Full Press Release Details
BridgeBio Pharma, Inc. Reports First Quarter 2020 Financial Results and Business Update
-Ended quarter with $928 million in cash, cash equivalents and marketable securities
SAN FRANCISCO, May 13, 2020 BridgeBio Pharma, Inc. (Nasdaq: BBIO), today reported its financial results for the first
quarter ended March 31, 2020 and provided an update on the company s operations.
The company is working with its committed partners to minimize
disruption from the COVID-19 pandemic on its clinical trials and other drug development programs. BridgeBio salutes the brave physicians, nurses, first responders and medical staff who are working across the
globe to care for patients with COVID-19.
BridgeBio s fully enrolled trials and preclinical programs are
moving ahead with minimal delays, and the company is on track to file its second New Drug Application (NDA) later this year, along with the anticipated filing of multiple investigational new drug applications (INDs). Despite the challenges presented
by COVID-19, BridgeBio s clinical trials of infigratinib in tumors with FGFR genetic alterations are proceeding as planned.
Certain clinical trials that were in the process of enrolling have slowed as a result of the COVID-19 outbreak.
BridgeBio is working with hospitals and investigators to deliver investigational medicines to patients and to develop solutions that will allow the company to continue to measure key endpoints for these trials. BridgeBio is also prepared to continue
enrolling patients as the healthcare system regains the ability to accommodate this activity.
For trials that have not yet begun enrolling, BridgeBio is
prepared to begin them as soon as trial sites can accommodate enrollment. Given the severe and often life-threatening nature of many of the disease areas on which BridgeBio is focused, we anticipate many of our planned trials will be prioritized.
Given COVID-19 s impact, we estimate that certain milestones related to clinical trials that were
anticipated in 2020 are now more likely to come in 2021. Other programs are moving forward without delay, thanks to the committed efforts of our partners, said BridgeBio founder and CEO Neil Kumar, Ph.D. We believe we are in a position
financially and operationally to move our critical work forward the moment the public health situation allows for that. Many of the patients we work with are battling devastating diseases that will not wait for this pandemic to pass.
Just prior to substantial market dislocation driven by COVID-19, BridgeBio strengthened its balance sheet by raising
$550 million in gross proceeds through the issuance of 2.50% Convertible Senior Notes due in 2027 (2027 Notes). This important financing added to approximately $700 million in gross proceeds raised from our initial public offering in June
2019 and Series D announced in January 2019, and puts BridgeBio in a strong financial position to execute on the 20+ drug development and discovery programs in its pipeline. The company expects current cash, cash equivalents and marketable
securities to carry it through critical and high-value milestones stretching into 2022.
Our recent financings have focused on solving for two objectives at once: securing the capital
required to independently advance our pipeline, while minimizing shareholder dilution, said BridgeBio CFO Brian Stephenson, Ph.D., CFA. One of the original goals in the founding of BridgeBio was to create a vehicle that could attract a
new set of investors to fund critical biomedical research and drug development by taking a sufficiently large number of shots on goal, within an advantaged research and development space, to build conviction that multiple approved products are not
just possible but statistically probable over time. We appreciate the confidence investors have demonstrated in the critical work we are doing for patients.
Steps BridgeBio has taken in response to COVID-19
First quarter 2020 and recent
Multiple new clinical studies are ready to initiate pending stabilization of
First quarter 2020 financial results:
equivalents and marketable securities
Cash, cash equivalents and marketable securities, excluding restricted cash, totaled $928.4 million as of
March 31, 2020 compared to $577.1 million at December 31, 2019. The net change in cash balance of $351.3 million reflects $537.6 million in net proceeds received from the issuance of our 2027 Notes, $24.1 million in net
proceeds received from Eidos at-the-market issuance of shares, offset by payment of $75.0 million to repurchase BridgeBio shares, $49.3 million payment
related to capped call option and the remaining payment of $86.1 million primarily related to operating expenses.
Operating expenses for the first quarter of 2020 were $102.5 million, as compared to $63.8 million for the same period in the prior year. The
increase in operating expenses of $38.7 million was attributable to the increase in external-related costs and increase in headcount to support the progression in our research and development programs, including our increasing research
pipelines, and overall growth of our operations.
We have experienced some delays in our research and development activities arising from delays in
enrollment of certain of our ongoing clinical trials and in the commencement of certain planned trials due to the global outbreak of COVID-19. The delays experienced occurred towards the end of the first
quarter of 2020 and therefore, our research and development expenses have not been significantly impacted for the full quarter. However, we believe that delays in our ongoing and planned clinical trials and adjustments to certain of our study
procedures, such as enabling alternative site, telehealth and home visits, at-home drug delivery, as well as mitigation strategies with our contract manufacturing organizations, may increase our expenses or
draw them out over a longer period of time. The longer term impact of COVID-19 on our operating expenses is currently unknown.
BRIDGEBIO PHARMA, INC.
Condensed Consolidated Statements of Operations
(in thousands, except shares and per share amounts)
| Three Months Ended March 31, | ||||||||
| 2020 | 2019 | |||||||
| (Unaudited) | ||||||||
| Operating expenses: | ||||||||
| Research and development | $ | 68,225 | $ | 44,853 | ||||
| General and administrative | 34,262 | 18,899 | ||||||
| Total operating expenses | 102,487 | 63,752 | ||||||
| Loss from operations | (102,487 | ) | (63,752 | ) | ||||
| Other income (expense), net: | ||||||||
| Interest income | 1,941 | 2,107 | ||||||
| Interest expense | (4,010 | ) | (1,671 | ) | ||||
| Share in net loss of equity method investment | (4,599 | ) | ||||||
| Other income (expense) | 474 | (1,521 | ) | |||||
| Total other income (expense), net | (1,595 | ) | (5,684 | ) | ||||
| Net loss | (104,082 | ) | (69,436 | ) | ||||
| Net loss attributable to redeemable convertible noncontrolling interests and noncontrolling interests | 12,232 | 8,251 | ||||||
| Net loss attributable to common stockholders of BridgeBio | $ | (91,850 | ) | $ | (61,185 | ) | ||
| Net loss per share, basic and diluted | $ | (0.78 | ) | $ | (0.66 | ) | ||
| Weighted-average shares used in computing net loss per share, basic and diluted | 117,803,438 | 92,330,072 |
BRIDGEBIO PHARMA, INC.
Condensed Consolidated Balance Sheets
| March 31, | December 31, | |||||||
| 2020 | 2019 | |||||||
| (Unaudited) | (1) | |||||||
| Assets | ||||||||
| Cash and cash equivalents and marketable securities (2) | $ | 928,385 | $ | 577,137 | ||||
| Prepaid expenses and other current assets | 19,782 | 22,629 | ||||||
| Property and equipment, net | 15,755 | 5,625 | ||||||
| Operating lease right-of-use assets, net | 8,855 | |||||||
| Other assets | 17,022 | 26,288 | ||||||
| Total assets | $ | 989,799 | $ | 631,679 | ||||
| Liabilities, Redeemable Convertible Noncontrolling Interests and Stockholders Equity | ||||||||
| Accounts payable | $ | 13,086 | $ | 8,852 | ||||
| Accrued liabilities | 45,779 | 39,455 | ||||||
| LEO call option liability | 3,539 | 4,078 | ||||||
| Operating lease liabilities | 11,188 | |||||||
| Build-to-suit lease obligation | 8,000 | |||||||
| Term loans | 92,416 | 91,791 | ||||||
| 2027 Notes | 368,923 | |||||||
| Other liabilities | 2,797 | 3,527 | ||||||
| Redeemable convertible noncontrolling interests | 3,053 | 2,243 | ||||||
| Total BridgeBio stockholders equity | 380,715 | 408,454 | ||||||
| Noncontrolling interests | 68,303 | 65,279 | ||||||
| Total liabilities, redeemable convertible noncontrolling interests and stockholders equity | $ | 989,799 | $ | 631,679 |
About BridgeBio Pharma
BridgeBio is a team of experienced drug discoverers, developers and innovators working to create life-altering medicines that target well-characterized genetic
diseases at their source. BridgeBio was founded in 2015 to identify and advance transformative medicines to treat patients who suffer from Mendelian diseases, which are diseases that arise from defects in a single gene, and cancers with clear
genetic drivers. BridgeBio s pipeline of over 20 development programs includes product candidates ranging from early discovery to late-stage development. For more information, visit bridgebio.com.
BridgeBio Pharma Forward-Looking Statements
release contains forward-looking statements. Statements we make 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, 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 and are making this statement for purposes of
complying with those safe harbor provisions. These forward-looking statements, including statements relating to expectations, plans and prospects regarding the preclinical and clinical development plans, clinical trial designs, clinical and
therapeutic potential, and strategy of BridgeBio s product candidates, including, but not limited to, the unknown future impact of the COVID-19 pandemic s delay to certain clinical trial milestones
and effect on BridgeBio s operations, the number of potential medicines in our portfolio, our plans to file an NDA for infigratinib in cholangiocarcinoma and multiple INDs for new product candidates in 2020, the initiation of our planned Phase
2/3 trial of Zuretinol, the availability of topline data from our Phase 1/2 study of BBP-589, the anticipated dosing of the first children in our Phase 2 dose-ranging study of infigratinib in achondroplasia,
the completion of enrollment in our ongoing Phase 3 study of BBP-265 in ATTR-CM, the initiation of our Phase 3 trial of BBP-265
in ATTR-PN, the completion of our rolling NDA submission to FDA for fosdenopterin, the timing of last patient last visit for topical patidegib gel for Gorlin syndrome and high-frequency basal cell carcinoma,
the availability of updated results for infigratinib and our plans for further clinical development of infigratinib in FGFR+ cancer, our expected runway for cash, cash equivalents and marketable securities, and the timing of these events, reflect
our current views about our plans, intentions, expectations, strategies and prospects, which are based on the information currently available to us and on assumptions we have made. Although we believe that our plans, intentions, expectations,
strategies and prospects 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, potential adverse impacts due to the global COVID-19 pandemic such as delays in regulatory review, manufacturing and supply chain interruptions, adverse effects on healthcare systems and disruption of the global economy and those risks set forth in the Risk
Factors section of our most recent quarterly or annual periodic report filed with the SEC and our other SEC filings. Moreover, BridgeBio operates in a very competitive and rapidly changing environment in which new risks emerge from time to time.
These forward-looking statements are based upon the current expectations and beliefs of BridgeBio s management as of the date of this 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.
Grace Rauh, BridgeBio Pharma
John Grimaldi, Burns McClellan
Source: BridgeBio Pharma