Immunome Reports Fourth Quarter and Full Year 2021 Financial Results
Immunome, Inc. (Nasdaq: IMNM) has received a safe-to-proceed notification from the U.S. FDA for its IMM-BCP-01 investigational new drug application, allowing progress towards a Phase 1b clinical trial. The company’s antibody cocktail has shown promising in vitro efficacy against the Omicron variant of COVID-19, neutralizing it with significantly higher potency than existing treatments. Financially, Immunome reported a net loss of $7.9M for Q4 2021, with cash reserves of $49.2M as of December 31, 2021. Ongoing projects include the development of IMM-ONC-01 for targeting IL-38 in oncology.
- Received FDA safe-to-proceed notification for IMM-BCP-01.
- In vitro testing shows strong efficacy of IMM-BCP-01 against SARS-CoV-2 Omicron variant.
- Cash and cash equivalents of $49.2M provide stability for ongoing projects.
- Net loss of $7.9M for Q4 2021.
- Net loss attributable to common stockholders was $24.7M for the full year 2021.
- Immunome Receives Safe-to-Proceed Notification from
- Immunome Continues to Progress IMM-BCP-01 Towards Phase 1b Clinical Trial -
- Ongoing Progress on Oncology Pipeline, Including Lead Program Targeting IL-38, a Novel Innate Immunome Checkpoint -
“There remains a clear need for safe and efficacious antibody treatments against COVID-19, especially those less susceptible to mutational drift. We believe our three-antibody cocktail, IMM-BCP-01, has strong potential to address that unmet need. We are pleased the FDA has given us a safe-to-proceed notification and lifted the clinical hold for our Investigational New Drug (IND) application,” stated
“Additionally, we continue to progress IMM-ONC-01, our novel, IL-38-targeting innate immune checkpoint inhibitor, towards an IND submission in the second half of 2022,” Sarma continued. “Our preclinical work is ongoing, and we have analyzed IL-38 expression across nearly 60 tumor subtypes and we have confirmed a high frequency of expression in difficult to treat cancers, such as head and neck squamous cell carcinoma, gastroesophageal squamous carcinoma, and squamous lung carcinoma.”
Fourth Quarter and Subsequent Highlights
-
Demonstrated In Vitro Efficacy of IMM-BCP-01 Against SARS-CoV-2 Omicron Variant in Live Virus Testing. In
February 2022 ,Immunome announced that IMM-BCP-01 demonstrated effective neutralization of the Omicron variant of COVID-19 in in vitro testing. The combination of two antibodies in Immunome’s antibody cocktail, IMM20253/IMM20184, demonstrated neutralization of the Omicron variant within 3.5-fold potency compared to a preclinical version of sotrovimab in a head-to-head test using live virus samples. Additionally, IMM20253 exhibited a novel mechanism of action not reported in any other EUA antibodies by promoting a proteolytic cleavage of the portion of the spike protein needed for ACE2 binding.
-
IMM-BCP-01 IND Application for the Treatment of COVID-19. In
March 2022 , the FDA communicated that the clinical study can be initiated for our antibody cocktail for the treatment of SARS-CoV-2 following a brief clinical hold.Immunome is continuing its ongoing clinical preparations ahead of the Phase 1b trial.
This investigational work was funded by the
Financial Highlights
-
Cash and cash equivalents: As of
December 31, 2021 , cash and cash equivalents totaled .$49.2M -
Research and development (R&D) expenses: R&D expenses for the three months ended
December 31, 2021 were . R&D expenses for the year ended$4.4M December 31, 2021 were .$14.1M -
General and administrative (G&A) expenses: G&A expenses for the three months ended
December 31, 2021 were . G&A expenses for the year ended$3.5M December 31, 2021 were .$10.6M -
Net loss: Net loss attributable to common stockholders was
, or$7.9M $.65 per share, for the three months endedDecember 31, 2021 . Net loss attributable to common stockholders was , or$24.7M per share, for the year ended$2.14 December 31, 2021 . -
As of
December 31, 2021 ,Immunome has 12,110,373 shares of common stock outstanding.
About
Forward-Looking Statements
This press release includes certain disclosures that contain “forward-looking statements” intended to qualify for the “safe harbor” from liability established by the Private Securities Litigation Reform Act of 1995, as amended, including, without limitation, express or implied statements regarding Immunome’s beliefs and expectations regarding the advancement of its platform and programs, execution of its regulatory, research, clinical and strategic plans and anticipated upcoming milestones for its platform and programs, including expectations regarding, among other things, the timing and results of its preclinical studies and clinical trials, clinical plans, general regulatory actions, the translation of preclinical data into clinical safety and efficacy, the therapeutic potential and benefits of our product candidates, the possible need and demand for its product candidates and other statements that are not historical fact. Forward-looking statements may be identified by the words “anticipate,” “believe,” “estimate,” “expect,” “intend,” “plan,” “project,” “suggest,” “may,” “will,” “could,” “should,” “seek,” “potential” and similar expressions. Forward-looking statements are based on Immunome’s current expectations and are subject to inherent uncertainties, risks and assumptions that are difficult to predict. Factors that could cause actual results to differ include, but are not limited to, those risks and uncertainties associated with: the impact of the COVID-19 pandemic on Immunome’s business, operations, strategy, goals and anticipated milestones; the fact that research and development data are subject to differing interpretations and assessments; Immunome’s ability to execute on its strategy, including with respect to its R&D efforts, IND submissions and other regulatory filings, timing of these filings and the timing and nature of governmental authority feedback regarding the same, initiation and completion of any clinical studies, confirmatory testing and other anticipated milestones as and when anticipated; the effectiveness of Immunome’s product candidates, including the possibility that further preclinical data and any clinical trial data may be inconsistent with the data used for advancing the product candidates and that further variants of concern could emerge; Immunome’s ability to fund operations and raise capital; Immunome’s reliance on vendors; the competitive landscape; and the additional risks and uncertainties set forth more fully under the caption “Risk Factors” in Immunome’s Annual Report on Form 10-K filed with the
Condensed Statement of Operations | ||||||||
(in thousands, except share and per share amounts) | ||||||||
Year ended |
||||||||
2021 |
|
2020 |
||||||
Operating expenses: | ||||||||
Research and development | $ | 14,110 |
|
$ | 7,486 |
|
||
General and administrative | 11,094 |
|
4,775 |
|
||||
Total operating expenses | 25,204 |
|
12,261 |
|
||||
Loss from operations | (25,204 |
) |
(12,261 |
) |
||||
Other income (expenses): | ||||||||
Change in fair value of warrant liability | — |
|
(5,538 |
) |
||||
Other income | 503 |
|
— |
|
||||
Interest expense, net | (10 |
) |
(38 |
) |
||||
Total other expenses | 493 |
|
(5,576 |
) |
||||
Net loss | $ | (24,711 |
) |
$ | (17,837 |
) |
||
Per share information: | ||||||||
Net loss per common share, basic and diluted | $ | (2.14 |
) |
$ | (5.26 |
) |
||
Weighted-average common shares outstanding, basic and diluted | 11,538,668 |
|
3,389,592 |
|
Condensed Balance Sheets | ||||||||
(in thousands, except share and per share amounts) | ||||||||
|
||||||||
2021 |
|
2020 |
||||||
Assets | ||||||||
Current assets: | ||||||||
Cash and cash equivalents | $ | 49,229 |
|
$ | 39,766 |
|
||
Prepaid expenses and other current assets | 7,409 |
|
3,128 |
|
||||
Total current assets | 56,638 |
|
42,894 |
|
||||
Property and equipment, net | 855 |
|
1,531 |
|
||||
Restricted cash | 100 |
|
100 |
|
||||
Deferred offering costs | 332 |
|
- |
|
||||
Total assets | $ | 57,925 |
|
$ | 44,525 |
|
||
Liabilities, convertible preferred stock, and stockholders’ equity (deficit) | ||||||||
Current liabilities: | ||||||||
Accounts payable | $ | 3,077 |
|
$ | 1,187 |
|
||
Accrued expenses and other current liabilities | 6,651 |
|
1,372 |
|
||||
Current portion of long-term debt | — |
|
366 |
|
||||
Current portion of equipment loan payable | — |
|
113 |
|
||||
Total current liabilities | 9,728 |
|
3,038 |
|
||||
Equipment loan payable, net of current portion | - |
|
||||||
Long-term debt, net of current portion | — |
|
134 |
|
||||
Deferred rent | 12 |
|
8 |
|
||||
Total liabilities | 9,740 |
|
3,180 |
|
||||
Commitments and contingencies (Note 8) | ||||||||
Stockholders’ equity (deficit): | ||||||||
Preferred stock, |
— |
|
— |
|
||||
Common stock, |
1 |
|
1 |
|
||||
Additional paid-in capital | 127,289 |
|
95,738 |
|
||||
Accumulated deficit | (79,105 |
) |
(54,394 |
) |
||||
Total stockholders’ equity (deficit) | 48,185 |
|
41,345 |
|
||||
Total liabilities, convertible preferred stock, and stockholders’ equity (deficit) | $ | 57,925 |
|
$ | 44,525 |
|
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Immunome Contact
Chief Financial Officer
investors@immunome.com
Investor Contact
Managing Director
laurence@gilmartinir.com
Media Contact
Account Supervisor
gschanker@lifescicomms.com
Source:
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