8-K
0001743881false00017438812023-08-032023-08-03

 

UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549

 

FORM 8-K

 

CURRENT REPORT

Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934

Date of Report (Date of earliest event reported): August 3, 2023

 

 

BridgeBio Pharma, Inc.

(Exact name of Registrant as Specified in Its Charter)

 

 

Delaware

001-38959

84-1850815

(State or Other Jurisdiction
of Incorporation)

(Commission File Number)

(IRS Employer
Identification No.)

 

 

 

 

 

3160 Porter Dr., Suite 250

 

Palo Alto, CA

 

94304

(Address of Principal Executive Offices)

 

(Zip Code)

 

Registrant’s Telephone Number, Including Area Code: (650) 391-9740

 

Not Applicable

(Former Name or Former Address, if Changed Since Last Report)

 

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:

 

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)

 

 

Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)

 

 

Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))

 

 

Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

 

Securities registered pursuant to Section 12(b) of the Act:


Title of each class

 

Trading
Symbol(s)

 


Name of each exchange on which registered

Common Stock, par value $0.001 per share

 

BBIO

 

The Nasdaq Global Select Market

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§ 230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§ 240.12b-2 of this chapter).

Emerging growth company

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐

 

 


Item 2.02 Results of Operations and Financial Condition.

On August 3, 2023, BridgeBio Pharma, Inc. reported recent business updates and its financial results for the second quarter ended June 30, 2023. The full text of the press release issued in connection with the announcement is furnished as Exhibit 99.1 to this Current Report on Form 8-K.

 

The information in Item 2.02 of this Form 8-K (including Exhibit 99.1) shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended, or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference under the Securities Act of 1933, as amended, except as expressly set forth by specific reference in such a filing.

Item 9.01 Financial Statements and Exhibits.

(d) Exhibits.

Exhibit

 

Description

 

 

99.1

 

Press Release dated August 3, 2023, furnished herewith

 

 

104

 

Cover Page Interactive Data File (embedded within the Inline XBRL document)

 

 


SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

 

 

 

BridgeBio Pharma, Inc.

 

 

 

 

Date:

August 3, 2023

By:

/s/ Brian C. Stephenson

 

 

 

Brian C. Stephenson
Chief Financial Officer

 


EX-99.1

Exhibit 99.1

BridgeBio Pharma Reports Second Quarter 2023 Financial Results and Business Update

- Announced consistently positive results from the Phase 3 ATTRibute-CM study of acoramidis in patients with transthyretin amyloid cardiomyopathy (ATTR-CM), including a highly statistically significant result observed on the primary endpoint with a Win Ratio of 1.8 (p<0.0001) and clinically meaningful and consistent separation observed on measures of mortality, morbidity, function, and quality of life; the Company intends to file a New Drug Application (NDA) for acoramidis with the U.S. Food and Drug Administration (FDA) by the end of 2023

- Presented updated six-month results from Cohort 5 of PROPEL2, a Phase 2 trial of infigratinib in children with achondroplasia, at the Endocrine Society 2023 Annual Conference (ENDO 2023), demonstrating a continued potentially best-in-class efficacy and well-tolerated safety profile, and a mean increase in annualized height velocity (AHV) of 3.38cm/year with no treatment-related adverse events

- Dosed the first participant in FORTIFY, a global Phase 3 study of BBP-418 in patients with limb girdle muscular dystrophy type 2I/R9 (LGMD2I/R9) and met with the FDA to discuss the use of glycosylated alpha-dystroglycan (αDG) levels as a surrogate endpoint; based on this meeting, the Company believes there is potential to pursue Accelerated Approval in the U.S. for BBP-418

- Shared 18-month data from the long-term extension of the Phase 2 study of encaleret in patients with autosomal dominant hypocalcemia type 1 (ADH1) at ENDO 2023, including observation of a rapid and sustained treatment effect; Phase 3 CALIBRATE registrational trial remains ongoing, with topline results expected to be announced in the first half of 2024

- Phase 1/2 trial of BBP-631 for treatment of congenital adrenal hyperplasia (CAH) continuing to progress with an update planned by the end of 2023

- Three lead KRAS programs are advancing, with an Investigational New Drug (IND) application planned for first-in-class direct KRASG12C (ON) inhibitor BBO-8520 in 2023 as well as a recent selection of a clinical candidate for PI3Kα:RAS breaker with the intention to file an IND application in 2024

- Ended the quarter with $353 million in cash, cash equivalents, marketable securities, and short-term restricted cash, and $50 million of investments in equity securities, providing runway into 2H 2024

Palo Alto, CA – August 3, 2023 – BridgeBio Pharma, Inc. (Nasdaq: BBIO) (BridgeBio or the Company), a commercial-stage biopharmaceutical company focused on genetic diseases and cancers, today reported its financial results for the second quarter ended June 30, 2023 and provided an update on the Company’s operations.

“We’ll remain ever grateful for the support of the physicians and patients in the ATTR-CM community, which helped bring the ATTRibute-CM study to its final readout,” said Neil Kumar, Ph.D., founder and CEO of BridgeBio. “With these data in hand, coupled with a pipeline that could produce an additional three pivotal readouts in the next 24 months, we feel we have the ingredients to build a sustainable engine for the patients that we serve in large and small markets alike.”

BridgeBio’s key programs:

Acoramidis (AG10) – Transthyretin (TTR) stabilizer for transthyretin amyloid cardiomyopathy (ATTR-CM):

 

 

o
In July 2023, the Company released topline results from ATTRibute-CM, its Phase 3 trial of acoramidis for patients with ATTR-CM. The primary endpoint analysis was highly statistically significant with a Win Ratio of 1.8 (p<0.0001).
o
A clinically meaningful and consistent treatment effect was observed across all measures of mortality, morbidity, function, and quality of life.
o
An on-treatment survival rate of 81% was observed, versus a placebo survival rate of 74% (absolute risk reduction of 6.43%; relative risk reduction of 25%).
o
A highly statistically significant relative risk reduction of 50% (p<0.0001) was observed on frequency of cardiovascular-related hospitalization.
o
In comparative exploratory post hoc analyses enabled by tafamidis drop-in, albeit at low patient numbers, acoramidis showed a 42% greater increase in serum TTR levels and a 92% improvement in median NT-proBNP relative to placebo + tafamidis.
o
Acoramidis was well-tolerated with no safety signals of potential clinical concern identified.
o
BridgeBio intends to file an NDA for acoramidis with the FDA by end of 2023 and marketing authorization applications with additional regulatory authorities globally in 2024.
o
The details of the topline results of the ATTRibute-CM trial will be presented at the annual meeting of the European Society of Cardiology, one of the premier global cardiology congresses, in Amsterdam at the end of August 2023.
Low-dose infigratinib – FGFR1-3 inhibitor for achondroplasia and hypochondroplasia:
o
In June 2023, the Company presented updated six-month results from Cohort 5 of PROPEL2, its Phase 2 trial of infigratinib for children with achondroplasia, at ENDO 2023; the data demonstrated a significant and robust increase in annualized height velocity (AHV) with a mean change from baseline of +3.38 cm/year for 12 children.
o
83% of children in Cohort 5 responded to infigratinib, as defined by an increase from baseline AHV of at least 25%. The mean change from baseline in AHV of responders was +4.08 cm/year.
o
Early but promising trends towards improvement in proportionality were observed, as measured by the upper and lower body segment ratio.
o
At six months, infigratinib was well-tolerated as a single daily oral therapy with no adverse events assessed as treatment-related in all patients in Cohort 5.
o
The Company has started to enroll children in the run-in for a registrational Phase 3 trial.
o
If approved, BridgeBio believes that infigratinib has the potential to capture a significant share of the market based on blinded market research.
BBP-418 – Glycosylation substrate for limb-girdle muscular dystrophy type 2I/R9 (LGMD2I/R9):
o
The Company met with the FDA to discuss the use of glycosylated αDG levels as a surrogate endpoint. Based on this meeting, the Company believes there is potential to pursue Accelerated Approval in the U.S. for BBP-418.
o
The Company has dosed the first participant in FORTIFY, its global Phase 3 study of BBP-418 in patients with LGMD2I/R9.
o
FORTIFY includes an interim analysis at 12 months focused on change in glycosylated αDG levels; topline data from this analysis is expected in late 2024/early 2025.

 

 

o
Deficiency of glycosylated αDG is the causal molecular driver of LGMD2I/R9. In the ongoing Phase 2 study, patients treated with BBP-418 had a rapid and sustained increase of glycosylated αDG levels, concurrent with sustained decreases in creatine kinase and improvements from baseline in ambulatory and clinical function measures.
o
BBP-418 has a potentially addressable population of 7,000 patients in the United States and European Union.
o
There are currently no disease-modifying treatments available for LGMD2I/R9.
Encaleret – Calcium-sensing receptor (CaSR) inhibitor for autosomal dominant hypocalcemia type 1 (ADH1):
o
The Company presented 18-month data from the long-term extension of its Phase 2 study of encaleret in patients with ADH1 at ENDO 2023, including observations of a rapid and sustained treatment effect. Additionally, the Company shared initial findings from its genetic testing program, highlighting that ADH1 may be the most common presentation of nonsurgical hypoparathyroidism.
o
Population genetics analyses estimate approximately 25,000 carriers of gain-of-function variants of the CaSR, the underlying cause of ADH1, in the United States and European Union.
o
The Company anticipates sharing topline data from CALIBRATE, a Phase 3 registrational trial of encaleret for ADH1, in the first half of 2024.
o
If approved, encaleret could be the first therapy specifically indicated for the treatment of ADH1.
BBP-631 – AAV5 gene therapy candidate for congenital adrenal hyperplasia (CAH):
o
The Phase 1/2 gene therapy trial of BBP-631 for CAH continued to progress, and the Company plans to provide an update by the end of 2023.
o
CAH is one of the most prevalent genetic diseases potentially addressable with adeno-associated virus (AAV) gene therapy, with more than 75,000 cases estimated in the United States and European Union.
RAS cancer portfolio:
o
BridgeBio is continuing to develop the three main programs of its RAS franchise:
BBO-8520, an investigational, next-generation small molecule direct KRASG12C (ON) inhibitor candidate that is designed to directly bind and inhibit KRASG12C in both its ON (GTP-bound) and OFF (GDP-bound) conformations, which remains on track to file an IND application and enter the clinic in 2023.
A PI3Kα:RAS breaker program, investigational small molecules that are designed to block RAS-driven PI3Kα activation with a novel and potentially broad mechanism of action to target not only PI3Kα mutant tumors and RAS mutant tumors, but potentially other tumors driven by RTK activation of RAS signaling. The Company has selected a development candidate and expects to file an IND application in 2024 as the second investigational RAS cancer therapy from the BridgeBio portfolio.
The Company’s pan-KRAS program, which targets multiple KRAS mutants including KRASG12D and KRASG12V, which are present in a large percentage of colorectal, pancreatic,

 

 

and non-small cell lung cancer tumors. Development candidate selection for this program is planned for late 2023 or early 2024.

Recent Corporate Updates:

Partnership with Burjeel Holdings on project ‘NADER’ (Needs Assessment and Therapeutics Development for Rare Diseases – ‘nader’ meaning ‘rare’ in Arabic): Signed a preliminary, non-binding Collaboration Agreement establishing a mutual intention to revolutionize the field of early diagnosis and treatment of rare diseases in the United Arab Emirates and the region.
Updated encouraging clinical and biomarker data shared for the Company’s Canavan disease gene therapy program: Presented promising positive data from six participants dosed in CANaspire, the Company’s Phase 1/2 clinical trial of BBP-812, an investigational intravenous (IV) adeno-associated virus serotype 9 (AAV9) gene therapy for the treatment of Canavan disease. Following treatment, the N-acetylaspartate (NAA) levels of CANaspire participants were consistent with levels seen in individuals with milder Canavan disease based on findings from the Company’s natural history study and reports in the scientific literature. Sustained reductions in NAA were measured in the urine, cerebrospinal fluid (CSF), and brain of all participants and have been observed for over one year in the earliest dosed participants.

 

Second Quarter 2023 Financial Results:

 

Cash, Cash Equivalents, Marketable Securities and Short-Term Restricted Cash

 

Cash, cash equivalents, marketable securities and short-term restricted cash, totaled $353.2 million as of June 30, 2023, compared to $466.2 million as of December 31, 2022. The net decrease of $113.0 million in cash, cash equivalents, marketable securities and short-term restricted cash is primarily attributable to net cash used in operating activities of $257.7 million, offset by net proceeds received of $144.0 million from the Follow-on public offering during the six months ended June 30, 2023.

 

Revenue

 

Revenue for the three and six months ended June 30, 2023 was $1.6 million and $3.5 million, respectively, as compared to $73.7 million and $75.4 million for the same periods in the prior year. Revenue for the three and six months ended June 30, 2023 primarily consisted of $1.5 million and $3.2 million, respectively, of services revenue under the Navire-BMS License Agreement. Revenue for the three and six months ended June 30, 2022 primarily consisted of $70.2 million of license revenue and $3.2 million of services revenue under the Navire-BMS License Agreement.

 

Operating Costs and Expenses

 

Operating costs and expenses for the three and six months ended June 30, 2023 were $147.7 million and $275.7 million, respectively, compared to $153.9 million and $329.3 million for the same periods in the prior year. The overall decrease in operating costs and expenses for the three and six months ended June 30, 2023 compared to the comparative periods was due mainly to the decreases in research, development and other (R&D) expenses resulting from the Company's reprioritization of its R&D programs; selling, general and administrative expenses resulting from its company-wide streamlining of costs; and restructuring, impairment and related charges since the majority of the restructuring initiatives commenced in the first quarter of 2022.


 

 

The effects of the Company's restructuring initiative which commenced in the first quarter of 2022, continue to be realized due to the Company's reductions in operating costs and expenses. Restructuring, impairment and related charges for the three and six months ended June 30, 2023, amounted to $3.5 million and $6.9 million, respectively. These charges primarily consisted of winding down, exit costs, and severance and employee-related costs. Restructuring, impairment and related charges for the same periods in the prior year were $8.4 million and $31.1 million, respectively. These charges primarily consisted of impairments and write-offs of long-lived assets, severance and employee-related costs, and exit and other related costs. The Company remains committed to evaluating various restructuring alternatives aimed at driving operational changes in business processes. These alternatives includes enhancing commercialization efforts, improving efficiencies, and achieving cost savings.

 

Stock-based compensation expenses included in operating costs and expenses for the three months ended June 30, 2023 were $27.2 million, of which $13.2 million is included in research, development and other (R&D) expenses, $14.0 million is included in selling, general and administrative expenses. Stock-based compensation expenses included in operating costs and expenses for the three months ended June 30, 2022 were $28.3 million, of which $14.3 million is included in research, development and other (R&D) expenses, and $14.0 million is included in selling, general and administrative expenses.

 

Stock-based compensation expenses included in operating costs and expenses for the six months ended June 30, 2023 were $50.7 million, of which $25.0 million is included in research, development and other (R&D) expenses, $25.7 million is included in selling, general and administrative expenses. Stock-based compensation expenses included in operating costs and expenses for the six months ended June 30, 2022 were $52.6 million, of which $22.9 million is included in research, development and other (R&D) expenses, $28.5 million is included in selling, general and administrative expenses, and $1.2 million is included in restructuring, impairment and related charges.


“Following the recent announcement and strength of our Phase 3 ATTRibute-CM data, we will continue to explore multiple options to fully resource the acoramidis launch while optimizing cost of capital, including partnerships, royalty transactions, and equity financing,” said Brian Stephenson, Ph.D., CFA, Chief Financial Officer of BridgeBio. “We anticipate $300-$350 million of investment will support acoramidis from here through the first 12 months of commercial launch. This coupled with our slate of pivotal readouts over the next 24 months offers the opportunity for meaningful value creation for both patients and investors.”

 


 

 

 

BRIDGEBIO PHARMA, INC.

Condensed Consolidated Statements of Operations

(in thousands, except shares and per share amounts)

 

 

 

Three Months Ended June 30,

 

 

Six Months Ended June 30,

 

 

 

2023

 

 

2022

 

 

2023

 

 

2022

 

 

 

(Unaudited)

 

 

(Unaudited)

 

Revenue

 

$

1,641

 

 

$

73,746

 

 

$

3,467

 

 

$

75,440

 

Operating costs and expenses:

 

 

 

 

 

 

 

 

 

 

 

 

Research, development and others

 

 

108,087

 

 

 

109,100

 

 

 

201,599

 

 

 

218,097

 

Selling, general and administrative

 

 

36,122

 

 

 

36,426

 

 

 

67,230

 

 

 

80,139

 

Restructuring, impairment and related charges

 

 

3,531

 

 

 

8,396

 

 

 

6,900

 

 

 

31,058

 

Total operating costs and expenses

 

 

147,740

 

 

 

153,922

 

 

 

275,729

 

 

 

329,294

 

Loss from operations

 

 

(146,099

)

 

 

(80,176

)

 

 

(272,262

)

 

 

(253,854

)

Other income (expense), net:

 

 

 

 

 

 

 

 

 

 

 

 

Interest income

 

 

4,514

 

 

 

766

 

 

 

8,667

 

 

 

1,033

 

Interest expense

 

 

(20,594

)

 

 

(20,279

)

 

 

(40,715

)

 

 

(40,623

)

Gain from sale of priority review voucher, net

 

 

 

 

 

107,946

 

 

 

 

 

 

107,946

 

Other income (expense), net

 

 

1,476

 

 

 

(10,816

)

 

 

875

 

 

 

(18,391

)

Total other income (expense), net

 

 

(14,604

)

 

 

77,617

 

 

 

(31,173

)

 

 

49,965

 

Net loss

 

 

(160,703

)

 

 

(2,559

)

 

 

(303,435

)

 

 

(203,889

)

Net loss (income) attributable to redeemable convertible
   noncontrolling interests and noncontrolling interests

 

 

2,804

 

 

 

(7,297

)

 

 

5,380

 

 

 

(2,364

)

Net loss attributable to common stockholders
   of BridgeBio

 

$

(157,899

)

 

$

(9,856

)

 

$

(298,055

)

 

$

(206,253

)

Net loss per share, basic and diluted

 

$

(0.98

)

 

$

(0.07

)

 

$

(1.90

)

 

$

(1.41

)

Weighted-average shares used in computing net
   loss per share, basic and diluted

 

 

160,535,435

 

 

 

146,684,804

 

 

 

156,645,838

 

 

 

146,285,694

 

 

 

 

Three Months Ended June 30,

 

 

Six Months Ended June 30,

 

Stock-based Compensation

 

2023

 

 

2022

 

 

2023

 

 

2022

 

 

 

(Unaudited)

 

 

(Unaudited)

 

Research, development and others

 

$

13,229

 

 

$

14,352

 

 

$

25,008

 

 

$

22,909

 

Selling, general and administrative

 

 

13,947

 

 

 

13,953

 

 

 

25,645

 

 

 

28,505

 

Restructuring, impairment and related charges

 

 

 

 

 

 

 

 

 

 

 

1,172

 

Total stock-based compensation

 

$

27,176

 

 

$

28,305

 

 

$

50,653

 

 

$

52,586

 

 

 

 


 

 

 

BRIDGEBIO PHARMA, INC.

Condensed Consolidated Balance Sheets

(In thousands)

 

 

 

June 30,

 

 

December 31,

 

 

 

2023

 

 

2022

 

Assets

 

(Unaudited)

 

 

(1)

 

Cash and cash equivalents and marketable securities

 

$

333,307

 

 

$

428,269

 

Investment in equity securities

 

 

50,487

 

 

 

43,653

 

Receivable from licensing and collaboration agreements

 

 

8,614

 

 

 

17,079

 

Short-term restricted cash

 

 

19,930

 

 

 

37,930

 

Prepaid expenses and other current assets

 

 

20,546

 

 

 

21,922

 

Property and equipment, net

 

 

13,047

 

 

 

14,569

 

Operating lease right-of-use assets

 

 

9,814

 

 

 

10,678

 

Intangible assets, net

 

 

27,515

 

 

 

28,712

 

Other assets

 

 

20,401

 

 

 

20,224

 

Total assets

 

$

503,661

 

 

$

623,036

 

Liabilities, Redeemable Convertible Noncontrolling Interests and Stockholders’ Deficit

 

 

 

 

 

 

Accounts payable

 

$

3,874

 

 

$

11,558

 

Accrued and other liabilities

 

 

102,470

 

 

 

106,195

 

Operating lease liabilities

 

 

14,692

 

 

 

15,949

 

2029 Notes

 

 

735,940

 

 

 

734,988

 

2027 Notes

 

 

542,501

 

 

 

541,634

 

Term loan

 

 

440,496

 

 

 

430,993

 

Other long-term liabilities

 

 

13,326

 

 

 

26,643

 

Redeemable convertible noncontrolling interests

 

 

333

 

 

 

(1,589

)

Total BridgeBio stockholders' deficit

 

 

(1,362,023

)

 

 

(1,254,617

)

Noncontrolling interests

 

 

12,052

 

 

 

11,282

 

Total liabilities, redeemable convertible noncontrolling interests and stockholders’ deficit

 

$

503,661

 

 

$

623,036

 

 

(1)

The condensed consolidated financial statements as of and for the year ended December 31, 2022 are derived from the audited consolidated financial statements as of that date.

 

 

 


 

 

BRIDGEBIO PHARMA, INC.

Condensed Consolidated Statements of Cash Flows

(In thousands)

 

 

Six Months Ended June 30,

 

 

 

2023

 

 

2022

 

Operating activities:

 

 

 

 

 

 

Net loss

 

$

(303,435

)

 

$

(203,889

)

Adjustments to reconcile net loss to net cash used in operating activities:

 

 

 

 

 

 

Stock-based compensation

 

 

49,085

 

 

 

52,409

 

Depreciation and amortization

 

 

3,270

 

 

 

3,466

 

Noncash lease expense

 

 

2,024

 

 

 

2,889

 

Accrual of payment-in-kind interest on term loan

 

 

6,742

 

 

 

 

Loss on deconsolidation of PellePharm

 

 

1,241

 

 

 

 

(Gain) loss from investment in equity securities, net

 

 

(2,399

)

 

 

23,228

 

Fair value of shares issued under a license agreement

 

 

 

 

 

4,567

 

Accretion of debt

 

 

4,580

 

 

 

4,383

 

Fair value adjustment of warrants

 

 

(222

)

 

 

1,390

 

Loss on sale of certain assets

 

 

 

 

 

6,261

 

Impairment of long-lived assets

 

 

 

 

 

12,653

 

Gain from sale of priority review voucher, excluding transaction costs

 

 

 

 

 

(110,000

)

Gain from recognition of receivable from licensing and collaboration agreement

 

 

 

 

 

(12,500

)

Other noncash adjustments

 

 

(328

)

 

 

853

 

Changes in operating assets and liabilities:

 

 

 

 

 

 

Receivable from licensing and collaboration agreements

 

 

8,466

 

 

 

2,993

 

Prepaid expenses and other current assets

 

 

1,057

 

 

 

(3,021

)

Other assets

 

 

32

 

 

 

8,691

 

Accounts payable

 

 

(4,098

)

 

 

(3,090

)

Accrued compensation and benefits

 

 

(11,071

)

 

 

(9,402

)

Accrued research and development liabilities

 

 

(11,322

)

 

 

5,953

 

Operating lease liabilities

 

 

(2,443

)

 

 

(3,348

)

Deferred revenue

 

 

(3,184

)

 

 

16,641

 

Accrued professional and other liabilities

 

 

4,330

 

 

 

7,785

 

Net cash used in operating activities

 

 

(257,675

)

 

 

(191,088

)

Investing activities:

 

 

 

 

 

 

Purchases of marketable securities

 

 

(19,754

)

 

 

(119,611

)

Maturities of marketable securities

 

 

41,550

 

 

 

293,919

 

Purchases of investment in equity securities

 

 

(71,504

)

 

 

(10,930

)

Sales of investment in equity securities

 

 

67,068

 

 

 

9,708

 

Decrease in cash and cash equivalents resulting from deconsolidation of PellePharm

 

 

(503

)

 

 

 

Payment for an intangible asset

 

 

 

 

 

(1,500

)

Proceeds from sale of priority review voucher

 

 

 

 

 

110,000

 

Proceeds from sale of certain assets

 

 

 

 

 

10,000

 

Purchases of property and equipment

 

 

(440

)

 

 

(3,261

)

Net cash provided by investing activities

 

 

16,417

 

 

 

288,325

 

Financing activities:

 

 

 

 

 

 

Proceeds from issuance of common stock through Follow-on offering, net

 

 

144,049

 

 

 

 

Repayment of term loan

 

 

 

 

 

(20,486

)

Proceeds from BridgeBio common stock issuances under ESPP

 

 

1,809

 

 

 

966

 

Repurchase of shares to satisfy tax withholding

 

 

(1,715

)

 

 

(476

)

Issuance costs associated with term loan

 

 

 

 

 

(1,120

)

Proceeds from stock option exercises, net of repurchases

 

 

312

 

 

 

160

 

Other financing activities

 

 

4,563

 

 

 

 

Net cash provided by (used in) financing activities

 

 

149,018

 

 

 

(20,956

)

Net (decrease) increase in cash, cash equivalents and restricted cash

 

 

(92,240

)

 

 

76,281

 

Cash, cash equivalents and restricted cash at beginning of period

 

 

416,884

 

 

 

396,365

 

Cash, cash equivalents and restricted cash at end of period

 

$

324,644

 

 

$

472,646

 

 

 

 

Six Months Ended June 30,

 

 

 

2023

 

 

2022

 

Supplemental Disclosures of Cash Flow Information:

 

 

 

 

 

 

Cash paid for interest

 

$

28,738

 

 

$

25,435

 

Supplemental Disclosures of Noncash Investing and Financing Information:

 

 

 

 

 

 

Payment-in-kind interest added to principal of term loan

 

$

 

 

$

5,075

 

Unpaid property and equipment

 

$

131

 

 

$

73

 

Transfers (to) from noncontrolling interests

 

$

(5,940

)

 

$

1,456

 

Reconciliation of Cash, Cash Equivalents and Restricted Cash:

 

 

 

 

 

 

Cash and cash equivalents

 

$

302,438

 

 

$

470,098

 

Short-term restricted cash

 

 

19,930

 

 

 

 

Restricted cash — Included in “Prepaid expenses and other current assets”

 

 

 

 

 

140

 

Restricted cash — Included in “Other assets”

 

 

2,276

 

 

 

2,408

 

  Total cash, cash equivalents and restricted cash at end of period shown in the
   condensed consolidated statements of cash flows

 

$

324,644

 

 

$

472,646

 

 


 

 

 

 

About BridgeBio Pharma, Inc.

BridgeBio Pharma, Inc. (BridgeBio) is a commercial-stage biopharmaceutical company founded to discover, create, test, and deliver transformative medicines to treat patients who suffer from genetic diseases and cancers with clear genetic drivers. BridgeBio’s pipeline of development programs ranges from early science to advanced clinical trials. BridgeBio was founded in 2015 and its team of experienced drug discoverers, developers and innovators are committed to applying advances in genetic medicine to help patients as quickly as possible. For more information visit bridgebio.com and follow us on LinkedIn and Twitter.

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,” “estimates,” “expects,” “intends,” “may,” “plans,” “projects,” “seeks,” “should,” “will,” “on track”, “remains” and variations of such words or similar expressions. We intend 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 statements relating to the clinical and therapeutic, market potential of our programs and product candidates, including the statement in Dr. Kumar’s quote regarding our data, pipeline and potential product launches; the timing and success of our clinical development programs, including the progress of our ongoing and planned clinical trials of acoramidis for patients with ATTR-CM, our plans to file a new NDA for acoramidis with the FDA by end of year 2023, our planned marketing authorization applications with additional regulatory authorities in 2024, the planned presentation of the details of the topline results of ATTRibute-CM trial at the annual meeting of the European Society of Cardiology, and the availability of data from our clinical trials of acoramidis; the availability of data from our clinical trials of for BBP-418 in LGMD2I/R9, the potential and the opportunity to pursue Accelerated Approval Pathway for BBP-418 in LGMD2I/R9 in the U.S., and the potentially-addressable population of BBP-418 in the United States and European Union; the potential of infigratinib for achondroplasia to have a potential of best-in-class efficacy with well-tolerated safety profile and to capture a significant share of the market based on blinded market research, if approved; the Company’s finding that ADH1 may be the most common presentation of nonsurgical hypoparathyroidism, the timing and status of Phase 3 CALIBRATE registrational trial of encaleret for ADH1, the timing of announcement of topline data from CALIBRATE in the first half of 2024, and the success of encaleret (if approved), including its potential to be the first therapy specifically indicated for the treatment of ADH1; the continuation and progress of our ongoing Phase 1/2 trial of BBP-631 for CAH, with a planned update by the end of 2023; the continued development, the timing, progression and success of the RAS franchise, including an IND application planned for first-in-class direct KRASG12C (ON) inhibitor BBO-8520 in 2023, the intention to file an IND for a selected development candidate for PI3Kα:RAS breaker in 2024 as the second RAS cancer therapy from the BridgeBio portfolio, and the planned development candidate selection for the pan-KRAS program, for late 2023 or early 2024; our anticipated cash runway; the anticipated amounts needed to support our planned operations, including the potential commercial launch of acoramidis, and potential sources and availability of additional capital, reflect our current views about our plans, intentions, expectations and strategies, which are based on the information currently available to us and on assumptions we have made. Although we believe that our plans, intentions, expectations and strategies as reflected in or suggested by those forward-looking statements are reasonable, we 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 our preclinical studies and clinical trials not being indicative of final data, the potential size of the target patient populations our 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 our product candidates, the FDA or such other regulatory agencies not agreeing with our regulatory approval strategies, components of our filings, such as clinical trial designs, conduct and methodologies, or the sufficiency of data submitted, the continuing success of our collaborations, the Company’s ability to obtain additional funding under our credit facility or through potential partnerships, royalty transactions and equity financings, potential volatility in our share price, uncertainty regarding any impacts due to COVID-19, such as delays in regulatory review, manufacturing and supply chain interruptions, adverse effects on healthcare systems and disruption of the global economy, the impacts of current macroeconomic and geopolitical events, including changing conditions from hostilities in Ukraine, increasing rates of inflation and rising interest rates, on business operations and expectations, as well as those risks set forth in the Risk Factors section of our Annual Report on Form 10-K for the year ended December 31, 2022 and our other filings with the U.S. Securities and Exchange Commission. Moreover, we operate 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 our 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, we assume no obligation to update publicly any forward-looking statements, whether as a result of new information, future events or otherwise.

 

BridgeBio Contact:
Vikram Bali
contact@bridgebio.com
(650)-789-8220