Full Press Release Details
BridgeBio Reports Third Quarter 2025
Financial Results and Business Updates
-$120.7 million in total third quarter revenue, comprised of $108.1 million of U.S. Attruby net product revenue, $4.3 million from royalty revenue, and $8.3 million in license and services revenue
-As of October 25, 2025, 5,259 unique patient prescriptions have been written by 1,355 unique prescribers, representing an accelerating launch driven by strong month over month growth in the crucial treatment na ve patient segment
-Attruby continues to differentiate clinically by proving its unique profile in new subpopulations and holistic analyses
-JACC publication demonstrated the effect of Attruby on cumulative cardiovascular outcomes within the first month of treatment
-Positive topline interim analysis results from FORTIFY, the registrational Phase 3 study of BBP-418, a small molecule in development for LGMD2I R9
-Primary interim analysis endpoint, glycosylated DG, significantly increased by 1.8x change from baseline at 3 months (p 0.0001), and improvements were sustained at 12 months (p 0.0001) in BBP-418 treated individuals versus placebo
-Average reduction in serum CK, a marker of muscle damage, of 82% change from baseline and statistically significant difference versus placebo (p 0.0001) in BBP-418 treated individuals at 12 months
-Company intends to file an NDA for approval with the FDA in first half of 2026
-Positive topline results from CALIBRATE, the registrational Phase 3 study of encaleret for ADH1
-The primary endpoint was met with 76% of participants administered encaleret achieving both serum and urine calcium within the respective target ranges at Week 24 compared to 4% when on conventional therapy at Week 4 (p 0.0001)
- In a key secondary analysis, 91% of participants administered encaleret achieved intact PTH above the lower limit of the reference range at Week 24 compared to 7% of participants when on conventional therapy at Week 4 (p 0.0001)
-Company intends to submit an NDA to the FDA in first half of 2026 to support a full approval
-PROPEL 3, the registrational Phase 3 study of infigratinib for children with achondroplasia expects topline results in early 2026. Infigratinib has previously demonstrated best-in-class improvements in annualized height velocity and upper-to-lower body proportionality and was granted Breakthrough Therapy Designation by the FDA
-BridgeBio continues to grow potential impact of its medicines, with plans to share data from the Phase 3 portion of the ACCEL 2 3 study in hypochondroplasia in 2026, initiate clinical trials of encaleret in pediatric ADH1 and chronic hypoparathyroidism in 2026, and begin trials of BBP-418 in pediatric LGMD2I R9 and in LGMD2M 2U in the near term
-The Company ended the quarter with $645.9 million in cash, cash equivalents and marketable securities, well capitalized to commercialize Attruby and advance its late-stage pipeline
-Earnings call followed by Q A with investors and analysts today, October 29th at 4 30 pm ET
PALO ALTO, CA - October 29, 2025 - BridgeBio Pharma, Inc. (Nasdaq BBIO) ("BridgeBio" or the "Company"), a new type of biopharmaceutical company focused on genetic diseases, today announced its financial results for the third quarter ended September 30, 2025, and provided business updates.
As of October 25, 2025, 5,259 unique patient prescriptions have been written by 1,355 unique prescribers since FDA approval in November 2024. The third quarter revenue totaled $120.7 million, comprised of $108.1 million of U.S. Attruby net product revenue, $4.3 million from royalty revenue, and $8.3 million in license and services revenue.
"Attruby's first year on the market has been remarkable, with continued growth across all market segments and strong physician adoption that reflects both the differentiated clinical profile and the trust we're earning within the community. We're seeing meaningful momentum where prescribers are not only initiating more patients on therapy but continuing treatment, underscoring Attruby's real-world impact," said Matt Outten, Chief Commercial Officer of BridgeBio. "Importantly, this launch has also given us an invaluable blueprint for how we bring best-in-class medicines to patients with genetic diseases. With the promising results seen in BBP-418 for LGMD2I R9 and encaleret for ADH1, we are building on a proven commercial foundation to ensure these communities, each living with urgent, unmet needs, have timely access to transformative therapies and we will apply the playbook we've developed to prepare for our next potential approvals."
| Program | Status | Next expected milestone |
| Acoramidis for ATTR-CM | Approved in U.S., EU, Japan, and UK | New variant data to be shared at AHA Scientific Sessions |
| BBP-418 for LGMD2I R9 | FORTIFY, Phase 3 study interim analysis topline results released | File NDA with FDA in 1H 2026 |
| Encaleret for ADH1 | CALIBRATE, Phase 3 study topline results released | File NDA with FDA in 1H 2026 |
| Infigratinib for achondroplasia | PROPEL 3, Phase 3 study enrollment completed | Topline results in early 2026 |
| Encaleret for chronic hypoparathyroidism | Phase 2 proof-of-principle study completed | Phase 3 study to be initiated in 2026 |
| Infigratinib for hypochondroplasia | ACCEL 2 3, Phase 2 study first participant dosed | Enrollment completion for Phase 2 portion by end of 2025 |
"Attruby's strong commercial performance continues to validate our model, delivering a potential best-in-class medicine to patients who were historically overlooked and building meaningful momentum across all market segments," said Neil Kumar, Ph.D., founder and CEO of BridgeBio. "We are now seeing that same success echoed in our pipeline with home-run data in both ADH1 and
LGMD2I R9, and we continue to advance one of the broadest and fastest-moving portfolios in genetic medicine. With achondroplasia data expected in 2026, enrollment nearing completion for the Phase 2 potion of the hypochondroplasia study, and registrational studies for encaleret in chronic hypoparathyroidism and pediatric ADH1 planned next year, we are not slowing down and continue to be impatient for patients. These milestones reflect our growing scalability and strengthen our conviction that BridgeBio is only beginning to show what's possible as we evolve into a durable, multi-medicine company built for patients with genetic diseases for decades to come."
Attruby (acoramidis) - First near-complete ( 90%) transthyretin (TTR) stabilizer for treatment of transthyretin amyloid cardiomyopathy (ATTR-CM)
At this year's Heart Failure Society of America (HFSA) Annual Scientific Meeting, BridgeBio presented data from the ATTRibute-CM study showing that acoramidis reduced cumulative cardiovascular outcomes, including cardiovascular mortality (CVM) or recurrent cardiovascular-related hospitalizations (CVH), within the first month of treatment in patients with ATTR-CM. At Month 30, Acoramidis significantly reduced the cumulative risk of CVM or recurrent CVH versus placebo with a 49% hazard reduction (p 0.0001). Acoramidis also showed that 53 events were avoided per 100 treated participants (95% CI 29-79) at Month 30. These data were presented in a Late Breaking Clinical Trials Oral Presentation at the HFSA Annual Scientific Meeting 2025 and simultaneously published in Journal of the American College of Cardiology (JACC).
Earlier in the year at the European Society of Cardiology Congress, BridgeBio shared a post-hoc analysis of ATTRibute-CM, demonstrating a significant reduction in risk of CVM through 42 months post-randomization, with a 44% hazard reduction, setting a new standard for CVM outcomes for patients with ATTR-CM. Acoramidis also demonstrated a significant 46% hazard reduction in the risk of the composite outcome of CVM or first CVH through 42 months.
More data on Attruby will be shared at the American Heart Association (AHA) Congress in November 2025 and in medical congresses throughout 2026.
BBP-418 - Glycosylation substrate for limb-girdle muscular dystrophy type 2I R9 (LGMD2I R9)
FORTIFY, the Phase 3 clinical trial of BBP-418, successfully achieved all primary and secondary endpoints of its interim analysis.
Findings included a highly statistically significant increase of 1.8x change from baseline (p 0.0001) of glycosylated alpha-dystroglycan ( DG) observed in the BBP-418 group compared to approximately no change in the placebo group from baseline to 3 months, which was sustained at 12 months (p 0.0001).
An average reduction in serum creatine kinase (CK), a marker of muscle breakdown, of 82% change from baseline (p 0.0001) was observed in BBP-418 treated individuals.
Importantly, statistically significant and clinically meaningful improvements in ambulation 100-meter timed test (100MTT) velocity, p 0.0001 and pulmonary function forced vital capacity (FVC) % predicted, sitting position, p 0.0071 were also observed at 12 months in the BBP-418 group compared with the placebo group.
BBP-418 was well-tolerated with no new or unexpected safety findings observed.
BridgeBio intends to file a New Drug Application (NDA) for approval with the FDA in the first half of 2026.
If successful, BBP-418 could be the first approved therapy for individuals living with LGMD2I R9, potentially representing the first approval of a therapy for any form of LGMD.
The Company intends to initiate clinical studies of BBP-418 in LGMD2I R9 for individuals less than 12 years of age and in LGMD2M 2U in the near future.
Encaleret - Calcium-sensing receptor (CaSR) antagonist for autosomal dominant hypocalcemia type 1 (ADH1) and chronic hypoparathyroidism
CALIBRATE, the Phase 3 clinical trial of oral encaleret in ADH1, a genetic form of hypoparathyroidism, successfully achieved all pre-specified primary and key secondary efficacy endpoints.
The primary endpoint was met with 76% of participants administered encaleret achieving both serum and urine calcium within the respective target ranges at Week 24 compared to 4% when on conventional therapy at Week 4 (p 0.0001).
In a key secondary analysis, 91% of participants administered encaleret achieved intact parathyroid hormone above the lower limit of the reference range at Week 24 compared to 7% of participants when on conventional therapy at Week 4 (p 0.0001).
Encaleret was well-tolerated with no discontinuations related to study drug.
BridgeBio intends to submit a NDA to the FDA in the first half of 2026, and a Marketing Authorization Application to the European Medicines Agency to follow.
If approved, encaleret would be the first therapy indicated for individuals living with ADH1.
The Company plans to initiate a registrational clinical trial of encaleret in pediatric ADH1 in the first quarter of 2026
The Company also plans to initiate a Phase 3 study of encaleret in chronic hypoparathyroidism in 2026.
Infigratinib - FGFR1-3 inhibitor for achondroplasia and hypochondroplasia
PROPEL 3, the Phase 3 clinical trial of infigratinib in achondroplasia, the most common form of disproportionate short stature, is fully enrolled with 114 participants randomized.
BridgeBio expects topline results of PROPEL 3 in early 2026.
BridgeBio has reached regulatory alignment with the FDA on the clinical development plan for infigratinib in infants and toddlers with achondroplasia from birth to less than 3 years old. Based on the discussion, the Company initiated clinical development in this important age range.
The first participant in the Phase 2 portion of ACCEL 2 3 in hypochondroplasia was dosed in April 2025 and the Company expects to fully enroll the Phase 2 portion of the study by the end of 2025. The Phase 2 data is expected in the second half of 2026.
Infigratinib demonstrates single-digit nanomolar potency in vitro across causative FGFR3 variants in hypochondroplasia, consistent with its activity in achondroplasia, highlighting robust preclinical efficacy across FGFR3-driven skeletal dysplasias (Demuynck et al., JBMR, 2025).
In achondroplasia, infigratinib has received Breakthrough Designation from the FDA, Orphan Drug Designation, Fast Track Designation, and Rare Pediatric Disease Designation. To date, in hypochondroplasia, infigratinib has received Fast Track Designation and Orphan Drug Designation from the FDA and EMA.
If successful, infigratinib would be the first approved oral therapy option for children living with achondroplasia and hypochondroplasia.
Cash, Cash Equivalents and Marketable Securities
Cash, cash equivalents and marketable securities totaled $645.9 million as of September 30, 2025, compared to cash and cash equivalents of $681.1 million as of December 31, 2024. The $35.2 million
decrease is primarily attributable to net cash used in operating activities of $389.5 million for the nine months ended September 30, 2025, the repayment of the Company's previous term loan under its credit facility (including prepayment fees) of $459.0 million in February 2025, and the repurchase of common stock of $48.3 million using proceeds from the 2031 Notes in February 2025. These outflows were partially offset by net proceeds of $563.0 million from the issuance of the 2031 Notes in February 2025 and net proceeds of $297.0 million from the execution of the Royalty Interest Purchase and Sale Agreement with HealthCare Royalty, a related party, and Blue Owl Capital in June 2025.
| Three Months Ended September 30, | Nine Months Ended September 30, | ||||||||||||||
| 2025 | 2024 | 2025 | 2024 | ||||||||||||
| (in thousands) | |||||||||||||||
| Net product revenue | $ | 108,111 | $ | - | $ | 216,351 | $ | - | |||||||
| License and services revenue | 8,311 | 2,732 | 125,441 | 216,020 | |||||||||||
| Royalty revenue | 4,278 | - | 6,106 | - | |||||||||||
| Total revenues, net | $ | 120,700 | $ | 2,732 | $ | 347,898 | $ | 216,020 |
Total revenues, net for the three months ended September 30, 2025, were $120.7 million compared to $2.7 million for the same period in the prior year. The $118.0 million increase was primarily driven by a $108.1 million increase in net product revenue from the Company's commercial product, Attruby, a $5.6 million increase in license and services revenue, and a $4.3 million increase in royalty revenue earned on net product sales of BEYONTTRA in the EU and Japan.
Total revenues, net for the nine months ended September 30, 2025, were $347.9 million compared to $216.0 million for the same period in the prior year. The $131.9 million increase was primarily driven by a $216.4 million increase in net product revenue from the Company's commercial product, Attruby, and a $6.1 million increase in royalty revenue earned on net product sales of BEYONTTRA in the EU and Japan. These increases were partially offset by a $90.6 million decrease in license and services revenue, reflecting the timing of recognition of upfront payments from the Company's exclusive license agreements with collaboration partners as well as regulatory-related milestones recognized upon the approval of BEYONTTRA in the EU and pricing approval in Japan.
Operating Costs and Expenses
| Three Months Ended September 30, | Nine Months Ended September 30, | ||||||||||||||
| 2025 | 2024 | 2025 | 2024 | ||||||||||||
| (in thousands) | |||||||||||||||
| Total cost of revenues | $ | 6,563 | $ | 598 | $ | 12,855 | $ | 1,794 | |||||||
| Research and development | 112,874 | 120,444 | 335,536 | 376,111 | |||||||||||
| Selling, general and administrative | 137,621 | 68,819 | 373,140 | 194,149 | |||||||||||
| Restructuring, impairment and related charges | 8,841 | 4,621 | 10,216 | 10,912 | |||||||||||
| Total operating costs and expenses | $ | 265,899 | $ | 194,482 | $ | 731,747 | $ | 582,966 |
Operating costs and expenses for the three months ended September 30, 2025 were $265.9 million compared to $194.5 million for the same period in the prior year. The $71.4 million increase was primarily driven by a $68.8 million increase in selling, general and administrative ("SG A") expenses largely reflecting the Company's investments in support of the commercial launch and ongoing activities of Attruby, and a $6.0 million increase in total cost of revenues, primarily due to the cost of
Attruby products sold. These increases were partially offset by a $7.6 million decrease in research and development ( R D ) expenses as a result of the Company's reprioritization of its R D programs.
Operating costs and expenses for the nine months ended September 30, 2025 were $731.7 million compared to $583.0 million for the same period in the prior year. The $148.7 million increase was primarily driven by a $179.0 million increase in SG A largely reflecting the Company's investments to support the commercial launch and ongoing activities of Attruby, and an $11.1 million increase in total cost of revenues, primarily due to the cost of Attruby products sold. The increases were partially offset by a $40.6 million decrease in R D expenses as a result of the Company's reprioritization of its R D programs.
Stock-based compensation expenses included in operating costs and expenses for the three months ended September 30, 2025 were $35.3 million, of which $21.9 million is included in SG A expenses, $12.3 million is included in R D expenses, $0.7 million is included in restructuring impairment and related charges, and $0.4 million is included in cost of goods sold. Stock-based compensation expenses included in operating costs and expenses for the same period in 2024 were $27.1 million, of which $15.0 million was included in SG A expenses and $12.1 million was included in R D expenses.
Stock-based compensation expenses included in operating costs and expenses for the nine months ended September 30, 2025 were $102.0 million, of which $63.1 million is included in SG A expenses, $37.5 million is included in R D expenses, $0.8 million is included in restructuring impairment and related charges, and $0.6 million is included in cost of goods sold. Stock-based compensation expenses included in operating costs and expenses for the same period in the prior year were $77.4 million, of which $47.5 million was included in SG A expenses and $29.8 million was included in R D expenses, and $0.1 million was included in restructuring, impairment and related charges.
Total Other Income (Expense), Net
Total other income (expense), net for the three and nine months ended September 30, 2025, was $(41.3) million and $(153.9) million, respectively, compared to $27.5 million and $91.0 million, respectively, for the same periods in the prior year.
The change in total other income (expense), net of $68.8 million for the three months ended September 30, 2025, compared to 2024 was primarily due to a decrease in gain on deconsolidation of subsidiaries of $52.0 million, and an increase in noncash interest expense on deferred royalty obligations of $36.4 million, partially offset by a decrease in interest expense of $11.3 million, and an increase in other income of $7.8 million related to noncash income from the Company's equity method investment.
The change in total other income (expense), net of $244.9 million for the nine months ended September 30, 2025, compared to 2024 was primarily due to a decrease in gain on deconsolidation of subsidiaries of $178.3 million, an increase in noncash interest expense on deferred royalty obligations of $86.5 million, and an increase in net loss from equity method investments of $37.1 million partially offset by a decrease in interest expense of $28.0 million, an increase in other income of $11.1 million for the change in fair value of the embedded derivative liability component of the Company's deferred royalty obligation, an increase in other income of $7.5 million for services provided under the transition service agreements, and an increase in other income of $7.8 million related to noncash income from the Company's equity method investment.
Net Loss Attributable to Common Stockholders of BridgeBio and Net Loss per Share
For the three and nine months ended September 30, 2025, the Company recorded a net loss attributable to common stockholders of BridgeBio of $182.7 million and $532.1 million, respectively, compared to $162.0 million and $270.7 million, respectively, for the same periods in the prior year.
For the three and nine months ended September 30, 2025, the Company reported a net loss per share of $0.95 and $2.79, respectively, compared to $0.86 and $1.46, respectively, for the same periods in the prior year.
BRIDGEBIO PHARMA, INC.
Condensed Consolidated Statements of Operations
(in thousands, except shares and per share amounts)
| Three Months Ended September 30, | Nine Months Ended September 30, | ||||||||||||||
| 2025 | 2024 | 2025 | 2024 | ||||||||||||
| (Unaudited) | (Unaudited) | ||||||||||||||
| Revenues | |||||||||||||||
| Net product revenue | $ | 108,111 | $ | - | $ | 216,351 | $ | - | |||||||
| License and services revenue | 8,311 | 2,732 | 125,441 | 216,020 | |||||||||||
| Royalty revenue | 4,278 | - | 6,106 | - | |||||||||||
| Total revenues, net | 120,700 | 2,732 | 347,898 | 216,020 | |||||||||||
| Operating costs and expenses | |||||||||||||||
| Cost of revenues | |||||||||||||||
| Cost of goods sold | 4,028 | - | 8,910 | - | |||||||||||
| Cost of license, services and royalty revenue | 2,535 | 598 | 3,945 | 1,794 | |||||||||||
| Total cost of revenues | 6,563 | 598 | 12,855 | 1,794 | |||||||||||
| Research and development | 112,874 | 120,444 | 335,536 | 376,111 | |||||||||||
| Selling, general and administrative | 137,621 | 68,819 | 373,140 | 194,149 | |||||||||||
| Restructuring, impairment and related charges | 8,841 | 4,621 | 10,216 | 10,912 | |||||||||||
| Total operating costs and expenses | 265,899 | 194,482 | 731,747 | 582,966 | |||||||||||
| Loss from operations | (145,199) | (191,750) | (383,849) | (366,946) | |||||||||||
| Other income (expense), net | |||||||||||||||
| Interest income | 6,239 | 3,296 | 15,522 | 12,566 | |||||||||||
| Interest expense | (11,739) | (23,061) | (41,467) | (69,469) | |||||||||||
| Noncash interest expense on deferred royalty obligations (1) | (36,410) | - | (86,460) | - | |||||||||||
| Gain on deconsolidation of subsidiaries | - | 52,027 | - | 178,321 | |||||||||||
| Loss on extinguishments of debt | - | - | (21,155) | (26,590) | |||||||||||
| Net loss from equity method investments | (15,834) | (6,563) | (51,579) | (14,488) | |||||||||||
| Other income, net | 16,461 | 1,797 | 31,240 | 10,648 | |||||||||||
| Total other income (expense), net | (41,283) | 27,496 | (153,899) | 90,988 | |||||||||||
| Loss before income taxes | (186,482) | (164,254) | (537,748) | (275,958) | |||||||||||
| Provision for (benefit from) income taxes | (1,545) | - | 555 | - | |||||||||||
| Net loss | (184,937) | (164,254) | (538,303) | (275,958) | |||||||||||
| Net loss attributable to redeemable convertible noncontrolling interests and noncontrolling interests | 2,194 | 2,214 | 6,235 | 5,246 | |||||||||||
| Net loss attributable to common stockholders of BridgeBio | $ | (182,743) | $ | (162,040) | $ | (532,068) | $ | (270,712) | |||||||
| Net loss per share attributable to common stockholders of BridgeBio, basic and diluted | $ | (0.95) | $ | (0.86) | $ | (2.79) | $ | (1.46) | |||||||
| Weighted-average shares used in computing net loss per share attributable to common stockholders of BridgeBio, basic and diluted | 191,854,152 | 188,510,372 | 190,845,133 | 184,947,173 |
(1)Including related party amounts of $(5,383) and $(5,560) for the three and nine months ended September 30, 2025, respectively.
| Three Months Ended September 30, | Nine Months Ended September 30, | ||||||||||||||
| Stock-based Compensation | 2025 | 2024 | 2025 | 2024 | |||||||||||
| (Unaudited) | (Unaudited) | ||||||||||||||
| Cost of goods sold | $ | 361 | $ | - | $ | 578 | $ | - | |||||||
| Research and development | 12,328 | 12,124 | 37,582 | 29,840 | |||||||||||
| Selling, general and administrative | 21,866 | 14,969 | 63,077 | 47,511 | |||||||||||
| Restructuring, impairment and related charges | 709 | 38 | 755 | 81 | |||||||||||
| Total stock-based compensation | $ | 35,264 | $ | 27,131 | $ | 101,992 | $ | 77,432 |
BRIDGEBIO PHARMA, INC.
Condensed Consolidated Balance Sheets
| September 30, 2025 | December 31, 2024 | ||||||
| (Unaudited) | (1) | ||||||
| Assets | |||||||
| Cash, cash equivalents and marketable securities | $ | 645,942 | $ | 681,101 | |||
| Accounts receivable, net | 116,518 | 4,722 | |||||
| Inventories | 24,527 | - | |||||
| Prepaid expenses and other current assets | 52,395 | 34,869 | |||||
| Investment in nonconsolidated entities | 92,168 | 143,747 | |||||
| Property and equipment, net | 5,830 | 7,011 | |||||
| Operating lease right-of-use assets | 6,553 | 5,767 | |||||
| Intangible assets, net | 28,795 | 23,926 | |||||
| Other assets | 25,522 | 18,195 | |||||
| Total assets | $ | 998,250 | $ | 919,338 | |||
| Liabilities, Redeemable Convertible Noncontrolling Interests and Stockholders' Deficit | |||||||
| Accounts payable | $ | 18,702 | $ | 9,618 | |||
| Accrued and other current liabilities (2) | 183,517 | 125,672 | |||||
| Operating lease liabilities | 8,721 | 9,202 | |||||
| Deferred revenue | 22,218 | 31,699 | |||||
| 2031 Notes, net | 564,087 | - | |||||
| 2029 Notes, net | 740,380 | 738,872 | |||||
| 2027 Notes, net | 546,549 | 545,173 | |||||
| Term loan, net | - | 437,337 | |||||
| Deferred royalty obligations, net (3) | 836,126 | 479,091 | |||||
| Other long-term liabilities | 679 | 286 | |||||
| Redeemable convertible noncontrolling interests | 23 | 142 | |||||
| Total BridgeBio stockholders' deficit | (1,933,070) | (1,467,904) | |||||
| Noncontrolling interests | 10,318 | 10,150 | |||||
| Total liabilities, Redeemable Convertible Noncontrolling Interests and Stockholders' Deficit | $ | 998,250 | $ | 919,338 |
(1)The condensed consolidated financial statements as of and for the year ended December 31, 2024 are derived from the audited consolidated financial statements as of that date.
(2)Including a related party amount of $1,647 as of September 30, 2025.
(3)Including a related party amount of $201,242 as of September 30, 2025.
BRIDGEBIO PHARMA, INC.
Condensed Consolidated Statements of Cash Flows
| Nine Months Ended September 30, | |||||||
| 2025 | 2024 | ||||||
| Operating activities | |||||||
| Net loss | $ | (538,303) | $ | (275,958) | |||
| Adjustments to reconcile net loss to net cash used in operating activities | |||||||
| Stock-based compensation | 98,385 | 65,673 | |||||
| Loss on extinguishments of debt | 21,155 | 26,590 | |||||
| Noncash interest expense on deferred royalty obligations (1) | 86,460 | - | |||||
| Amortization of debt discount and issuance costs | 4,515 | 5,399 | |||||
| Depreciation and amortization | 3,999 | 4,708 | |||||
| Noncash lease expense | 3,443 | 3,119 | |||||
| Net loss from equity method investments | 51,579 | 14,488 | |||||
| Change in fair value of the embedded derivative associated with the deferred royalty obligation | (11,062) | - | |||||
| Noncash income from an equity method investment | (7,769) | - | |||||
| Gain on deconsolidation of subsidiaries | - | (178,321) | |||||
| Gain from investment in equity securities, net | - | (8,136) | |||||
| Other noncash adjustments, net | (1,217) | (2,059) | |||||
| Changes in operating assets and liabilities | |||||||
| Accounts receivable, net | (111,796) | 1,273 | |||||
| Inventories | (23,356) | - | |||||
| Prepaid expenses and other current assets | (17,527) | (17,543) | |||||
| Other assets | 568 | (428) | |||||
| Accounts payable | 9,084 | 5,257 | |||||
| Accrued compensation and benefits | 3,212 | 5,580 | |||||
| Accrued research and development liabilities | 347 | 15,454 | |||||
| Operating lease liabilities | (4,757) | (4,459) | |||||
| Deferred revenue | (9,480) | 20,575 | |||||
| Other liabilities (2) | 53,030 | (6,612) | |||||
| Net cash used in operating activities | (389,490) | (325,400) | |||||
| Investing activities | |||||||
| Purchases of marketable securities | (10,876) | (93,811) | |||||
| Maturities of marketable securities | 8,000 | 95,000 | |||||
| Purchases of investments in equity securities | - | (20,271) | |||||
| Proceeds from sales of investments in equity securities | - | 63,229 | |||||
| Proceeds from special cash dividends received from an investment in equity securities | 2,302 | 25,682 | |||||
| Payment for intangible assets | (8,495) | (4,785) | |||||
| Purchases of property and equipment | (1,064) | (886) | |||||
| Decrease in cash and cash equivalents resulting from deconsolidation of subsidiaries | - | (140) | |||||
| Net cash provided by (used in) investing activities | (10,133) | 64,018 | |||||
| Financing activities | |||||||
| Proceeds from issuance of 2031 Notes | 575,000 | - | |||||
| Issuance costs and discounts associated with 2031 Notes | (12,034) | - | |||||
| Repurchase of common stock | (48,276) | - | |||||
| Proceeds from a royalty obligation under the Royalty Purchase Agreement | 300,000 | - | |||||
| Issuance costs associated with a royalty obligation under the Royalty Purchase Agreement | (3,010) | - | |||||
| Proceeds from term loan under the Amended Financing Agreement | - | 450,000 | |||||
| Issuance costs and discounts associated with term loan under the Amended Financing Agreement | - | (15,986) | |||||
| Repayment of term loans | (459,000) | (473,417) | |||||
| Repayments of deferred royalty obligations (3) | (6,896) | - | |||||
| Proceeds from issuance of common stock through public offerings, net | - | 314,741 |
| Proceeds from common stock issuances under ESPP | 6,414 | 4,502 | |||||
| Proceeds from stock option exercises, net of repurchases | 14,523 | 808 | |||||
| Transactions with noncontrolling interests | 1,550 | - | |||||
| Repurchase of RSU shares to satisfy tax withholding | (6,796) | (6,122) | |||||
| Net cash provided by financing activities | 361,475 | 274,526 | |||||
| Net increase (decrease) in cash, cash equivalents and restricted cash | (38,148) | 13,144 | |||||
| Cash, cash equivalents and restricted cash at beginning of period | 683,244 | 394,732 | |||||
| Cash, cash equivalents and restricted cash at end of period | $ | 645,096 | $ | 407,876 |
(1)Including a related party amount of $5,560 for the nine months ended September 30, 2025.
(2)Including a related party amount of $1,647 for the nine months ended September 30, 2025.
(3)Including a related party amount of $(665) for the nine months ended September 30, 2025.
| Nine Months Ended September 30, | |||||||
| 2025 | 2024 | ||||||
| Supplemental Disclosure of Cash Flow Information | |||||||
| Cash paid for interest | $ | 43,670 | $ | 78,236 | |||
| Cash paid for income taxes | $ | 1,153 | $ | - | |||
| Supplemental Disclosures of Noncash Investing and Financing Information | |||||||
| Unpaid property and equipment | $ | 12 | $ | 274 | |||
| Transfers to noncontrolling interests | $ | (4,734) | $ | (4,719) | |||
| Reconciliation of Cash, Cash Equivalents and Restricted Cash | |||||||
| Cash and cash equivalents | $ | 642,951 | $ | 266,324 | |||
| Restricted cash - Included in "Prepaid expenses and other current assets" | 126 | 139,409 | |||||
| Restricted cash - Included in "Other assets" | 2,019 | 2,143 | |||||
| Total cash, cash equivalents and restricted cash at end of periods shown in the condensed consolidated statements of cash flows | $ | 645,096 | $ | 407,876 |
BridgeBio will host its quarterly earnings call and simultaneous webcast on Wednesday, October 29th 2025 at 4 30 pm ET. To access the live webcast of BridgeBio's presentation, please visit the "Events" page within the Investors section of the BridgeBio website at https investor.bridgebio.com news-and-events event-calendar or register online using the following link, https events.q4inc.com attendee 108071157. A replay of the conference call and webcast will be archived on the Company's website and will be available for at least 30 days following the event.
About Attruby (acoramidis)
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
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.