AN2 Therapeutics Reports Second Quarter 2024 Financial Results and Recent Business and Scientific Highlights
14 8월 2024 - 5:01AM
Business Wire
Cash, cash equivalents, and investments of
$104.5 million at June 30, 2024; cash runway anticipated to fund
operations through 2027
AN2 Therapeutics, Inc. (Nasdaq: ANTX), a biopharmaceutical
company focused on discovering and developing novel small molecule
therapeutics derived from its boron chemistry platform today
reported financial results for the quarter ended June 30, 2024.
“We reported results from the EBO-301 Phase 2/3 study in
patients with treatment-refractory MAC lung disease last week and
over the coming months will further analyze the data to determine
next steps in NTM lung disease,” said Eric Easom, Co-Founder,
Chairman, President and CEO. “Despite this setback, we remain well
positioned as a company - we have a boron chemistry platform with
two development programs that are expected to advance into clinical
trials in 2025. AN2-502998 is expected to enter Phase 1 with an aim
to cure chronic Chagas disease, a potentially life-threatening
illness that causes severe cardiac disease and where there are
limited to no treatment options. We also plan to initiate a Phase 2
trial with epetraborole for the treatment of melioidosis, a deadly
bacterial infection and global bioterrorism threat. Additionally,
we have a pipeline of internally developed boron-based compounds in
research targeting high unmet needs in infectious disease and
oncology and we have the financial runway to allow us to achieve
multiple inflection points over the next three years.”
Second Quarter & Recent Business Updates:
Termination of Epetraborole Pivotal Phase 2/3 Clinical Study
in TR-MAC Lung Disease AN2 recently announced topline results
from the Phase 2 part of the EBO-301 Phase 2/3 study evaluating
epetraborole on top of an optimized background regimen in
treatment-refractory MAC lung disease. The Phase 2 part of the
study met its primary objective of demonstrating the potential
validation of a novel patient-reported outcome (PRO) tool and a
higher PRO-based clinical response rate in the epetraborole + OBR
arm vs. placebo + OBR. However, sputum culture conversion at Month
6, a key secondary endpoint, was similar between treatment arms.
Based on the topline data, the Company has terminated the Phase 2
and Phase 3 parts of the EBO-301 trial. Oral epetraborole 500 mg
daily was generally well-tolerated and the study was not terminated
due to safety concerns. The Company plans to further analyze the
EBO-301 data to better understand the results and their impact on
the ongoing development of epetraborole for nontuberculous
mycobacteria (NTM) lung disease.
Published New Epetraborole Data in Antimicrobial Agents in
Chemotherapy In July, the company published a study in the
journal Antimicrobial Agents in Chemotherapy, which highlighted the
efficacy of epetraborole against M. abscessus in a mouse lung
infection model. The study suggests that epetraborole could become
an important therapy to address the high unmet need for effective
oral treatment options for M. abscessus lung disease.
Selected Second Quarter Financial Results
- Research and Development (R&D) Expenses: R&D
expenses for the second quarter of 2024 were $12.1 million compared
to $13.5 million for the same period during 2023 due to decreased
chemistry manufacturing and controls activity and decreased
expenses for completed Phase 1 clinical trials, partially offset by
increased Phase 2/3 clinical trial costs, increased consulting and
outside service costs and increased personnel-related
expenses.
- General and Administrative (G&A) Expenses: G&A
expenses for the second quarter of 2024 were $3.7 million compared
to $3.1 million for the same period during 2023 due to an increase
in personnel-related expenses and professional and outside
services.
- Other Income, Net: Other income, net for the second
quarter of 2024 was $1.4 million compared to $0.8 million for the
same period during 2023 due to increased interest income based on
higher interest rates and higher cash, cash equivalents and
investment balances.
- Net loss: Net loss for the second quarter of 2024 was
$14.4 million, compared to $15.8 million for the same period during
2023.
- Cash Position: The Company had cash, cash equivalents,
and investments of $104.5 million at June 30, 2024, which is
expected to fund operations through 2027.
About AN2 Therapeutics, Inc.
AN2 Therapeutics, Inc. is a biopharmaceutical company focused on
discovering and developing novel small molecule therapeutics
derived from its boron chemistry platform. AN2 has a pipeline of
boron-based compounds in development for Chagas disease, NTM, and
melioidosis, along with early-stage programs focused on targets in
infectious diseases and oncology. For more information, please
visit our website at www.an2therapeutics.com.
Forward-Looking Statements
This press release contains forward-looking statements within
the meaning of the Private Securities Litigation Reform Act of
1995. Forward-looking statements expressed or implied in this press
release include, but are not limited to, statements regarding: the
Company’s plans to shift its focus to its internal boron chemistry
platform and ongoing pipeline programs; cash runway; analysis and
expectations regarding data analysis from the Phase 2/3 trial in
treatment-refractory MAC lung disease; future development of
epetraborole for M. abscessus and other forms of NTM; initiation,
advancement and timing of the Company’s clinical trials;
achievement and timing of potential inflection points; the ability
to identify development candidates for infectious diseases or
oncology targets; development of AN2-502998 for Chagas disease;
development of epetraborole for melioidosis; potential of the
Company’s boron chemistry platform and epetraborole; and other
statements that are not historical fact. These statements are based
on AN2’s current estimates, expectations, plans, objectives, and
intentions, are not guarantees of future performance and inherently
involve significant risks and uncertainties. Actual results and the
timing of events could differ materially from those anticipated in
such forward-looking statements as a result of these risks and
uncertainties, which include, but are not limited to, risks and
uncertainties related to: potential disruptions related to AN2’s
restructuring plans and its ability to implement its plans for its
internal boron chemistry platform and ongoing pipeline programs;
timely enrollment of patients in AN2’s existing and future clinical
trials; AN2’s ability to procure sufficient supply of its product
candidates for its existing and future clinical trials; the
potential for results from clinical trials to differ from
preclinical, early clinical, preliminary or expected results;
significant adverse events, toxicities or other undesirable side
effects associated with AN2’s product candidates; the significant
uncertainty associated with AN2’s product candidates ever receiving
any regulatory approvals; continued funding by the National
Institute of Allergy and Infectious Disease (NIAID) of the
Company’s development program for melioidosis; AN2’s ability to
obtain, maintain or protect intellectual property rights related to
its current and future product candidates; implementation of AN2’s
strategic plans for its business and product candidates; the
sufficiency of AN2’s capital resources and need for additional
capital to achieve its goals; global macroeconomic conditions and
global conflicts and other risks, including those described under
the heading “Risk Factors” in AN2’s Annual Reports on Form 10-K and
Quarterly Reports on Form 10-Q, and AN2’s other reports filed with
the U.S. Securities and Exchange Commission (SEC). These filings,
when made, are available on the investor relations section of AN2’s
website at www.an2therapeutics.com and on the SEC’s website at
www.sec.gov. Forward-looking statements contained in this press
release are made as of this date, and AN2 undertakes no duty to
update such information except as required under applicable
law.
AN2 THERAPEUTICS, INC.
CONDENSED STATEMENTS OF
OPERATIONS AND COMPREHENSIVE LOSS
(in thousands, except share
and per share data)
(unaudited)
Three Months Ended June
30,
Six Months Ended June
30,
2024
2023
2024
2023
Operating expenses:
Research and development
$
12,149
$
13,538
$
26,804
$
25,523
General and administrative
3,731
3,063
7,372
7,117
Total operating expenses
15,880
16,601
34,176
32,640
Loss from operations
(15,880
)
(16,601
)
(34,176
)
(32,640
)
Other income, net
1,445
797
3,124
1,513
Net loss attributable to common
stockholders
$
(14,435
)
$
(15,804
)
$
(31,052
)
$
(31,127
)
Net loss per share attributable to common
stockholders, basic and diluted
$
(0.48
)
$
(0.81
)
$
(1.04
)
$
(1.60
)
Weighted-average number of shares used in
computing net loss per share, basic and diluted
29,824,725
19,497,494
29,794,001
19,442,010
Other comprehensive loss:
Unrealized (loss) gain on investments
(80
)
56
(302
)
255
Comprehensive loss
$
(14,515
)
$
(15,748
)
$
(31,354
)
$
(30,872
)
AN2 THERAPEUTICS, INC.
CONDENSED BALANCE
SHEETS
(in thousands)
June 30, 2024
(unaudited)
December 31, 2023
Assets
Current assets:
Cash and cash equivalents
$
26,769
$
15,647
Short-term investments
77,771
91,648
Prepaid expenses and other current
assets
2,898
3,212
Long-term investments
—
27,194
Other assets, long-term
1,043
1,043
Total assets
$
108,481
$
138,744
Liabilities and stockholders’
equity
Current liabilities:
Accounts payable
$
1,885
$
2,676
Other current liabilities
8,242
11,367
Total liabilities
10,127
14,043
Stockholders’ equity
98,354
124,701
Total liabilities and stockholders’
equity
$
108,481
$
138,744
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version on businesswire.com: https://www.businesswire.com/news/home/20240813783660/en/
Lucy O. Day Chief Financial Officer
l.day@an2therapeutics.com
Anne Bowdidge Investor Relations
abowdidge@an2therapeutics.com
AN2 Therapeutics (NASDAQ:ANTX)
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