Annexon Biosciences Reports Second Quarter 2020 Financial Results and Recent Highlights - Annexon Biosciences



clinical pipeline
for diseases of the body, brain & eye

Annexon Biosciences Reports Second Quarter 2020 Financial Results and Recent Highlights

September 08, 2020

– Completed $263M IPO in July, and private financing in late June –

– Company plans to initiate four new clinical trials by year-end, including in three expanded indications for ANX005 and first-in-human trial of ANX009 –

– Phase 2 trials of ANX005 in GBS and ANX007 in GA remain on track for 2021 –

SOUTH SAN FRANCISCO, Calif., Sept. 08, 2020 (GLOBE NEWSWIRE) -- Annexon, Inc. (“Annexon”) (Nasdaq: ANNX), a clinical-stage biopharmaceutical company developing a pipeline of novel therapies for patients with classical complement-mediated disorders of the body, brain and eye, today announced second quarter 2020 financial results and recent highlights.

“This is an exciting time in Annexon’s history as we advance our pioneering platform to treat a wide array of classical complement-mediated diseases,” said Douglas Love, Esq., president and chief executive officer of Annexon. “We continue to make notable progress advancing our deep pipeline, and remain intensely focused on the execution of our near-term strategic and development plans. In that regard, we remain on track to initiate several clinical trials in diverse diseases over the balance of 2020 and early 2021.”

Recent Highlights

Anticipated Upcoming Milestones

Second Quarter 2020 Financial Results:

About Annexon, Inc.

Annexon is a clinical-stage biopharmaceutical company developing a pipeline of novel therapies for patients with classical complement-mediated disorders of the body, brain and eye. The company’s pipeline is based on its platform technology addressing well-researched classical complement-mediated autoimmune and neurodegenerative disease processes, both of which are triggered by aberrant activation of C1q, the initiating molecule of the classical complement pathway. The company’s first product candidate, ANX005, is a full-length monoclonal antibody formulated for intravenous administration in autoimmune and neurodegenerative disorders. The company’s second product candidate, ANX007, is a monoclonal antibody Fab formulated for intravitreal administration for the treatment of neurodegenerative ophthalmic disorders. Annexon is advancing its current programs while evaluating additional orphan and large market indications. Annexon is deploying a disciplined, biomarker-driven development strategy designed to establish that its product candidates are engaging the target at a well-tolerated therapeutic dose in the intended patient tissue. For more information, visit

Forward Looking Statements

This press release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended (Securities Act), and Section 21E of the Securities Exchange Act of 1934, as amended. In some cases, you can identify forward-looking statements by terminology such as “aim,” “anticipate,” “assume,” “believe,” “contemplate,” “continue,” “could,” “design,” “due,” “estimate,” “expect,” “goal,” “intend,” “may,” “objective,” “plan,” “positioned,” “potential,” “predict,” “seek,” “should,” “target,” “will,” “would” and other similar expressions that are predictions of or indicate future events and future trends, or the negative of these terms or other comparable terminology. All statements other than statements of historical facts contained in this press release are forward-looking statements. These forward-looking statements include, but are not limited to, statements about:  advancement of the company’s clinical and preclinical programs; timing and commencement of future nonclinical studies and clinical trials and research and development programs; and the implementation of the company’s business model and strategic plans for its business and product candidates, including additional indications which the company may pursue. Forward-looking statements are not guarantees of future performance and are subject to risks and uncertainties that could cause actual results and events to differ materially from those anticipated, including, but not limited to, risks and uncertainties related to:  the company’s history of net operating losses; the company’s ability to obtain necessary capital to fund its clinical programs; the early stages of clinical development of the company’s product candidates; the effects of COVID-19 or other public health crises on the company’s clinical programs and business operations; the company’s ability to obtain regulatory approval of and successfully commercialize its product candidates; any undesirable side effects or other properties of the company’s product candidates; the company’s reliance on third-party suppliers and manufacturers; the outcomes of any future collaboration agreements; and the company’s ability to adequately maintain intellectual property rights for its product candidates. These and other risks are described in greater detail under the section titled “Risk Factors” contained in the company’s prospectus filed with the Securities and Exchange Commission (SEC) on July 24, 2020 pursuant to Rule 424(b) under the Securities Act and the company’s other filings with the SEC. Any forward-looking statements that the company makes in this press release are made pursuant to the Private Securities Litigation Reform Act of 1995, as amended, and speak only as of the date of this press release. Except as required by law, the company undertakes no obligation to publicly update any forward-looking statements, whether as a result of new information, future events or otherwise.


Condensed Consolidated Statements of Operations
(in thousands, except share and per share amounts)

  Three Months Ended
June 30,
  Six Months Ended
June 30,  
    2020       2019       2020         2019    
Operating expenses:        
Research and development (1) $                9,287     $               5,987     $          19,504     $          10,640  
General and administrative (1)   2,950       2,230       5,189       3,679  
Total operating expenses   12,237       8,217       24,693       14,319  
Loss from operations   (12,237 )     (8,217 )     (24,693 )     (14,319 )
Loss on remeasurement of redeemable convertible preferred
stock liability
        (1,560 )           (4,330 )
Other income, net   1       376       116       597  
Net loss before taxes   (12,236 )     (9,401 )     (24,577 )     (18,052 )
Provision for income taxes   4             4       1  
Net loss   (12,240 )     (9,401 )     (24,581 )     (18,053 )
Accretion on redeemable convertible preferred stock   281       272       560       534  
Net loss attributable to common stockholders $           (12,521 )   $            (9,673 )   $       (25,141 )   $       (18,587 )
Net loss per share attributable to common stockholders, basic and
$              (28.87 )   $             (22.30 )   $          (57.96 )   $          (42.90 )
Weighted-average shares used in computing net loss per share
attributable to common stockholders, basic and diluted
  433,749       433,749       433,749       433,232  


(1)    Includes the following stock-based compensation expense:              
Research and development 335   135   660   232
General and administrative 428   302   766   671


Condensed Consolidated Balance Sheets
(in thousands)

  June 30,
    December 31,
Current assets:    
Cash and cash equivalents $     124,761     $         43,931  
Prepaid expenses and other current assets   907       1,475  
Total current assets   125,668       45,406  
Property and equipment, net   2,048       2,138  
Other long-term assets   3,371       2,354  
Total assets $     131,087     $         49,898  
Liabilities, Redeemable Convertible Preferred Stock and Stockholders’ Deficit    
Current liabilities:    
Accounts payable $          3,064     $           2,371  
Accrued liabilities   9,218       2,194  
Deferred rent, current   378       366  
Total current liabilities   12,660       4,931  
Deferred rent   1,247       1,437  
Total liabilities   13,907       6,368  
Redeemable convertible preferred stock   235,054       143,984  
Stockholders’ Deficit:    
 Common stock   4       4  
Additional paid-in capital   9,365       2,202  
Accumulated other comprehensive loss   (82 )     (80 )
Accumulated deficit   (127,161 )     (102,580 )
Total stockholders’ deficit   (117,874 )     (100,454 )
Total liabilities, redeemable convertible preferred stock and stockholders’ deficit $     131,087     $         49,898  

Investor Contact:
Sylvia Wheeler

Alexandra Santos

Media Contact:
Sara Michelmore 


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