8-K
false 0001888012 0001888012 2022-08-10 2022-08-10

 

 

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 10, 2022

 

 

HilleVax, Inc.

(Exact name of registrant as specified in its charter)

 

 

 

Delaware   001-41365   85-0545060

(State or other jurisdiction

of incorporation)

 

(Commission

File Number)

 

(I.R.S. Employer

Identification No.)

75 State Street, Suite 100 - #9995

Boston, Massachusetts

  02109
(Address of principal executive offices)   (Zip Code)

(617) 213-5054

(Registrant’s telephone number, including area code)

(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, $0.0001 par value per share   HLVX   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 (Sec.230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (Sec.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 10, 2022, HilleVax, Inc. (the “Company”) issued a press release announcing its financial results for the quarter ended June 30, 2022. A copy of the press release is attached hereto as Exhibit 99.1 and is incorporated herein by reference.

In accordance with General Instruction B.2 of Form 8-K, the information in this Current Report on 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 (the “Exchange Act”), or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference in any filing under the Securities Act of 1933, as amended, or the Exchange Act, whether made before or after the date hereof, except as expressly set forth by specific reference in such filing.

Item 9.01. Financial Statements and Exhibits.

(d) Exhibits

 

Exhibit
No.
  

Description

99.1    Press Release issued on August 10, 2022
104    Cover Page Interactive Data File (embedded within the Inline XBRL document)

 


SIGNATURE

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.

 

    HilleVax, Inc.
Date: August 10, 2022     By:  

/s/ David Socks

    Name:   David Socks
    Title:   Chief Financial Officer and Chief Business Officer
EX-99.1

Exhibit 99.1

 

LOGO

HilleVax Reports Second Quarter 2022 Financial Results and Highlights Recent Company Progress

BOSTON, August 10, 2022 – HilleVax, Inc. (Nasdaq: HLVX), a clinical-stage biopharmaceutical company focused on developing and commercializing novel vaccines, today reported financial results for the quarter ended June 30, 2022, highlighted recent program progress, and outlined key upcoming milestones for HIL-214, the company’s investigational virus-like particle (VLP) based vaccine for the prevention of moderate-to-severe norovirus-related acute gastroenteritis.

“We recently reported the completion of enrollment of the prespecified 200 subject run-in for NOR-212, our Phase 2b field efficacy study of HIL-214 in infants. We now look forward to resuming enrollment in NOR-212 following the prespecified data monitoring committee safety assessment expected later this quarter,” said Rob Hershberg, MD, PhD, Chairman and Chief Executive Officer of HilleVax. “We are pleased that we remain on track with regards to achieving our key corporate milestones.”

Second Quarter 2022 and Recent Business Highlights

Financial and Corporate

 

   

In July 2022, HilleVax announced results from 5-year Phase 2 follow-up clinical trial supporting long-term immunogenicity of HIL-214.

 

   

In May 2022, HilleVax commenced NOR-212 and completed enrollment of the prespecified 200 subject run-in.

 

   

In May 2022, HilleVax completed its IPO, raising $230 million in aggregate gross proceeds, before deducting underwriting discounts and commissions and offering expenses, and began trading on The Nasdaq Global Select Market.

 

   

In April 2022, HilleVax entered into a Loan and Security Agreement with Hercules Capital, Inc. providing for term loans of up to $75 million in the aggregate, of which $5 million has been borrowed.

Upcoming Expected Milestones

 

   

NOR-212 interim safety results from the first 200 subjects in the third quarter of 2022

 

   

NOR-212 interim immunogenicity results from the first 200 subjects in the first half of 2023

 

   

NOR-212 topline safety and clinical efficacy data in the second half of 2023


Second Quarter 2022 Financial Results

As of June 30, 2022, the company had cash and cash equivalents totaling $314.6 million.

Research and development expenses for the second quarter 2022 were $8.8 million, compared to $0.5 million for the second quarter 2021.

General and administrative expenses for the second quarter 2022 were $4.0 million, compared to $0.8 million for the second quarter 2021.

Other expenses for the second quarter 2022 were $41.1 million, compared to $0.5 million for the second quarter 2021. The increase in other expenses was primarily driven by changes in the fair value of convertible promissory notes and warrant liabilities.

Net loss for the second quarter 2022 was $53.9 million, compared to $1.7 million for the second quarter 2021.

About HilleVax

HilleVax is a clinical-stage biopharmaceutical company focused on developing and commercializing novel vaccines. Its initial program, HIL-214, is a virus-like particle (VLP) based vaccine candidate in development for the prevention of moderate-to-severe acute gastroenteritis (AGE) caused by norovirus infection. Globally, norovirus is estimated to result in over approximately 700 million cases of AGE and 200,000 deaths per year, resulting in over $4 billion in direct health system costs and $60 billion in societal costs per year. The burden of norovirus falls disproportionately on young children and older adults. For more information about HilleVax, visit the company’s website at http://www.HilleVax.com.

Forward-Looking Statements

HilleVax cautions you that statements contained in this press release regarding matters that are not historical facts are forward-looking statements. The forward-looking statements are based on our current beliefs and expectations and include, but are not limited to: the expected continuation of enrollment in the NOR-212 trial based on the prespecified safety assessment and the expected timing of data readouts from this trial. Actual results may differ from those set forth in this press release due to the risks and uncertainties inherent in our business, including, without limitation: we currently depend entirely on the success of HIL-214, and we have not yet completed any clinical trials of HIL-214; potential delays in the commencement, enrollment, and completion of clinical trials and preclinical studies, including if the prespecified safety assessment by the clinical trial’s data monitoring committee is unfavorable; our dependence on third parties in connection with manufacturing, research and clinical and preclinical testing; unexpected adverse side effects or inadequate immunogenicity or efficacy of HIL-214 or any future vaccine candidates that may limit their development, regulatory approval, and/or commercialization; unfavorable results from clinical trials; results from prior clinical trials and studies not necessarily being predictive of future results; our ability to maintain undisrupted business operations due to the COVID-19 pandemic, including delaying or disrupting our clinical trials, manufacturing and supply chain; regulatory developments in the United States and foreign countries; any future impacts to our business resulting from the conflict between Russia and Ukraine or other geopolitical developments outside our control; our reliance on intellectual property rights under our license agreement with Takeda Vaccines, Inc.; our ability to obtain, maintain and enforce intellectual property protection for our vaccine candidates; we may use our capital resources sooner than we expect; and other risks described in our prior press releases and our filings with the Securities and Exchange Commission (SEC), including under the heading “Risk Factors” in our quarterly report on Form 10-Q and any subsequent filings with the SEC. You are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof, and we undertake no obligation to update such statements to reflect events that occur or circumstances that exist after the date hereof. All forward-looking statements are qualified in their entirety by this cautionary statement, which is made under the safe harbor provisions of the Private Securities Litigation Reform Act of 1995.

Contact:

David Socks

IR@hillevax.com

+1-617-213-5054


HilleVax, Inc.

Condensed Consolidated Statement of Operations Data

(in thousands, except share and per share data)

(unaudited)

 

     Three Months Ended
June 30,
    Six Months Ended
June 30,
 
     2022     2021     2022     2021  

Operating expenses:

        

Research and development

   $ 8,826     $ 460     $ 15,037     $ 727  

In-process research and development

     —         —         2,500       —    

General and administrative

     3,982       753       6,585       1,951  
  

 

 

   

 

 

   

 

 

   

 

 

 

Total operating expenses

     12,808       1,213       24,122       2,678  
  

 

 

   

 

 

   

 

 

   

 

 

 

Loss from operations

     (12,808     (1,213     (24,122     (2,678

Total other income (expense)

     (41,121     (454     (97,694     (535
  

 

 

   

 

 

   

 

 

   

 

 

 

Net loss

   $ (53,929   $ (1,667   $ (121,816   $ (3,213
  

 

 

   

 

 

   

 

 

   

 

 

 

Net loss per share, basic and diluted

   $ (2.03   $ (0.34   $ (7.30   $ (0.66
  

 

 

   

 

 

   

 

 

   

 

 

 

Weighted-average shares of common stock outstanding, basic and diluted

     26,512,881       4,935,738       16,685,372       4,869,690  
  

 

 

   

 

 

   

 

 

   

 

 

 


HilleVax, Inc.

Condensed Consolidated Balance Sheet Data

(in thousands)

(unaudited)

 

     June 30,
2022
       December 31,
2021
 

Cash and cash equivalents

   $ 314,612        $ 124,566  

Total assets

     341,232          127,159  

Total liabilities

     38,078          227,916  

Total stockholders’ equity (deficit)

     303,154          (100,757

Total liabilities and stockholders’ equity (deficit)

     341,232          127,159