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Applied Molecular Transport Reports Fourth Quarter and Full Year 2022 Financial Results and Provides Corporate Update

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Applied Molecular Transport Inc. (Nasdaq: AMTI) released its corporate update and financial results for Q4 and full year 2022. The company is focusing on strategic partnerships to advance AMT-101, which has received FDA Orphan Drug Designation for chronic pouchitis. Notable highlights include presenting positive Phase 2 data at ECCO and anticipation of top-line results from the CASTRO trial in Rheumatoid Arthritis. Financially, R&D expenses rose by $18.4 million, while G&A expenses increased by $8.1 million. The net loss for Q4 2022 was $22.6 million, with an annual net loss of $126.3 million. Cash reserves stood at $61.1 million at year-end.

Positive
  • FDA granted Orphan Drug Designation for AMT-101.
  • Positive Phase 2 data presented at ECCO for AMT-101.
  • Upcoming top-line data readout for CASTRO trial anticipated in 2023.
Negative
  • R&D expenses increased by $18.4 million compared to 2021.
  • G&A expenses rose by $8.1 million compared to 2021.
  • Net loss for 2022 was $126.3 million, up from $100.3 million in 2021.
  • Cash and cash equivalents decreased from $159.8 million in 2021 to $61.1 million.

Exploring strategic partnership options to advance AMT-101 for chronic pouchitis, an orphan indication with no FDA-approved products

Evaluating next steps for the company's second clinical asset, AMT-126

SOUTH SAN FRANCISCO, Calif., March 09, 2023 (GLOBE NEWSWIRE) -- Applied Molecular Transport Inc. (Nasdaq: AMTI) (AMT), a clinical-stage biopharmaceutical company, today provided a corporate update and reported financial results for the fourth quarter and full year ended December 31, 2022.

“We were pleased to recently present additional positive AMT-101 translational data at ECCO for our Phase 2 FILLMORE monotherapy trial in patients with chronic pouchitis,” said Tahir Mahmood, Ph.D., chief executive officer and co-founder of AMT. “We remain focused on exploring a strategic partnership to advance AMT-101 for this important indication which has been granted Orphan Drug Designation by the FDA.”

Recent Business Highlights and Anticipated Milestones

  • Clinical asset AMT-101 (oral fusion of IL-10):
    • Presented additional Phase 2 FILLMORE trial translational data in patients with chronic pouchitis at the European Crohn’s and Colitis Organisation (ECCO) ’23 Congress
    • U.S. Food and Drug Administration granted Orphan Drug Designation for AMT-101 for the treatment of patients with pouchitis, an indication with significant unmet medical need and no current FDA-approved products
    • CASTRO combination trial with anti-TNFα in patients with Rheumatoid Arthritis who are partial or non-responders to anti-TNFα therapy; top-line data readout anticipated in 2023
  • Second clinical asset AMT-126 (oral fusion of IL-22):
    • Completed a Phase 1a clinical trial for AMT-126 in 2022
    • Presented initial Phase 1a healthy volunteer data at the Federation of Clinical Immunology Societies (FOCIS) Annual Meeting in June 2022
    • Evaluating next steps for the program

Financial Results for the Fourth Quarter and Full Year Ended December 31, 2022

Research and development (R&D) expenses. Research and development expenses increased by $18.4 million for the year ended December 31, 2022 compared to the year ended December 31, 2021. The overall increase was primarily driven by external costs related to the FILLMORE, LOMBARD and MARKET Phase 2 clinical trials and an increase in personnel-related expenses, including employee separation costs related to our strategic plan which was announced in May 2022 (Strategic Plan) and stock-based compensation expense.

General and administrative (G&A) expenses. General and administrative expenses increased by $8.1 million for the year ended December 31, 2022 compared to the year ended December 31, 2021. The increase was primarily due to higher personnel-related expenses, mainly from stock-based compensation expense and employee separation costs related to our Strategic Plan.

Net loss. Net loss for the fourth quarter of 2022 was $22.6 million, compared to a net loss of $30.2 million for the same period in 2021. Net loss for the year ended December 31, 2022 was $126.3 million, compared to $100.3 million for the year ended December 31, 2021.

Cash and cash equivalents. As of December 31, 2022, cash and cash equivalents were $61.1 million compared to $159.8 million for the year ended December 31, 2021.

About AMT-101

AMT-101 is a novel GI-selective, oral fusion of IL-10 and AMT’s proprietary carrier molecule, currently in development in Phase 2 clinical trials for chronic pouchitis and RA. AMT-101 is designed to cross the intestinal epithelial (IE) barrier with limited entry into the bloodstream, thereby focusing IL-10 at the primary site of inflammation in inflammatory bowel disease (IBD), along the intestinal tissue lamina propria, potentially avoiding the side effects observed with systemic administration.

About Applied Molecular Transport Inc.

AMT is a clinical-stage biopharmaceutical company developing novel oral biologic product candidates, by leveraging its technology platform to design and advance a multi-product pipeline. AMT is developing its oral biologic product candidates in patient-friendly oral dosage forms that are designed to either target local intestinal tissue or enter systemic circulation to precisely address the relevant pathophysiology of disease. AMT’s proprietary technology platform allows it to exploit existing natural cellular trafficking pathways to facilitate the active transport of diverse therapeutic modalities across the IE barrier. Active transport is an efficient mechanism that uses the cell’s own machinery to transport materials across the IE barrier.

AMT’s headquarters, internal GMP manufacturing and lab facilities are located in South San Francisco, CA. For additional information on AMT, please visit www.appliedmt.com.

Forward-Looking Statements

This press release contains forward-looking statements as that term is defined in Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. Such forward-looking statements involve substantial risks and uncertainties. All statements other than statements of historical facts contained in this press release are forward-looking statements including statements relating to AMT’s plans, expectations, forecasts and future events. Such forward-looking statements include, but are not limited to, statements regarding the potential of, and expectations regarding, AMT’s technology platform, product candidates, programs, including AMT-101 and AMT-126, and strategy; statements regarding AMT’s expectations relating to its milestones, clinical trials and clinical development, including timing of data readouts from its AMT-101 clinical trials; statements regarding the sufficiency of the Company’s cash resources; and statements by AMT’s chief executive officer and co-founder. In some cases, you can identify forward-looking statements by terminology such as “believe,” “estimate,” “intend,” “may,” “plan,” “potentially,” “will,” “expect,” “enable,” “likely” or the negative of these terms or other similar expressions. We have based these forward-looking statements largely on our current expectations and projections about future events and trends that we believe may affect our financial condition, results of operations, business strategy and financial needs. Actual events, trends or results could differ materially from the plans, intentions and expectations disclosed in these forward-looking statements based on various factors. Information regarding the foregoing and additional risks may be found in the section entitled “Risk Factors” in AMT’s Annual and Quarterly Reports on Form 10-K and 10-Q filed with the Securities and Exchange Commission (the “SEC”), and AMT’s future reports to be filed with the SEC. These forward-looking statements are made as of the date of this press release, and AMT assumes no obligation to update the forward-looking statements, or to update the reasons why actual results could differ from those projected in the forward-looking statements, except as required by law.


Applied Molecular Transport Inc.
Condensed Balance Sheets
(unaudited)
(in thousands)

 December 31,
  2022   2021 
Assets   
Current assets:   
Cash and cash equivalents$61,145  $159,821 
Prepaid expenses 2,688   6,685 
Other current assets 186   594 
Total current assets 64,019   167,100 
Property and equipment, net 8,183   6,998 
Operating lease right-of-use assets 33,222   38,142 
Finance lease right-of-use assets 584   652 
Restricted cash 916   1,025 
Other assets 522   121 
Total assets$107,446  $214,038 
Liabilities and stockholders’ equity   
Current liabilities:   
Accounts payable$1,583  $2,211 
Accrued expenses 8,660   8,226 
Lease liabilities, operating lease - current 4,639   3,584 
Lease liabilities, finance lease - current 205   237 
Total current liabilities 15,087   14,258 
Lease liabilities, operating lease 31,228   35,785 
Lease liabilities, finance lease 49   167 
Other liabilities 244   241 
Total liabilities 46,608   50,451 
Stockholders’ equity:   
Common stock 4   4 
Additional paid-in capital 426,804   403,228 
Accumulated deficit (365,970)  (239,645)
Total stockholders’ equity 60,838   163,587 
Total liabilities and stockholders’ equity$107,446  $214,038 


Applied Molecular Transport Inc.
Condensed Statements of Operations and Comprehensive Loss
(unaudited)
(in thousands, except share and per share amounts)

 Three Months Ended
December 31,
 Twelve Months
Ended December 31,
  2022   2021   2022   2021 
Operating expenses:       
Research and development$14,440  $21,683  $89,826  $71,448 
General and administrative 8,655   9,008   37,393   29,341 
Total operating expenses 23,095   30,691   127,219   100,789 
Loss from operations (23,095)  (30,691)  (127,219)  (100,789)
Interest income, net 505   522   898   626 
Other income (expense), net (9)  (34)  (4)  (124)
Net loss$(22,599) $(30,203) $(126,325) $(100,287)
Net loss per share, basic and diluted$(0.58) $(0.78) $(3.25) $(2.67)
Weighted-average shares of common stock outstanding, basic and diluted 39,038,116   38,536,106   38,837,001   37,591,505 
Comprehensive loss:       
Net loss$(22,599) $(30,203) $(126,325) $(100,287)
Other comprehensive loss:       
Unrealized loss on investments    (1)     (27)
Total comprehensive loss$(22,599) $(30,204) $(126,325) $(100,314)

-----------------------------------
Refer to the Company’s applicable SEC filings for previously reported periods.


Investor Relations Contact:
Alexandra Santos
Wheelhouse Life Science Advisors
asantos@wheelhouselsa.com

Media Contact:
Aljanae Reynolds
Wheelhouse Life Science Advisors
areynolds@wheelhouselsa.com


FAQ

What were the financial results for AMTI in Q4 2022?

AMTI reported a net loss of $22.6 million in Q4 2022.

How much did AMTI's net loss increase in 2022?

AMTI's net loss increased to $126.3 million in 2022, compared to $100.3 million in 2021.

What is the significance of AMT-101's Orphan Drug Designation?

The Orphan Drug Designation for AMT-101 allows for expedited development and market exclusivity for the treatment of chronic pouchitis.

When can we expect results from the CASTRO trial?

Top-line data from the CASTRO combination trial is anticipated in 2023.

Applied Molecular Transport Inc.

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