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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): November 4, 2024
UNITY BIOTECHNOLOGY, INC.
(Exact name of registrant as specified in its charter)
Delaware |
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001-38470 |
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26-4726035 |
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(State or other jurisdiction of incorporation) |
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(Commission File Number) |
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(IRS Employer Identification Number) |
285 East Grand Ave.
South San Francisco, CA 94080
(Address of principal executive offices, including Zip Code)
Registrant’s telephone number, including area code: (650) 416-1192
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 $0.0001 per share |
UBX |
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 November 4, 2024, Unity Biotechnology, Inc. (the “Company”) announced its financial results for the third quarter ended September 30, 2024. 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 this Current Report on Form 8-K, including the attached Exhibit 99.1, is being furnished and shall not be deemed to be “filed” for the purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that section, nor shall it be deemed to be incorporated by reference in any filing made by the Company under the Securities Act of 1933, as amended, or the Exchange Act, except as shall be expressly set forth by specific reference in such a filing.
Item 9.01 Financial Statements and Exhibits.
Reference is made to the Exhibit Index attached hereto.
EXHIBIT INDEX
Exhibit No. |
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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, as amended, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
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UNITY BIOTECHNOLOGY, INC. |
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Date: November 4, 2024 |
By: |
/s/ Anirvan Ghosh |
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Anirvan Ghosh, Ph.D. |
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Chief Executive Officer |
Exhibit 99.1
UNITY Biotechnology, Inc. Reports Third Quarter 2024 Financial Results
and Business Updates
SOUTH SAN FRANCISCO, Calif., November 4, 2024 (GLOBE NEWSWIRE) -- UNITY Biotechnology, Inc. (UNITY) [NASDAQ:UBX], a biotechnology company developing therapeutics to slow, halt, or reverse diseases of aging, today reported financial results for the third quarter ended September 30, 2024.
“As recently discussed on our Ophthalmology Day for investors and analysts, diabetic macular edema represents a large underserved market due to inadequate response to anti-VEGF standard of care, continued vision loss over time despite treatment, and high treatment burden leading to discontinuation,” said Anirvan Ghosh, Ph.D., chief executive officer of UNITY. “We believe that UBX1325 (foselutoclax) with its novel mechanism of action has the potential to improve long-term visual outcomes for DME patients, via a proven and safe intravitreal route of administration. We believe that the readouts from the Phase 2b ASPIRE study comparing UBX1325 to the aflibercept standard of care will provide a definitive dataset to inform the design of a potential pivotal study.”
In the third quarter of 2024, UNITY had a Type C interaction with the U.S. Food and Drug Administration, or FDA, regarding the development of UBX1325 (foselutoclax) for DME. Based on that interaction, UNITY expects that a pivotal study would need to be a non-inferiority trial comparing UBX1325 to an approved anti-VEGF agent such as aflibercept. The endpoint for regulatory approval is expected to be an assessment of best-corrected visual acuity (BCVA), as assessed by the ETDRS scale with a non-inferiority margin of 4 letters.
The webcast presentation from the Company’s Ophthalmology Investor and Analyst Day is available here.
UBX1325 (foselutoclax) is designed as a novel and durable therapeutic option in diabetic macular edema (DME) that acts via a senolytic mechanism of action, with the potential to address shortcomings of the current standard of care, such as high treatment burden and sub-optimal response to treatment.
UNITY expects topline 24-week primary endpoint data in the first quarter of 2025 and 36-week data in the second quarter of 2025. The Phase 2b ASPIRE study in DME is a multi-center, randomized, double-masked, active-controlled study designed to evaluate the safety and efficacy of UBX1325 in a head-to-head comparison to aflibercept. More information about ASPIRE (NCT06011798) can be found here.
Third Quarter Financial Results
Cash, cash equivalents and marketable securities totaled $29.0 million as of September 30, 2024 compared with $43.2 million as of December 31, 2023. UNITY believes that current cash, cash equivalents and marketable securities are sufficient to fund operations into the third quarter of 2025.
Net loss for the three months ended September 30, 2024 was $6.5 million compared to $14.8 million for the three months ended September 30, 2023. Cash used in operations during the first, second and third quarters of 2024 was $15.0 million compared to $29.5 million during the first, second, and third quarters of 2023.
Research and development expenses decreased by $1.8 million, to $2.8 million for three months ended September 30, 2024 from $4.6 million for the three months ended September 30, 2023. The decrease was primarily due to $0.9 million in personnel costs due to our reduced headcount related to our reduction in force, $0.8 million in direct research and development expenses mainly due to the completion of the Phase 2 BEHOLD study of UBX1325 in patients with DME and the Phase 2 ENVISION study of UBX1325 in patients with AMD, and $0.1 million in operating costs due to reduced fixed assets depreciation and reduced office space.
General and administrative expenses decreased by $0.5 million, to $3.8 million for the three months ended September 30, 2024 from $4.3 million for the three months ended September 30, 2023. The decrease was primarily due to decreases of $0.5 million in personnel-related expenses due to reduced headcount and the reduction in bonus and severance amounts paid as compared to 2023 and $0.1 million in operating costs mainly from the continuation of sublease income generated from the East Grand property, partially offset by an increase of $0.1 million in professional fees and accounting service fees.
About UNITY
UNITY is developing a new class of therapeutics to slow, halt, or reverse diseases of aging. UNITY’s current focus is on creating medicines to selectively eliminate or modulate senescent cells and thereby provide transformative benefit in age-related ophthalmologic and neurologic diseases. More information is available at www.unitybiotechnology.com or follow us on Twitter and LinkedIn.
Forward-Looking Statements
This press release contains forward-looking statements including statements related to UNITY’s understanding of cellular senescence and the role it plays in diseases of aging, the potential for UNITY to develop therapeutics to slow, halt, or reverse diseases of aging, including for ophthalmologic and neurologic diseases, the potential for UNITY to successfully commence and complete clinical studies of UBX1325 for DME, AMD, and other ophthalmologic diseases, the expected timing of enrollment and results of the clinical trials in UBX1325, and UNITY’s expectations regarding the sufficiency of its cash runway. These statements involve substantial known and unknown risks, uncertainties, and other factors that may cause our actual results, levels of activity, performance, or achievements to be materially different from the information expressed or implied by these forward-looking statements, including risks related to delay or disruption in the enrollment of patients in clinical trials, risks relating to the uncertainties inherent in the drug development process, and risks relating to UNITY’s understanding of senescence biology. We may not actually achieve the plans, intentions, or expectations disclosed in our forward-looking statements, and you should not place undue reliance on our forward-looking statements. Actual results or events could differ materially from the plans, intentions and expectations disclosed in the forward-looking statements we make. The forward-looking statements in this press release represent our views as of the date of this release. We anticipate that subsequent events and developments will cause our views to change. However, while we may elect to update these forward-looking statements at some point in the future, we have no current intention of doing so except to the extent required by applicable law. You should, therefore, not rely on these forward-looking statements as representing our views as of any date subsequent to the date of this release. For a further description of the risks and uncertainties that could cause actual results to differ from those expressed in these forward-looking statements, as well as risks relating to the business of the Company in general, see UNITY’s most recent Quarterly Report on Form 10-Q for the quarter ended September 30, 2024, filed with the Securities and Exchange Commission on November 4, 2024, as well as other documents that may be filed by UNITY from time to time with the Securities and Exchange Commission.
Unity Biotechnology, Inc.
Statements of Operations and Comprehensive Loss
(In thousands, except share and per share amounts)
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Three Months Ended |
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Nine Months Ended |
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September 30, |
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September 30, |
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||||||||||
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2024 |
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2023 |
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2024 |
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2023 |
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(Unaudited) |
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(Unaudited) |
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Operating expenses: |
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Research and development |
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$ |
2,787 |
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$ |
4,632 |
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$ |
9,971 |
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$ |
16,828 |
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General and administrative |
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3,815 |
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4,347 |
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11,209 |
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14,560 |
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Impairment of long-lived assets |
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— |
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5,602 |
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— |
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5,602 |
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Total operating expenses |
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6,602 |
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14,581 |
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|
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21,180 |
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|
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36,990 |
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Loss from operations |
|
|
(6,602 |
) |
|
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(14,581 |
) |
|
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(21,180 |
) |
|
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(36,990 |
) |
Interest income |
|
|
396 |
|
|
|
689 |
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|
|
1,424 |
|
|
|
2,349 |
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Interest expense |
|
|
— |
|
|
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(566 |
) |
|
|
— |
|
|
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(2,451 |
) |
Gain (loss) on warrant liability |
|
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(215 |
) |
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253 |
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|
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2,407 |
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|
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2,283 |
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Other income (expense), net |
|
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(60 |
) |
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(577 |
) |
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(201 |
) |
|
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(711 |
) |
Net loss |
|
|
(6,481 |
) |
|
|
(14,782 |
) |
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(17,550 |
) |
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(35,520 |
) |
Other comprehensive gain (loss) |
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|
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|
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||||
Unrealized gain (loss) on marketable debt securities |
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74 |
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|
81 |
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63 |
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|
|
196 |
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Comprehensive loss |
|
$ |
(6,407 |
) |
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$ |
(14,701 |
) |
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$ |
(17,487 |
) |
|
$ |
(35,324 |
) |
Net loss per share, basic and diluted |
|
$ |
(0.38 |
) |
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$ |
(1.01 |
) |
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$ |
(1.04 |
) |
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$ |
(2.46 |
) |
Weighted-average number of shares used in |
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16,849,283 |
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14,598,218 |
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16,816,706 |
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14,446,672 |
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Unity Biotechnology, Inc.
Condensed Balance Sheets
(In thousands)
|
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September 30, |
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December 31, |
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2024 |
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2023 |
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(Unaudited) |
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Assets |
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Current Assets: |
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Cash and cash equivalents |
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$ |
8,898 |
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$ |
19,803 |
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Short-term marketable securities |
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20,139 |
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23,398 |
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Prepaid expenses and other current assets |
|
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1,226 |
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|
3,404 |
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Total current assets |
|
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30,263 |
|
|
|
46,605 |
|
Property and equipment, net |
|
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4,414 |
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|
|
5,082 |
|
Operating lease right-of-use assets |
|
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11,359 |
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|
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12,981 |
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Long-term restricted cash |
|
|
896 |
|
|
|
896 |
|
Other long-term assets |
|
|
200 |
|
|
|
126 |
|
Total assets |
|
$ |
47,132 |
|
|
$ |
65,690 |
|
Liabilities and Stockholders’ Equity |
|
|
|
|
|
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||
Current liabilities: |
|
|
|
|
|
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Accounts payable |
|
$ |
1,804 |
|
|
$ |
1,380 |
|
Accrued compensation |
|
|
1,704 |
|
|
|
1,841 |
|
Accrued and other current liabilities |
|
|
5,276 |
|
|
|
4,619 |
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Total current liabilities |
|
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8,784 |
|
|
|
7,840 |
|
Operating lease liability, net of current portion |
|
|
20,698 |
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|
|
23,539 |
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Warrant liability |
|
|
3,506 |
|
|
|
5,913 |
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Total liabilities |
|
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32,988 |
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|
|
37,292 |
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Commitments and contingencies |
|
|
|
|
|
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||
Stockholders’ equity: |
|
|
|
|
|
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||
Common stock |
|
|
2 |
|
|
|
2 |
|
Additional paid-in capital |
|
|
516,006 |
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|
|
512,773 |
|
Accumulated other comprehensive gain |
|
|
39 |
|
|
|
(24 |
) |
Accumulated deficit |
|
|
(501,903 |
) |
|
|
(484,353 |
) |
Total stockholders’ equity |
|
|
14,144 |
|
|
|
28,398 |
|
Total liabilities and stockholders’ equity |
|
$ |
47,132 |
|
|
$ |
65,690 |
|
Media
Inizio Evoke Comms
Katherine Smith
katherine.smith@inizioevoke.com
Investor Contact
LifeSci Advisors, LLC
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jallaire@lifesciadvisors.com