Agreement achieved during the third quarter of 2026.
Total Operating Costs and Expenses
Three Months Ended September 30,
Nine Months Ended September 30,
2026
2025
2026
2025
(in thousands)
Total cost of revenues
$
20,450
$
6,563
$
45,435
$
12,855
Research and development
143,506
112,874
419,590
335,536
Selling, general and administrative
200,854
137,621
551,011
373,140
Restructuring, impairment, and related charges
—
8,841
—
10,216
Total operating costs and expenses
$
364,810
$
265,899
$
1,016,036
$
731,747
Total operating costs and expenses for the three months ended September 30, 2026 were $364.8 million, compared to $265.9 million for the same period in 2025. The $98.9 million increase was primarily driven by a $63.2 million increase in selling, general and administrative (SG&A) expenses, reflecting continued investment in both the ongoing commercialization of Attruby and the pre-commercial activities for BridgeBio's late-stage product candidates, a $30.6 million increase in research and development (R&D) expenses to support the development of late-stage product candidates, and a $13.9 million increase in total cost of revenues primarily due to higher sales volume of Attruby.
Total operating costs and expenses for the nine months ended September 30, 2026 were $1.0 billion, compared to $731.7 million for the same period in 2025. The $284.3 million increase was primarily driven by a $177.9 million increase in SG&A expenses, reflecting continued investment in both the ongoing commercialization of Attruby and the pre-commercial activities for BridgeBio's late-stage product candidates, an $84.1 million increase in R&D expenses to support the development of late-stage product candidates, and a $32.6 million increase in total cost of revenues primarily due to higher sales volume of Attruby.
Stock-based compensation expenses included in operating costs and expenses for the three months ended September 30, 2026 were $39.9 million, of which $24.6 million, $14.9 million, and $0.4 million were included in SG&A expenses, R&D expenses, and cost of goods sold, respectively. Stock-based compensation expenses included in operating costs and expenses for the same period in 2025 were $35.3 million, of which $21.9 million, $12.3 million, $0.7 million, and $0.4 million were included in SG&A expenses, R&D expenses, restructuring, impairment, and related charges, and cost of goods sold, respectively.
Stock-based compensation expenses included in operating costs and expenses for the nine months ended September 30, 2026 were $117.7 million, of which $73.2 million, $42.5 million, and $2.0 million were included in SG&A expenses, R&D expenses, and cost of goods sold, respectively. Stock-based compensation expenses included in operating costs and expenses for the same period in 2025 were $102.0 million, of which $63.1 million, $37.6 million, $0.7 million, and $0.6 million were included in SG&A expenses, R&D expenses, restructuring, impairment, and related charges, and cost of goods sold, respectively.
Total Other Income (Expense), Net
Total other income (expense), net for the three and nine months ended September 30, 2026, was $(47.6) million and $(157.0) million, respectively, compared to $(41.3) million and $(153.9) million, respectively, for the same periods in 2025.
The increase in total other income (expense), net of $6.3 million for the three months ended September 30, 2026, compared to the same period in 2025 was primarily driven by a $7.8 million decrease in nonrecurring noncash income from an equity method investment recognized in 2025, a $5.9 million increase in noncash interest expense related to deferred royalty obligations, and a $4.2 million decrease in other income resulting from changes in the valuation of the embedded derivative liability component of our deferred royalty obligation. These changes were partially offset by an $8.5 million decrease in net loss from equity method investments and a $6.9 million increase in interest income.
The increase in total other income (expense), net of $3.1 million for the nine months ended September 30, 2026, compared to the same period in 2025 was primarily driven by a $37.0 million increase in noncash interest expense related to deferred royalty obligations, a $7.8 million decrease in nonrecurring noncash income from an equity method investment recognized in 2025, a $4.9 million decrease in net gains on foreign currency transactions, and a $4.0 million decrease in other income resulting from changes in the valuation of the embedded derivative liability component of our deferred royalty obligation. These changes were partially offset by a $21.2 million decrease in loss on extinguishment of debt recognized in the first quarter of 2025, a $19.5 million decrease in net loss from equity method investments, and a $10.5 million increase in interest income.
Net Loss Attributable to Common Stockholders of BridgeBio and Net Loss per Share
For the three and nine months ended September 30, 2026, the Company recorded a net loss attributable to common stockholders of BridgeBio of $83.0 million and $399.3 million, respectively, compared to $182.7 million and $532.1 million, respectively, for the same periods in 2025.
For the three and nine months ended September 30, 2026, the Company reported a net loss per share of $0.42 and $2.04, respectively, compared to $0.95 and $2.79, respectively, for the same periods in 2025.
BRIDGEBIO PHARMA, INC.
Condensed Consolidated Statements of Operations
(in thousands, except share and per share amounts)
Three Months Ended September 30,
Nine Months Ended September 30,
2026
2025
2026
2025
(Unaudited)
(Unaudited)
Revenues:
Net product revenue
$
253,346
$
108,111
$
656,382
$
216,351
License and services revenue
79,314
8,311
89,537
125,441
Royalty revenue
20,511
4,278
45,443
6,106
Total revenues, net
353,171
120,700
791,362
347,898
Operating costs and expenses:
Cost of revenues:
Cost of goods sold
12,317
4,028
30,577
8,910
Cost of license, services, and royalty revenue
8,133
2,535
14,858
3,945
Total cost of revenues
20,450
6,563
45,435
12,855
Research and development
143,506
112,874
419,590
335,536
Selling, general and administrative
200,854
137,621
551,011
373,140
Restructuring, impairment, and related charges
—
8,841
—
10,216
Total operating costs and expenses
364,810
265,899
1,016,036
731,747
Loss from operations
(11,639
)
(145,199
)
(224,674
)
(383,849
)
Other income (expense), net:
Interest income
13,105
6,239
26,010
15,522
Interest expense
(13,255
)
(11,739
)
(39,475
)
(41,467
)
Noncash interest expense on deferred royalty obligations
(42,282
)
(36,410
)
(123,500
)
(86,460
)
Net loss from equity method investments
(7,312
)
(15,834
)
(32,030
)
(51,579
)
Loss on extinguishment of debt
—
—
—
(21,155
)
Other income, net
2,116
16,461
11,956
31,240
Total other expense, net
(47,628
)
(41,283
)
(157,039
)
(153,899
)
Loss before income taxes
(59,267
)
(186,482
)
(381,713
)
(537,748
)
Provision for (benefit from) income taxes
1,229
(1,545
)
1,229
555
Net loss
(60,496
)
(184,937
)
(382,942
)
(538,303
)
Net loss attributable to redeemable convertible noncontrolling interests and noncontrolling interests
3,786
2,194
9,973
6,235
Net loss attributable to BridgeBio
(56,710
)
(182,743
)
(372,969
)
(532,068
)
Preferred stock dividends and accretion
26,293
—
26,293
—
Net loss attributable to common stockholders of BridgeBio
$
(83,003
)
$
(182,743
)
$
(399,262
)
$
(532,068
)
Net loss per share attributable to common stockholders of BridgeBio, basic and diluted
$
(0.42
)
$
(0.95
)
$
(2.04
)
$
(2.79
)
Weighted-average shares used in computing net loss per share attributable to common stockholders of BridgeBio, basic and diluted
196,029,851
191,854,152
195,539,752
190,845,133
Three Months Ended September 30,
Nine Months Ended September 30,
Stock-based Compensation
2026
2025
2026
2025
(Unaudited)
(Unaudited)
Cost of goods sold
$
374
$
361
$
2,029
$
578
Research and development
14,921
12,328
42,504
37,582
Selling, general and administrative
24,562
21,866
73,209
63,077
Restructuring, impairment and related charges
—
709
—
755
Total stock-based compensation
$
39,857
$
35,264
$
117,742
$
101,992
BRIDGEBIO PHARMA, INC.
Condensed Consolidated Balance Sheets
(In thousands)
September 30,
2026
December 31,
2025
(Unaudited)
(1)
Assets
Cash, cash equivalents and marketable securities
$
1,538,855
$
587,482
Accounts receivable, net
375,089
139,444
Inventories
59,718
26,753
Prepaid expenses and other current assets
70,944
44,070
Total current assets
2,044,606
797,749
Equity method investments
47,783
79,972
Property and equipment, net
5,042
5,366
Operating lease right-of-use assets
15,746
8,149
Intangible assets, net
25,923
28,077
Other assets
22,686
16,712
Total assets
$
2,161,786
$
936,025
Liabilities, Redeemable Convertible Noncontrolling Interests and Stockholders' Deficit
Accounts payable
$
88,258
$
36,228
Operating lease liabilities, current portion
1,987
6,192
Deferred revenue, current portion
4,744
7,190
2027 Notes, net
548,430
—
Accrued and other current liabilities
333,818
238,361
Total current liabilities
977,237
287,971
Operating lease liabilities, net of current portion
14,645
3,811
Deferred revenue, net of current portion
8,968
13,080
2027 Notes, net
—
547,015
2029 Notes, net
742,437
740,890
2031 Notes, net
566,013
564,565
2033 Notes, net
620,533
—
Deferred royalty obligations, net
884,053
855,030
Other long-term liabilities
1,405
244
Redeemable convertible noncontrolling interests
(1,363
)
(570
)
Series A preferred stock
942,478
—
Common stock
207
202
Treasury stock, at cost
(580,775
)
(323,276
)
Additional paid-in capital
2,170,006
2,057,646
Accumulated other comprehensive income (loss)
(95
)
12
Accumulated deficit
(4,194,163
)
(3,821,194
)
Noncontrolling interests
10,200
10,599
Total liabilities, redeemable convertible noncontrolling interests and stockholders' deficit
$
2,161,786
$
936,025
BRIDGEBIO PHARMA, INC.
Condensed Consolidated Statements of Cash Flows
(In thousands)
Nine Months Ended September 30,
2026
2025
(Unaudited)
Operating activities:
Net loss
$
(382,942
)
$
(538,303
)
Adjustments to reconcile net loss to net cash used in operating activities:
Noncash interest expense on deferred royalty obligations
123,500
86,460
Stock-based compensation
117,171
98,385
Net loss from equity method investments
32,030
51,579
Change in fair value of the embedded derivative associated with the deferred royalty obligation
(7,098
)
(11,062
)
Amortization of debt discount and issuance costs
5,670
4,515
Depreciation and amortization
3,308
3,999
Noncash lease expense
4,714
3,443
Loss on extinguishment of debt
—
21,155
Noncash income from an equity method investment
—
(7,769
)
Other noncash adjustments, net
2,233
(1,217
)
Changes in operating assets and liabilities:
Accounts receivable, net
(235,646
)
(111,796
)
Inventories
(35,641
)
(23,356
)
Prepaid expenses and other current assets
(26,872
)
(17,527
)
Other assets
(5,849
)
568
Accounts payable
51,993
9,084
Accrued compensation and benefits
(9,049
)
3,212
Accrued research and development liabilities
13,583
347
Operating lease liabilities
(5,494
)
(4,757
)
Deferred revenue
(6,558
)
(9,480
)
Other liabilities
48,397
53,030
Net cash used in operating activities
(312,550
)
(389,490
)
Investing activities:
Purchases of marketable securities
(63,937
)
(10,876
)
Maturities of marketable securities
76,500
8,000
Proceeds from special cash dividends received from an investment in equity securities
—
2,302
Payment for intangible assets
—
(8,495
)
Purchases of property and equipment
(802
)
(1,064
)
Net cash provided by (used in) investing activities
11,761
(10,133
)
Financing activities:
Proceeds from issuance of 2033 Notes
632,500
—
Issuance costs and discounts associated with 2033 Notes
(13,227
)
—
Proceeds from issuance of 2031 Notes
—
575,000
Issuance costs and discounts associated with 2031 Notes
—
(12,034
)
Repayment of term loans
—
(459,000
)
Proceeds from royalty obligation under Royalty Purchase Agreement (as described in Note 9)
—
300,000
Issuance costs associated with royalty obligation under Royalty Purchase Agreement
—
(3,010
)
Repayments of deferred royalty obligations
(62,507
)
(6,896
)
Proceeds from issuance of preferred stock
933,900
—
Issuance costs associated with preferred stock
(1,342
)
—
Payment of preferred stock dividends
(2,694
)
—
Repurchase of common stock
(252,502
)
(48,276
)
Proceeds from stock option exercises, net of repurchases
33,712
14,523
Proceeds from common stock issuances under ESPP
9,728
6,414
Repurchase of RSU shares to satisfy tax withholding
(13,431
)
(6,796
)
Transactions with noncontrolling interests
—
1,550
Net cash provided by financing activities
1,264,137
361,475
Net increase (decrease) in cash, cash equivalents, and restricted cash
963,348
(38,148
)
Cash, cash equivalents, and restricted cash at beginning of period
572,140
683,244
Cash, cash equivalents, and restricted cash at end of period
$
1,535,488
$
645,096
Nine Months Ended September 30,
2026
2025
(Unaudited)
Supplemental Disclosure of Cash Flow Information:
Cash paid for interest
$
43,135
$
43,670
Supplemental Disclosures of Noncash Investing and Financing Information:
Accretion of preferred stock
$
9,920
$
—
Accrued cash dividends on preferred stock
$
13,679
$
—
Accrual for repurchase of common stock
$
4,997
$
—
Transfers to noncontrolling interests
$
(8,765
)
$
(4,734
)
Reconciliation of Cash, Cash Equivalents and Restricted Cash:
Cash and cash equivalents
$
1,533,363
$
642,951
Restricted cash — Included in “Prepaid expenses and other current assets”
550
126
Restricted cash — Included in “Other assets”
1,575
2,019
Total cash, cash equivalents and restricted cash at end of periods shown on the condensed consolidated statements of cash flows
$
1,535,488
$
645,096
Webcast Information
BridgeBio will host a conference call and webcast to discuss third quarter financial results today, October 29, 2026, at 4:30 pm ET. This event can be accessed at
or by visiting the “Events & Presentations” page within the Investors section of the BridgeBio website at investor.bridgebio.com. A replay of the webcast will be available on the BridgeBio website for 30 days following the event.
About Attruby
®
(acoramidis)
INDICATION
Attruby is a transthyretin stabilizer indicated for the treatment of the cardiomyopathy of wild-type or variant transthyretin-mediated amyloidosis (ATTR-CM) in adults to reduce cardiovascular death and cardiovascular-related hospitalization.
IMPORTANT SAFETY INFORMATION
Adverse Reactions
Diarrhea (11.6% vs 7.6%) and upper abdominal pain (5.5% vs 1.4%) were reported in patients treated with Attruby versus placebo, respectively. The majority of these adverse reactions were mild and resolved without drug discontinuation. Discontinuation rates due to adverse events were similar between patients treated with Attruby versus placebo (9.3% and 8.5%, respectively).
About BridgeBio Pharma, Inc.
BridgeBio exists to develop transformative medicines for genetic conditions. Millions of people worldwide living with genetic conditions lack treatment options, often because drug development for small patient populations can be commercially challenging. We aim to bridge the gap between advancements in genetic science and meaningful medicines for underserved patient populations. Our decentralized, hub-and-spoke model is designed for speed, precision, and scalability. Autonomous and empowered teams focus on individual conditions, while a central hub provides the clinical, regulatory, and commercial capabilities needed to bring innovation to market. For more information, visit
bridgebio.com
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BridgeBio Pharma, Inc. Forward-Looking Statements
This press release contains forward-looking statements. Statements in this press release may include statements that are not historical facts and are considered forward-looking within the meaning of Section 27A of the Securities Act of 1933, as amended (the Securities Act), and Section 21E of the Securities Exchange Act of 1934, as amended (the Exchange Act), which are usually identified by the use of words such as “anticipates,” “believes,” “continues,” “estimates,” “expects,” “hopes,” “intends,” “may,” “plans,” “projects,” “remains,” “seeks,” “should,” “will,” and variations of such words or similar expressions. BridgeBio intends these forward-looking statements to be covered by the safe harbor provisions for forward-looking statements contained in Section 27A of the Securities Act and Section 21E of the Exchange Act. These forward-looking statements, including express and implied statements relating to the continued commercial success and market potential of Attruby/Beyonttra (acoramidis); the Company’s expectations regarding timing of regulatory submissions and target action dates, approvals and commercial launches in the U.S. and Europe, including for BBP-418 for LGMD2I/R9, encaleret for ADH1, and oral infigratinib for achondroplasia; the Company’s expectations regarding the timing and outcome of pre-commercial activities, including activities designed to support three potential launches; the timing of the Company’s clinical trials, milestones and expected updates for its various programs and pipeline; the safety and the potential benefits of the Company’s product and product candidates; the Company’s anticipated presentations of data; and the Company’s belief that its cash, cash equivalents and marketable securities will enable the Company to fund its three potential launches and expansion indications across its pipeline. Such statements reflect the Company’s current views about the Company’s plans, intentions, expectations and strategies, which are based on the information currently available to it and on assumptions the Company has made. Although the Company believes that its plans, intentions, expectations and strategies as reflected in or suggested by those forward-looking statements are reasonable, the Company can give no assurance that the plans, intentions, expectations or strategies will be attained or achieved. Furthermore, actual results may differ materially from those described in the forward-looking statements and will be affected by a number of risks, uncertainties and assumptions, including, but not limited to, initial and ongoing data from the Company’s preclinical studies and clinical trials not being indicative of final data, the potential size of the target patient populations the Company’s product candidates are designed to treat not being as large as anticipated, the design and success of ongoing and planned clinical trials, future regulatory filings, approvals and/or sales, despite having ongoing and future interactions with the FDA or other regulatory agencies to discuss potential paths to registration for the Company’s product candidates, the FDA or such other regulatory agencies not agreeing with the Company’s regulatory approval strategies, components of the Company’s filings, such as clinical trial designs, conduct and methodologies, or the sufficiency of data submitted, the Company’s pre-commercial activities, commercial launches or operational execution not occurring on anticipated timelines or not supporting planned launches as expected, real-world experience with Attruby/Beyonttra not being consistent with observed biochemical differentiation or not translating into differentiated clinical, commercial or market outcomes, the continuing success of the Company’s collaborations, the Company’s ability to obtain additional funding, including through less dilutive sources of capital than equity financings, potential volatility in the Company’s share price, the Company’s share repurchase program being modified, suspended or discontinued, or share repurchases not delivering the anticipated benefits or proving to be a more attractive use of capital than other alternatives, the impacts of current macroeconomic and geopolitical events, including changing conditions from hostilities in Ukraine and the Middle East, increasing rates of inflation and changing interest rates, on business operations and expectations, as well as those risks set forth in the Risk Factors section of the Company’s most recent Quarterly Report on Form 10-Q and Annual Report on Form 10-K and the Company’s other filings with the U.S. Securities and Exchange Commission. Moreover, the Company operates in a very competitive and rapidly changing environment in which new risks emerge from time to time. These forward-looking statements are based upon the current expectations and beliefs of the Company’s management as of the date of this press release, and are subject to certain risks and uncertainties that could cause actual results to differ materially from those described in the forward-looking statements. Except as required by applicable law, BridgeBio assumes no obligation to update publicly any forward-looking statements, whether as a result of new information, future events or otherwise.
BridgeBio Media Contact:
Kaitlyn Reilly, Director, Communications
contact@bridgebio.com
(650)-789-8220
BridgeBio Investor Contact:
BridgeBio Investor Relations
ir@bridgebio.com
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