BBIO 8-K
BridgeBio Pharma, Inc. (BBIO)
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
FORM
CURRENT REPORT
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(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) |
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Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
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Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
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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:
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Trading |
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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 |
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Description |
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99.1 |
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104 |
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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.
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BridgeBio Pharma, Inc. |
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Date: |
August 3, 2023 |
By: |
/s/ Brian C. Stephenson |
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Brian C. Stephenson |
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:
Recent Corporate Updates:
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-$350 million of investment will support acoramidis from here through the first 12 months of commercial launch. This coupled with our slate of pivotal readouts over the next 24 months offers the opportunity for meaningful value creation for both patients and investors.”
BRIDGEBIO PHARMA, INC.
Condensed Consolidated Statements of Operations
(in thousands, except shares and per share amounts)
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Three Months Ended June 30, |
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Six Months Ended June 30, |
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2023 |
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2022 |
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2023 |
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2022 |
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(Unaudited) |
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(Unaudited) |
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Revenue |
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$ |
1,641 |
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$ |
73,746 |
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$ |
3,467 |
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$ |
75,440 |
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Operating costs and expenses: |
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Research, development and others |
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108,087 |
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109,100 |
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201,599 |
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218,097 |
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Selling, general and administrative |
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36,122 |
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36,426 |
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67,230 |
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80,139 |
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Restructuring, impairment and related charges |
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3,531 |
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8,396 |
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6,900 |
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31,058 |
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Total operating costs and expenses |
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147,740 |
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153,922 |
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275,729 |
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329,294 |
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Loss from operations |
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(146,099 |
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(80,176 |
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(272,262 |
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(253,854 |
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Other income (expense), net: |
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Interest income |
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4,514 |
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766 |
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8,667 |
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1,033 |
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Interest expense |
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(20,594 |
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(20,279 |
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(40,715 |
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(40,623 |
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Gain from sale of priority review voucher, net |
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— |
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107,946 |
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— |
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107,946 |
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Other income (expense), net |
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1,476 |
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(10,816 |
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875 |
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(18,391 |
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Total other income (expense), net |
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(14,604 |
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77,617 |
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(31,173 |
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49,965 |
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Net loss |
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(160,703 |
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(2,559 |
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(303,435 |
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(203,889 |
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Net loss (income) attributable to redeemable convertible |
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2,804 |
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(7,297 |
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5,380 |
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(2,364 |
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Net loss attributable to common stockholders |
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$ |
(157,899 |
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$ |
(9,856 |
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$ |
(298,055 |
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$ |
(206,253 |
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Net loss per share, basic and diluted |
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$ |
(0.98 |
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$ |
(0.07 |
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$ |
(1.90 |
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$ |
(1.41 |
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Weighted-average shares used in computing net |
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160,535,435 |
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146,684,804 |
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156,645,838 |
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146,285,694 |
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Three Months Ended June 30, |
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Six Months Ended June 30, |
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Stock-based Compensation |
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2023 |
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2022 |
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2023 |
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2022 |
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(Unaudited) |
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(Unaudited) |
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Research, development and others |
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$ |
13,229 |
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$ |
14,352 |
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$ |
25,008 |
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$ |
22,909 |
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Selling, general and administrative |
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13,947 |
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13,953 |
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25,645 |
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28,505 |
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Restructuring, impairment and related charges |
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— |
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— |
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— |
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1,172 |
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Total stock-based compensation |
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$ |
27,176 |
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$ |
28,305 |
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$ |
50,653 |
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$ |
52,586 |
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BRIDGEBIO PHARMA, INC.
Condensed Consolidated Balance Sheets
(In thousands)
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June 30, |
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December 31, |
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2023 |
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2022 |
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Assets |
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(Unaudited) |
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(1) |
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Cash and cash equivalents and marketable securities |
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$ |
333,307 |
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$ |
428,269 |
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Investment in equity securities |
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50,487 |
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43,653 |
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Receivable from licensing and collaboration agreements |
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8,614 |
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17,079 |
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Short-term restricted cash |
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19,930 |
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37,930 |
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Prepaid expenses and other current assets |
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20,546 |
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21,922 |
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Property and equipment, net |
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13,047 |
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14,569 |
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Operating lease right-of-use assets |
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9,814 |
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10,678 |
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Intangible assets, net |
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27,515 |
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28,712 |
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Other assets |
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20,401 |
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20,224 |
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Total assets |
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$ |
503,661 |
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$ |
623,036 |
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Liabilities, Redeemable Convertible Noncontrolling Interests and Stockholders’ Deficit |
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Accounts payable |
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$ |
3,874 |
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$ |
11,558 |
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Accrued and other liabilities |
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102,470 |
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|
106,195 |
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Operating lease liabilities |
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14,692 |
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15,949 |
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2029 Notes |
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735,940 |
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734,988 |
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2027 Notes |
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542,501 |
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541,634 |
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Term loan |
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440,496 |
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430,993 |
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Other long-term liabilities |
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13,326 |
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26,643 |
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Redeemable convertible noncontrolling interests |
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333 |
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(1,589 |
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Total BridgeBio stockholders' deficit |
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(1,362,023 |
) |
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(1,254,617 |
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Noncontrolling interests |
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12,052 |
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|
11,282 |
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Total liabilities, redeemable convertible noncontrolling interests and stockholders’ deficit |
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$ |
503,661 |
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$ |
623,036 |
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(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)
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Six Months Ended June 30, |
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2023 |
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2022 |
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Operating activities: |
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Net loss |
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$ |
(303,435 |
) |
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$ |
(203,889 |
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Adjustments to reconcile net loss to net cash used in operating activities: |
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Stock-based compensation |
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49,085 |
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52,409 |
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Depreciation and amortization |
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3,270 |
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3,466 |
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Noncash lease expense |
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2,024 |
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2,889 |
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Accrual of payment-in-kind interest on term loan |
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6,742 |
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— |
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Loss on deconsolidation of PellePharm |
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1,241 |
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— |
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(Gain) loss from investment in equity securities, net |
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(2,399 |
) |
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23,228 |
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Fair value of shares issued under a license agreement |
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— |
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4,567 |
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Accretion of debt |
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4,580 |
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|
4,383 |
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Fair value adjustment of warrants |
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(222 |
) |
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|
1,390 |
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Loss on sale of certain assets |
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— |
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|
6,261 |
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Impairment of long-lived assets |
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— |
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12,653 |
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Gain from sale of priority review voucher, excluding transaction costs |
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— |
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|
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(110,000 |
) |
Gain from recognition of receivable from licensing and collaboration agreement |
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— |
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|
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(12,500 |
) |
Other noncash adjustments |
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(328 |
) |
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|
853 |
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Changes in operating assets and liabilities: |
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Receivable from licensing and collaboration agreements |
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8,466 |
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|
2,993 |
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Prepaid expenses and other current assets |
|
|
1,057 |
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|
|
(3,021 |
) |
Other assets |
|
|
32 |
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|
8,691 |
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Accounts payable |
|
|
(4,098 |
) |
|
|
(3,090 |
) |
Accrued compensation and benefits |
|
|
(11,071 |
) |
|
|
(9,402 |
) |
Accrued research and development liabilities |
|
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(11,322 |
) |
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|
5,953 |
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Operating lease liabilities |
|
|
(2,443 |
) |
|
|
(3,348 |
) |
Deferred revenue |
|
|
(3,184 |
) |
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|
16,641 |
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Accrued professional and other liabilities |
|
|
4,330 |
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|
|
7,785 |
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Net cash used in operating activities |
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(257,675 |
) |
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(191,088 |
) |
Investing activities: |
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Purchases of marketable securities |
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(19,754 |
) |
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(119,611 |
) |
Maturities of marketable securities |
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41,550 |
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|
293,919 |
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Purchases of investment in equity securities |
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(71,504 |
) |
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|
(10,930 |
) |
Sales of investment in equity securities |
|
|
67,068 |
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|
9,708 |
|
Decrease in cash and cash equivalents resulting from deconsolidation of PellePharm |
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|
(503 |
) |
|
|
— |
|
Payment for an intangible asset |
|
|
— |
|
|
|
(1,500 |
) |
Proceeds from sale of priority review voucher |
|
|
— |
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|
|
110,000 |
|
Proceeds from sale of certain assets |
|
|
— |
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|
|
10,000 |
|
Purchases of property and equipment |
|
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(440 |
) |
|
|
(3,261 |
) |
Net cash provided by investing activities |
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|
16,417 |
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|
288,325 |
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Financing activities: |
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Proceeds from issuance of common stock through Follow-on offering, net |
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|
144,049 |
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|
|
— |
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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, |
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|
|
2023 |
|
|
2022 |
|
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Supplemental Disclosures of Cash Flow Information: |
|
|
|
|
|
|
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Cash paid for interest |
|
$ |
28,738 |
|
|
$ |
25,435 |
|
Supplemental Disclosures of Noncash Investing and Financing Information: |
|
|
|
|
|
|
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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 |
|
$ |
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
[email protected]
(650)-789-8220