Last10K.com

Acumen Pharmaceuticals, Inc. (ABOS) SEC Filing 8-K Material Event for the period ending Monday, May 16, 2022

Acumen Pharmaceuticals, Inc.

CIK: 1576885 Ticker: ABOS

Exhibit 99.1

 

LOGO

Acumen Pharmaceuticals Reports Financial Results for

First Quarter 2022 and Business Highlights

 

   

Topline results expected in the first half of 2023 from INTERCEPT-AD, a multi-center, randomized, double-blind, placebo-controlled, single- and multiple-ascending dose Phase 1 clinical trial of ACU193 in patients with early Alzheimer’s disease

 

   

Frontiers in Neuroscience recently published a summary of preclinical evidence supporting the development of ACU193, a monoclonal antibody designed to selectively target toxic soluble amyloid-beta oligomers (AßOs), for the potential treatment of early Alzheimer’s disease

 

   

$216.7 million in cash, cash equivalents and marketable securities as of March 31, 2022, which is expected to provide cash runway through 2025

 

   

Company to host conference call and webcast today at 4:30 pm ET

Charlottesville, Va. and Carmel, In., May

 16, 2022Acumen Pharmaceuticals, Inc. (NASDAQ: ABOS), a clinical-stage biopharmaceutical company focused on the development of novel targeted therapeutics for Alzheimer’s disease (AD), today reported financial results for the quarter ended March 31, 2022 and provided a business update.

“During the first quarter, we made significant progress in advancing INTERCEPT-AD, our Phase 1 clinical trial investigating the safety, tolerability, pharmacokinetics and target engagement of ACU193 in patients with early AD. We expect to report topline results in the first half of 2023,” said Daniel O’Connell, President and Chief Executive Officer of Acumen. “Further, we expect our existing cash, cash equivalents and marketable securities will be sufficient to fund our operating expenses and capital expenditure requirements through 2025 based on our current plans.”

The Acumen team is pleased with the recent publication of the Frontiers in Neuroscience article in which preclinical evidence characterizing ACU193’s selectivity and differentiated profile is reviewed with the rationale for targeting soluble amyloid-beta oligomers in early AD. “The Frontiers article is timely, as we and others in the field look at upcoming clinical and regulatory events and as we continue to position ACU193 as potentially having a best-in-class treatment profile based on its potential safety, including anticipated limited to no ARIA-E, and clinical benefits on cognitive measures,” said Eric Siemers, Acumen’s Chief Medical Officer. “Each other monoclonal antibody which is approved or is in development has a different profile targeting various forms of Aß or amyloid. We believe the differences in these profiles are likely to lead to meaningful differences in the benefit-to-risk ratios of other products and product candidates and ACU193. The potential clinical significance of ACU193’s ability to selectively target toxic soluble AßOs is something we are excited to address in the clinic.”


LOGO

 

Recent Business Highlights and Anticipated Milestones

ACU193 Clinical Development

 

   

INTERCEPT-AD enrollment remains ongoing. Patient screening and enrollment is ongoing for INTERCEPT-AD. Acumen anticipates topline data from this trial in the first half of 2023, subject to the rate of site activation and patient recruitment.

 

   

Frontiers in Neuroscience recently published a comprehensive summary of preclinical evidence supporting ACU193 for the potential treatment of early Alzheimer’s disease. The article is titled “ACU193: An immunotherapeutic poised to test the amyloid ß oligomer hypothesis of Alzheimer’s disease” and can be accessed here.

 

   

Phase 2/3 clinical trial preparation activities progressing. Acumen plans to be ready to initiate a Phase 2/3 trial if INTERCEPT-AD results are positive. Chronic toxicology and chemistry manufacturing and controls (CMC) activities are ongoing to support readiness.

First Quarter 2022 Financial Results

 

   

Cash Balance. As of March 31, 2022, cash, cash equivalents and marketable securities totaled $216.7 million, compared to cash, cash equivalents and marketable securities of $225.9 million as of December 31, 2021. The decrease in cash is related to funding ongoing operations.

 

   

Research and Development (R&D) Expenses. R&D expenses were $6.0 million for the three-month period ended March 31, 2022, compared to $2.6 million for the three-month period ended March 31, 2021. The increase in research and development expenses was primarily due to increased costs related to our ongoing clinical trial which was initiated in 2021.

 

   

General and Administrative (G&A) Expenses. G&A expenses were $3.2 million for the three-month period ended March 31, 2022, compared to $1.2 million for the three-month period ended March 31, 2021. The increase in general and administrative expenses was primarily due to increased costs related to being a public company.

 

   

Loss from Operations. Losses from operations were $9.2 million for the three-month period ended March 31, 2022, compared to $3.8 million for the three-month period ended March 31, 2021.

 

   

Net Loss. Net loss was $9.1 million for the three-month period ended March 31, 2022, compared to $27.0 million for the three-month period ended March 31, 2021. Net losses in the 2021 period includes a $23.2 million non-cash expense that represents the changes in fair value of Acumen’s Series B tranche liability and Series A-1 warrant liability. The remaining increase relates to increased operating expenses.

Conference Call Details

Acumen will host a conference call and live audio webcast today, May 16, at 4:30 pm ET. The live webcast may be accessed from the Investors section of the Company’s website at www.acumenpharm.com. Please connect to the website prior to the start of the conference call to ensure adequate time for any software downloads that may be necessary. Investors may participate in the conference call by dialing +1 877 311-0573 in the U.S., or +1 470 495-9505 outside the U.S., and entering passcode 2586595.

 

2


LOGO

 

An archived version of the webcast will be available for at least 30 days in the Investors section of the Company’s website at www.acumenpharm.com.

About ACU193

ACU193 is a humanized monoclonal antibody (mAb) discovered and developed based on its selectivity for soluble AßOs, which Acumen believes are the most toxic and pathogenic form of Aß, relative to Aß monomers and amyloid plaques. Soluble AßOs have been observed to be potent neurotoxins that bind to neurons, inhibit synaptic function and induce neurodegeneration. By selectively targeting toxic soluble AßOs, ACU193 aims to directly address what a growing body of evidence indicates is a primary underlying cause of the neurodegenerative process in AD.

About INTERCEPT-AD

Approximately 62 individuals with early AD (mild cognitive impairment or mild dementia due to AD) are expected to be randomized into this double-blind, placebo-controlled, first-in-human study of ACU193. INTERCEPT-AD is designed to establish safety and proof of mechanism. It consists of single-ascending-dose (SAD) and multiple-ascending-dose (MAD) cohorts and is designed to evaluate the safety, tolerability, pharmacokinetics (PK), and target engagement of intravenous doses of ACU193. The study is enrolling at multiple investigative sites located in the United States. More information can be found on www.clinicaltrials.gov, NCT identifier NCT04931459.

About Acumen Pharmaceuticals, Inc.

Acumen Pharmaceuticals, headquartered in Charlottesville, VA, with clinical operations based in Carmel, IN., is a clinical stage biopharmaceutical company developing a novel disease-modifying approach to treat Alzheimer’s disease. Acumen’s scientific founders pioneered research on toxic soluble AßOs, which a growing body of evidence indicates are primary triggers of Alzheimer’s disease pathology. Acumen is currently focused on advancing its investigational product candidate, ACU193, a humanized monoclonal antibody that selectively targets toxic soluble AßOs in a Phase 1 clinical trial involving early Alzheimer’s disease patients. For more information, visit www.acumenpharm.com.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995. Any statement describing Acumen’s goals, expectations, financial or other projections, intentions or beliefs is a forward-looking statement and should be considered an at-risk statement. Words such as “believes,” “expects,” “anticipates,” “could,” “would,” “seeks,” “aims,” “plans,” “potential,” “will” and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Forward-looking statements include statements concerning Acumen’s business, Acumen’s ability to achieve its strategic and financial goals, including its projected use of cash, cash equivalents and marketable securities and the sufficiency of its cash resources, and the therapeutic potential of Acumen’s product candidate,

 

3


LOGO

 

ACU193, including its potential for improved safety and efficacy as compared to other monoclonal antibodies in development, as well as the expectations concerning the INTERCEPT-AD trial and Acumen’s planned Phase 2/3 clinical trial, including the anticipated number of trial sites, enrollment objectives and the expected timing of reporting data, and risks and uncertainties relating to the progression and duration of the COVID-19 pandemic and responsive measures thereto and related effects on Acumen. These statements are based upon the current beliefs and expectations of Acumen management, and are subject to certain factors, risks and uncertainties, particularly those inherent in the process of discovering, developing and commercializing safe and effective human therapeutics. Such risks may be amplified by the impacts of the COVID-19 pandemic. These and other risks concerning Acumen’s programs are described in additional detail in Acumen’s filings with the Securities and Exchange Commission (“SEC”), including in Acumen’s Annual Report on Form 10-K for the fiscal year ended December 31, 2021, and future filings and reports by Acumen, including Acumen’s Quarterly Report on Form 10-Q for the quarter ended March 31, 2022. Copies of these and other documents are available from Acumen. Additional information will be made available in other filings that Acumen makes from time to time with the SEC. These forward-looking statements speak only as of the date hereof, and Acumen expressly disclaims any obligation to update or revise any forward-looking statement, except as otherwise required by law, whether, as a result of new information, future events or otherwise.

Investor & Media Contact:

investors@acumenpharm.com

 

4


LOGO

 

Acumen Pharmaceuticals, Inc.

Condensed Balance Sheets

(in thousands, except share and per share data)

 

     March 31, 2022     December 31, 2021  
     (unaudited)        

ASSETS

    

Current assets

    

Cash and cash equivalents

   $ 108,764     $ 122,162  

Marketable securities, short-term

     80,326       72,075  

Prepaid expenses and other current assets

     3,008       4,424  
  

 

 

   

 

 

 

Total current assets

     192,098       198,661  

Marketable securities, long-term

     27,658       31,619  

Property and equipment, net

     51       36  

Right-of-use asset

     201       —    

Other assets

     79       14  
  

 

 

   

 

 

 

Total assets

   $ 220,087     $ 230,330  
  

 

 

   

 

 

 

LIABILITIES AND STOCKHOLDERS’ EQUITY

    

Current liabilities

    

Accounts payable

   $ 1,219     $ 1,088  

Accrued expenses and other current liabilities

     2,578       4,059  

Operating lease liability, current portion

     139       —    
  

 

 

   

 

 

 

Total current liabilities

     3,936       5,147  

Operating lease liability, net of current portion

     62       —    
  

 

 

   

 

 

 

Total liabilities

     3,998       5,147  

Commitments and contingencies

    

Stockholders’ equity

    

Preferred stock, $0.0001 par value; 10,000,000 shares authorized and no shares issued and outstanding as of March 31, 2022 and December 31, 2021

     —         —    

Common stock, $0.0001 par value; 300,000,000 shares authorized and 40,473,270 shares issued and outstanding as of March 31, 2022 and December 31, 2021

     4       4  

Additional paid-in capital

     353,599       352,981  

Accumulated deficit

     (136,700     (127,571

Accumulated other comprehensive loss

     (814     (231
  

 

 

   

 

 

 

Total stockholders’ equity

     216,089       225,183  
  

 

 

   

 

 

 

Total liabilities and stockholders’ equity

   $ 220,087     $ 230,330  
  

 

 

   

 

 

 

 

5


LOGO

 

Acumen Pharmaceuticals, Inc.

Condensed Statements of Operations and Comprehensive Loss

(in thousands, except share and per share data)

(unaudited)

 

     Three Months Ended March 31,  
     2022     2021  

Operating expenses

    

Research and development

   $ 5,985     $ 2,578  

General and administrative

     3,221       1,215  
  

 

 

   

 

 

 

Total operating expenses

     9,206       3,793  
  

 

 

   

 

 

 

Loss from operations

     (9,206     (3,793

Other income (expense)

    

Interest income, net

     76       4  

Change in fair value of preferred stock tranche rights liability and preferred stock warrant liability

     —         (23,217

Other income, net

     1       9  
  

 

 

   

 

 

 

Total other income (expense)

     77       (23,204
  

 

 

   

 

 

 

Net loss

     (9,129     (26,997
  

 

 

   

 

 

 

Other comprehensive loss

    

Unrealized loss on marketable securities

     (583     —    
  

 

 

   

 

 

 

Comprehensive loss

   $ (9,712   $ (26,997
  

 

 

   

 

 

 

Net loss per common share, basic and diluted

   $ (0.23   $ (64.41
  

 

 

   

 

 

 

Weighted-average shares outstanding, basic and diluted

     40,473,270       419,124  
  

 

 

   

 

 

 

 

6


LOGO

 

Acumen Pharmaceuticals, Inc.

Condensed Statements of Cash Flows

(in thousands)

(unaudited)

 

     Three Months Ended March 31,  
     2022     2021  

Cash flows from operating activities

  

Net loss

   $ (9,129   $ (26,997

Adjustments to reconcile net loss to net cash used in operating activities:

    

Depreciation

     4       —    

Change in fair value of preferred stock tranche rights liability and preferred stock warrant liability

     —         23,217  

Stock-based compensation expense

     618       126  

Amortization of premiums and accretion of discounts on marketable securities, net

     216       —    

Amortization of right-of-use asset

     33       —    

Changes in operating assets and liabilities:

    

Prepaid expenses and other current assets

     1,416       (44

Other assets

     (65     (13

Accounts payable

     121       387  

Operating lease liability

     (32     —    

Accrued expenses and other current liabilities

     (1,481     954  
  

 

 

   

 

 

 

Net cash used in operating activities

     (8,299     (2,370
  

 

 

   

 

 

 

Cash flows from investing activities

    

Purchases of marketable securities

     (9,090     —    

Proceeds from maturities and sales of marketable securities

     4,000       —    

Purchases of property and equipment

     (9     —    
  

 

 

   

 

 

 

Net cash used in investing activities

     (5,099     —    
  

 

 

   

 

 

 

Net change in cash and cash equivalents

     (13,398     (2,370

Cash and cash equivalents at the beginning of the period

     122,162       43,777  
  

 

 

   

 

 

 

Cash and cash equivalents at the end of the period

   $ 108,764     $ 41,407  
  

 

 

   

 

 

 

Supplemental disclosure of cash flow information

    

Cash paid for income taxes

   $ —       $ —    
  

 

 

   

 

 

 

Cash paid for interest

   $ —       $ —    
  

 

 

   

 

 

 

Supplemental disclosure of noncash investing and financing activities

    

Purchases of property and equipment in accounts payable

   $ 10     $ —    
  

 

 

   

 

 

 

Deferred offering costs in accrued expenses and other current liabilities

   $ —       $ 257  
  

 

 

   

 

 

 

 

7

View differences made from one to another to evaluate Acumen Pharmaceuticals, Inc.'s financial trajectory

Compare SEC Filings Year-over-Year (YoY) and Quarter-over-Quarter (QoQ)
Sample 10-K Year-over-Year (YoY) Comparison

Compare this 8-K Corporate News to its predecessor by reading our highlights to see what text and tables were  removed  ,   added    and   changed   by Acumen Pharmaceuticals, Inc..

Continue

Assess how Acumen Pharmaceuticals, Inc.'s management team is paid from their Annual Proxy

Definitive Proxy Statement (Form DEF 14A)
Screenshot example of actual Proxy Statement

Acumen Pharmaceuticals, Inc.'s Definitive Proxy Statement (Form DEF 14A) filed after their 2022 10-K Annual Report includes:

  • Voting Procedures
  • Board Members
  • Executive Team
  • Salaries, Bonuses, Perks
  • Peers / Competitors

Continue

SEC Filing Tools

Financial Statements, Disclosures and Schedules

Inside this 8-K Corporate News

Material Contracts, Statements, Certifications & more

Acumen Pharmaceuticals, Inc. provided additional information to their SEC Filing as exhibits

Ticker: ABOS
CIK: 1576885
Form Type: 8-K Corporate News
Accession Number: 0001193125-22-151761
Submitted to the SEC: Mon May 16 2022 4:18:17 PM EST
Accepted by the SEC: Mon May 16 2022
Period: Monday, May 16, 2022
Industry: Biological Products No Disgnostic Substances
Events:
  1. Earnings Release
  2. Financial Exhibit

External Resources:
Stock Quote
Social Media

Bookmark the Permalink:
https://last10k.com/sec-filings/abos/0001193125-22-151761.htm