EX-99.1 2 d280542dex991.htm EX-99.1 EX-99.1

Exhibit 99.1

 

LOGO

INOVIO Reports Financial Results and Highlights for the Third Quarter 2022

 

   

Announced positive interim data for INO-3107 as a potential first-in-class treatment for Recurrent Respiratory Papillomatosis

 

   

Advanced strategy to focus on developing candidates that have the greatest opportunity for near-term success

 

   

Updates prior financial guidance and extends cash runway into first quarter of 2025

 

   

Company will hold investor call today at 4:30 PM ET

PLYMOUTH MEETING, PA – November 8, 2022 – INOVIO (NASDAQ:INO), a biotechnology company focused on developing and commercializing DNA medicines to help treat and prevent infectious diseases, cancer, and diseases associated with HPV, today reported financial results for the quarter and nine months ended September 30, 2022. INOVIO’s management will host a live conference call and webcast at 4:30 p.m. Eastern Time today to discuss financial results and provide a general business update for the third quarter. The live webcast and replay may be accessed by visiting INOVIO’s website at http://ir.inovio.com/events-and-presentations/default.aspx.

Dr. Jacqueline Shea, INOVIO’s President and Chief Executive Officer, said, “INOVIO continues to implement its strategy of delivering the potential of DNA medicines to patients, focusing its resources on those candidates that have the greatest opportunity for near-term success. In the third quarter, INOVIO announced positive Phase 1/2 data for INO-3107, a promising DNA medicine candidate as a potential treatment for recurrent respiratory papillomatosis. These results are exciting to us because they build upon our ongoing work indicating that DNA medicines have the potential to treat HPV-associated diseases. We are also encouraged by other candidates in our pipeline, such as INO-5401, which has also shown positive results this year as a potential treatment for glioblastoma. We look forward to continuing to advance these programs as well as other pipeline programs for which we continue to anticipate data announcements in the coming months.”

Dr. Shea continued: “In the third quarter, we also continued our efforts to create a more focused company rooted in operational excellence and optimized capital and resource allocation. Our decision to discontinue our internally funded development of INO-4800 as a heterologous COVID-19 booster is in line with this strategy and we will deploy cost savings from this effort to the development of other promising candidates. We will also leverage the strengths and capabilities developed by our COVID-19 program across our portfolio, where appropriate, such as our new intradermal 3PSP investigational delivery device.”


Recent Corporate Highlights

Positive Phase 1/2 Trial Results INO-3107 – In the third quarter, INOVIO announced positive interim Phase 1/2 results for INO-3107 in participants with recurrent respiratory papillomatosis (RRP). In the open-label, multicenter trial (NCT:04398433), INO-3107 demonstrated statistical significance based on the clinical endpoint of a reduction in the number of RRP surgical interventions in the year following administration of INO-3107 compared with the year prior to treatment, in an initial cohort of 21 participants. In the trial, there was a median decrease of three (3) surgical interventions. (95% confidence interval 1, 3). In addition, 16 of 21 (76%) participants in the trial experienced a decrease in the number of surgical interventions in the year following administration of INO-3107 relative to the number of surgeries in the year prior to the trial. Of those 16 participants, six (29%) required no surgical intervention during the 52-week trial period.

In the trial, treatment with INO-3107 induced cellular responses against both HPV 6 and HPV 11, inducing both CD4 and CD8 T cells. T-cell responses were still observed at Week 52, indicating a persistent cellular memory response.

INO-3107 demonstrated a favorable safety and tolerability profile in the trial. Results from the second cohort of 11 participants are expected in the first half of 2023.

Internally Funded Development of INO-4800 Heterologous Boost Trials Discontinued – In October, INOVIO announced that following a comprehensive review of its portfolio, market conditions, and global demand for COVID-19 vaccines, it had discontinued internally-funded efforts to develop INO-4800 as a COVID-19 heterologous booster vaccine. INOVIO’s efforts towards the global COVID-19 pandemic response will continue through its participation in the Solidarity Trial Vaccines (STV) sponsored by the World Health Organization (WHO) and its preclinical work on a pan-COVID vaccine candidate. In addition, INOVIO’s partner Advaccine will continue to develop INO-4800 as a heterologous booster vaccine using its own resources. Future updates related to this trial will be provided by Advaccine.

Third Quarter 2022 Financial Results

As of September 30, 2022, cash and cash equivalents and short-term investments were $281.9 million compared to $401.3 million as of December 31, 2021. As of September 30, 2022, INOVIO had 249.5 million common shares outstanding and 268.7 million common shares outstanding on a fully diluted basis, after giving effect to the exercise, vesting, and conversion, as applicable, of its outstanding options, restricted stock units, convertible preferred stock, and convertible debt.

INOVIO reported total revenue of $9.2 million for the three months ended, September 30, 2022, compared to $292,000 for the same period in 2021. The increase in revenue resulted from the fulfillment of obligations under its contract with the U.S. Department of Defense. Total operating expenses were $44.9 million compared to $60.2 million for the same period in 2021.

INOVIO’s net loss for the quarter ended September 30, 2022, was $37.8 million, or $0.15 per basic and diluted share, compared to net loss of $60.2 million, or $0.29 per basic and diluted share, for the quarter ended September 30, 2021.


Operating Expenses

Research and development (R&D) expenses for the three months ended September 30, 2022, were $33.1 million compared to $47.1 million for the same period in 2021. The decrease in R&D expenses was primarily related to lower drug manufacturing, outside services and clinical study expenses related to INO-4800 and VGX-3100, and lower engineering services and expensed equipment related to our CELLECTRA® 3PSP device array automation project. These decreases were offset by $8.2 million lower contra-research and development expenses recorded from grant agreements, among other variances.

General and administrative (G&A) expenses were $11.8 million for the three months ended September 30, 2022, versus $13.2 million for the same period in 2021. The decrease in G&A expenses was primarily related to a decrease in employee and consultant non-cash stock-based compensation, among other variances.

INOVIO’s balance sheet and statement of operations are provided below. Additional information is included in INOVIO’s quarterly report on Form 10-Q for the quarter ended September 30, 2022, which can be accessed at: http://ir.inovio.com/financials/default.aspx.

Financial Guidance

INOVIO is updating its prior guidance and now expects its cash runway to extend into the first quarter of 2025. This projection includes its cash burn estimate of approximately $45 million for the fourth quarter of 2022 and its ongoing expectation that cash burn will decrease incrementally from there into the first quarter of 2025. These projections do not include any funds that may be raised through the Company’s existing at-the-market program or other capital-raising activities.

Conference Call / Webcast Information

INOVIO’s management will host a live conference call and webcast at 4:30 p.m. ET today to discuss INOVIO’s financial results and provide a general business update. The live webcast and replay may be accessed by visiting INOVIO’s website at http://ir.inovio.com/events-and-presentations/default.aspx.

About INOVIO

INOVIO is a biotechnology company focused on developing and commercializing DNA medicines to help treat and protect people from infectious diseases, cancer, and diseases associated with HPV. INOVIO’s DNA medicines in development are delivered using its investigational proprietary smart device to produce immune responses against targeted pathogens and cancers.

For more information, visit www.inovio.com.

About CELLECTRA® Delivery Technology

INOVIO’s DNA medicines are delivered into cells either intramuscularly (IM) or intradermally (ID) using its investigational proprietary CELLECTRA smart devices. CELLECTRA devices use brief (millisecond-long) electrical pulses to reversibly create tiny pores in the cell membrane, which enhance cellular uptake of DNA medicines. In 2022, with the support of the U.S. Department of Defense, INOVIO developed its next-generation ID delivery device, 3PSP, and an automated high throughput array manufacturing process.

Contacts

Investors & Media:

Gene Kim, (267) 589-9471, gene.kim@inovio.com

Thomas Hong, (267) 440-4298, thomas.hong@inovio.com


Forward-Looking Statements

This press release contains certain forward-looking statements relating to our business, including our plans to develop and commercialize DNA medicines and our expectations regarding our research and development programs, including the planned initiation and conduct of pre-clinical studies and clinical trials and the availability and timing of data from those studies and trials, and expectations with respect to our cash resources and expected operating expenses into first quarter of 2025. Actual events or results may differ from the expectations set forth herein as a result of a number of factors, including uncertainties inherent in pre-clinical studies, clinical trials, product development programs and commercialization activities and outcomes, the availability of funding to support continuing research and studies in an effort to prove safety and efficacy of electroporation technology as a delivery mechanism or develop viable DNA medicines, our ability to support our pipeline of DNA medicine products, the ability of our collaborators to attain development and commercial milestones for products we license and product sales that will enable us to receive future payments and royalties, the adequacy of our capital resources, the availability or potential availability of alternative therapies or treatments for the conditions targeted by us or collaborators, including alternatives that may be more efficacious or cost effective than any therapy or treatment that we and our collaborators hope to develop, issues involving product liability, issues involving patents and whether they or licenses to them will provide us with meaningful protection from others using the covered technologies, whether such proprietary rights are enforceable or defensible or infringe or allegedly infringe on rights of others or can withstand claims of invalidity and whether we can finance or devote other significant resources that may be necessary to prosecute, protect or defend them, the level of corporate expenditures, assessments of our technology by potential corporate or other partners or collaborators, capital market conditions, the impact of government healthcare proposals and other factors set forth in our Annual Report on Form 10-K for the year ended December 31, 2021, our Quarterly Report on Form 10-Q for the quarter ended September 30, 2022, and other filings we make from time to time with the Securities and Exchange Commission. There can be no assurance that any product candidate in our pipeline will be successfully developed, manufactured, or commercialized, that the results of clinical trials will be supportive of regulatory approvals required to market products, or that any of the forward-looking information provided herein will be proven accurate. Forward-looking statements speak only as of the date of this release, and we undertake no obligation to update or revise these statements, except as may be required by law.


INOVIO Pharmaceuticals, Inc.

CONDENSED CONSOLIDATED BALANCE SHEETS

 

     September 30,
2022
    December 31,
2021
 
ASSETS     

Current assets:

    

Cash and cash equivalents

   $ 21,988,239     $ 71,143,778  

Short-term investments

     259,894,898       330,170,940  

Accounts receivable

     2,442,866       5,466,850  

Accounts receivable from affiliated entities

     7,637,820       2,565,194  

Prepaid expenses and other current assets

     57,970,979       38,836,991  

Prepaid expenses and other current assets from affiliated entities

     273,211       261,192  
  

 

 

   

 

 

 

Total current assets

     350,208,013       448,444,945  

Fixed assets, net

     15,588,103       17,453,206  

Investment in affiliated entity

     2,129,992       3,906,796  

Intangible assets, net

     2,249,444       2,626,355  

Goodwill

     10,513,371       10,513,371  

Operating lease right-of-use assets

     10,577,077       11,571,026  

Other assets

     701,986       1,425,794  
  

 

 

   

 

 

 

Total assets

   $ 391,967,986     $ 495,941,493  
  

 

 

   

 

 

 
LIABILITIES AND STOCKHOLDERS’ EQUITY     

Current liabilities:

    

Accounts payable and accrued expenses

   $ 74,147,792     $ 47,644,530  

Accounts payable and accrued expenses due to affiliated entities

     1,633,788       548,032  

Accrued clinical trial expenses

     13,485,846       10,326,266  

Deferred revenue

     —         21,628  

Operating lease liability

     2,820,862       2,603,956  

Grant funding liability

     2,709,953       4,559,721  

Grant funding liability from affiliated entity

     116,500       37,500  
  

 

 

   

 

 

 

Total current liabilities

     94,914,741       65,741,633  

Deferred revenue, net of current portion

     —         64,361  

Convertible senior notes

     16,301,352       14,959,647  

Operating lease liability, net of current portion

     13,312,383       15,459,559  

Deferred tax liabilities

     32,046       32,046  

Other liabilities

     710,348       14,826  
  

 

 

   

 

 

 

Total liabilities

     125,270,870       96,272,072  
  

 

 

   

 

 

 

Stockholders’ equity:

    

Preferred stock

     —         —    

Common stock

     249,484       217,382  

Additional paid-in capital

     1,700,717,489       1,609,589,797  

Accumulated deficit

     (1,433,384,645     (1,209,855,522

Accumulated other comprehensive loss

     (885,212     (282,236
  

 

 

   

 

 

 

Total Inovio Pharmaceuticals, Inc. stockholders’ equity

     266,697,116       399,669,421  
  

 

 

   

 

 

 

Total liabilities and stockholders’ equity

   $ 391,967,986     $ 495,941,493  
  

 

 

   

 

 

 


INOVIO Pharmaceuticals, Inc.

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS

(Unaudited)

 

     Three Months Ended
September 30,
    Nine Months Ended
September 30,
 
     2022     2021     2022     2021  

Revenue from collaborative arrangements and other contracts

   $ 9,154,133     $ 291,698     $ 10,137,602     $ 935,643  
  

 

 

   

 

 

   

 

 

   

 

 

 

Operating expenses:

        

Research and development

     33,087,130       47,088,669       145,530,626       156,941,505  

General and administrative

     11,824,047       13,156,183       76,234,341       39,703,718  
  

 

 

   

 

 

   

 

 

   

 

 

 

Total operating expenses

     44,911,177       60,244,852       221,764,967       196,645,223  
  

 

 

   

 

 

   

 

 

   

 

 

 

Loss from operations

     (35,757,044     (59,953,154     (211,627,365     (195,709,580

Other income (expense):

        

Interest income

     1,365,759       766,271       2,893,240       2,463,618  

Interest expense

     (313,488     (476,374     (940,464     (1,456,134

Loss on investment in affiliated entities

     (305,061     (21,999     (1,776,804     (573,656

Net unrealized loss on available-for-sale equity securities

     (1,833,284     (455,299     (10,641,026     (1,166,764

Other (expense) income, net

     (940,778     (28,486     (1,097,294     165,773  
  

 

 

   

 

 

   

 

 

   

 

 

 

Net loss before share in net loss of Geneos

     (37,783,896     (60,169,041     (223,189,713     (196,276,743

Share in net loss of Geneos

     —         —         (2,165,213     (434,387
  

 

 

   

 

 

   

 

 

   

 

 

 

Net loss

   $ (37,783,896   $ (60,169,041   $ (225,354,926   $ (196,711,130
  

 

 

   

 

 

   

 

 

   

 

 

 

Net loss per share

        

Basic and diluted

   $ (0.15   $ (0.29   $ (0.96   $ (0.95
  

 

 

   

 

 

   

 

 

   

 

 

 

Weighted average number of common shares outstanding

        

Basic and diluted

     249,351,023       210,304,836       234,634,724       207,455,684