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Azitra, Inc. Announces Full Year 2023 Financial Results and Provides Business Updates BRANFORD, Conn.-(BUSINESS WIRE)-Azitra, Inc. (NYSE American: AZTR), a clinical-stage biopharmaceutical company focused on developing i

Key Takeaway: Azitra, Inc. announced its full-year financial results for 2023, highlighting key business developments, including financial achievements and clinical progress. The company successfully completed an IPO and a follow-on offering, raising a total of $12.5 million. They obtained IND clearance for ATR-12, which is set to enter a Phase 1b clinical trial for Netherton syndrome, and advanced their program ATR-04 into IND-enabling studies. The company reported a net loss of $11.3 million for 2023, reflecting ongoing financial challenges amid a strong focus on innovation in precision dermatology.

Market Sentiment Analysis

POSITIVE FACTORS

  • Azitra successfully raised $7.5 million in an IPO and $5.0 million in a follow-on public offering.
  • The company obtained IND clearance for the Phase 1b clinical trial of ATR-12 targeting Netherton syndrome.
  • Azitra strengthened its IP portfolio with a new U.S. patent for treatments using recombinant microorganisms.
  • Progress in clinical trials and partnerships, including collaboration discussions with Bayer, signify ongoing growth.

CONCERNS & RISKS

  • Azitra reported a net loss of $11.3 million for 2023, indicating financial challenges.
  • Research and development expenses decreased, raising questions about the company's future innovation capacity.
  • Investment in clinical programs requires ongoing capital, and potential delays in regulatory approvals could hinder progress.
  • Dependence on third-party organizations for clinical testing poses risks to timely product development.

Full Press Release Details

Inc. Announces Full Year 2023 Financial Results and Provides Business Updates
Conn.-(BUSINESS WIRE)-Azitra, Inc. (NYSE American: AZTR), a clinical-stage biopharmaceutical company focused on developing
innovative therapies for precision dermatology, today reported financial results for the full year ended December 31, 2023, and provided
2023 and Recent Business Highlights
Completed an initial public offering, raising $7.5 million in gross proceeds.
Obtained IND clearance of ATR-12 for a Phase 1b clinical trial in Netherton syndrome.
Completed and filed post-IND, FDA commitments for characterization of drug substance and drug product for ATR-12.
Selected and hired clinical research organization for ATR-12 clinical trial and selected initial clinical sites for activation.
Advanced ATR-04 into IND-enabling studies.
Advanced Bayer Joint Development Agreement and discussions with Bayer for a license agreement.
Strengthened IP portfolio with U.S. patent issuance from the USPTO for treating skin diseases with recombinant microorganisms, including ichthyosis vulgaris, a condition affecting about 1.3 million Americans.
Named Travis Whitfill COO and added Barbara Ryan and John Schroer to board of directors.
Successfully completed a follow-on public offering in February 2024, raising $5.0 million in gross proceeds.
2023 and now into 2024, Azitra's unwavering commitment to combatting multiple serious skin conditions and diseases has propelled
the company towards fundamental near-term catalysts," said Francisco Salva, CEO of Azitra. "For our leading program, ATR-12
targeting Netherton's syndrome, we've transitioned into the operational phase for our Phase 1b clinical trial. With a CRO
onboard and discussions finalized with lead sites to activate the program and recruit ~12 patients, we're poised to execute on
a series of potentially high-impact catalysts. Moving forward, we're focused on executing on key value-driving milestones, including
getting the first patient enrolled, and a release of initial clinical data."
for our ATR-04 program targeting EGFRi-associated rash, we intend to submit an IND for a Phase 1b clinical trial in cancer patients undergoing
EGFRi targeted therapy in mid-2024. Subject to FDA clearance of our IND, we plan to initiate a Phase 1b clinical trial by year end.
regarding our Joint Development Agreement with Bayer, we are pleased with the recent progress of our collaboration and Bayer's
re-affirmed commitment to an execution of a license agreement."
and Upcoming Milestones
Clinical Status: Phase 1b
Upcoming milestones:
First patient dosed in 12-patient clinical trial
Publication of preclinical data at major medical meetings in Q2 2024
Initial clinical safety data in late 2024
Clinical Status: Pre-IND
Upcoming milestones:
Publication of preclinical data at major medical meetings in Q2 2024
IND submission in mid-2024
First patient dosed in first-in-human clinical trial in late 2024 or early 2025
Status: Azitra is responsible for early research, and Bayer is responsible for clinical development and commercialization
Upcoming milestones:
Results for the Year Ended December 31, 2023
Service Revenue - Related Party : The Company generated $0.7 million of service revenue during the year ended December 31, 2023, compared to $0.3 million for the comparable period in 2022.
Research and Development (R&D) expenses : R&D expenses for the year ended December 31, 2023, were $3.8 million compared to $6.1 million for the comparable period in 2022.
General and Administrative (G&A) expenses : G&A expenses for the year ended December 31, 2023, were $4.5 million compared to $3.6 million for the comparable period in 2022.
Net Loss was $11.3 million for the year ended December 31, 2023, compared to $10.7 million for the comparable period in 2022.
Cash and cash equivalents : As of December 31, 2023, the Company had cash and cash equivalents of $1.8 million, which does not include net proceeds of approximately $4.4 million from a February 15, 2024, follow-on offering.
Inc. is an early-stage clinical biopharmaceutical company focused on developing innovative therapies for precision dermatology using
engineered proteins and topical live biotherapeutic products. The Company has built a proprietary platform that includes a microbial
library comprised of approximately 1,500 unique bacterial strains that can be screened for unique therapeutic characteristics. The platform
is augmented by artificial intelligence and machine learning technology that analyzes, predicts, and helps screen the Company's
library of strains for drug like molecules. The Company's initial focus is on the development of genetically engineered strains
of Staphylococcus epidermidis, or S. epidermidis, which the Company considers to be an optimal therapeutic candidate species for
engineering of dermatologic therapies. For more information, please visit https://azitrainc.com/.
press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended.
These statements may be identified by words such as "aims," "anticipates," "believes," "could,"
"estimates," "expects," "forecasts," "goal," "intends," "may,"
"plans," "possible," "potential," "seeks," "will," and variations of these
words or similar expressions that are intended to identify forward-looking statements. Any such statements in this press release that
are not statements of historical fact may be deemed to be forward-looking statements. These forward-looking statements include, without
limitation, statements regarding the expected timing of the presentation of data from the Phase 1b study of ATR-12, the filing of an
IND application, and the presentation of data from our Phase 1b for ATR-04, the IND filing for ATR-01, the timing of having a signed
license agreement with Bayer, and statements about our clinical and pre-clinical programs, and corporate and clinical/pre-clinical strategies.
forward-looking statements in this press release are based on current expectations, estimates and projections only as of the date of
this release and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely
from those set forth in or implied by such forward-looking statements. These risks and uncertainties include, but are not limited to
that we may fail to successfully complete our Phase 1b trial for ATR-12 and pre-clinical studies of other product candidates and obtain
required approval before commercialization; our product candidates may not be effective; there may be delays in regulatory approval or
changes in regulatory framework that are out of our control; our estimation of addressable markets of our product candidates may be inaccurate;
we may fail to timely raise additional required funding; more efficient competitors or more effective competing treatment may emerge;
we may be involved in disputes surrounding the use of our intellectual property crucial to our success; we may not be able to attract
and retain key employees and qualified personnel; earlier study results may not be predictive of later stage study outcomes; and we are
dependent on third-parties for some or all aspects of our product manufacturing, research and preclinical and clinical testing. Additional
risks concerning Azitra's programs and operations are described in its registration statement on Form S-1, which is on file with
the SEC, and in its most recent annual report on Form 10-K to be filed with the SEC. Azitra explicitly disclaims any obligation to update
any forward-looking statements except to the extent required by law.
Chief Financial Officer
Consolidated Statement of Operations
2023 2022
Service revenue - related party $ 686,000 $ 284,000
Total revenue 686,000 284,000
Operating expenses:
General and administrative 4,493,332 3,639,666
Research and development 3,809,063 6,097,938
Total operating expenses 8,302,395 9,737,604
Loss from operations (7,616,395 ) (9,453,604 )
Non- operating income (expense):
Interest income 1,577 4,818
Interest expense (167,726 ) (251,891 )
Employee retention credit - 229,813
Other income - 65,849
Forgiveness of accounts payable 56,285 -
Change in fair value of convertible note (3,630,100 ) (1,250,000 )
Other income (expense) 89,886 (25,351 )
Total non-operating expenses (3,650,078 ) (1,226,762 )
Loss before income taxes (11,266,473 ) (10,680,366 )
Income tax benefit (expense) (17,308 )
Net loss $ (11,283,781 ) (10,680,366 )
Dividends on preferred stock (1,355,347 ) (2,768,984 )
Net loss attributable to common shareholders $ (12,639,128 ) (13,449,350 )
Net loss per Share, basic and diluted (1.83 ) (12.74 )
Weighted average common stock outstanding, basic and diluted $ 6,924,453 $ 1,055,399
Consolidated Balance Sheets
December 31, December 31,
2023 2022
Assets
Current Assets:
Cash and cash equivalents $ 1,795,989 $ 3,492,656
Other receivables 223,474 266,208
Prepaid expenses and other current assets 516,116 377,019
Total current assets $ 2,535,579 $ 4,135,883
Property and equipment, net 710,075 846,958
Other assets 1,869,832 2,184,602
Total assets $ 5,115,486 $ 7,167,443
Liabilities, preferred stock, and stockholders' equity
Current liabilities:
Accounts payable $ 897,272 $ 784,687
Current financing lease liability 14,600 -
Current operating lease liability 307,655 287,384
Accrued expenses 383,668 993,961
Contract liabilities - 156,000
Total current liabilities 1,603,195 2,222,032
Long-term financing lease liability 26,169 -
Long-term operating lease liability 537,523 840,896
Warrant liability 35,453 70,283
Convertible notes payable, net 0 6,600,000
Total liabilities 2,202,340 9,733,211
Stockholders' equity (deficit)
Preferred stock 0 33,694,542
Common stock 1,210 104
Additional paid-in capital 51,510,269 1,054,138
Accumulated deficit (48,598,333 ) (37,314,552 )
Total stockholders' equity (deficit) 2,913,146 (36,260,310 )
Total liabilities, preferred stock and stockholders' equity (deficit) $ 5,115,486 $ 7,167,443

Frequently Asked Questions

What finances did Azitra report for 2023?

Azitra reported a net loss of $11.3 million for 2023, an increase from $10.7 million in 2022.

What is ATR-12 targeting?

ATR-12 is being developed for the treatment of Netherton syndrome in a Phase 1b clinical trial.

How much did Azitra raise in its IPO?

Azitra raised $7.5 million in gross proceeds from its initial public offering.

What is the role of Bayer in Azitra's development?

Bayer is responsible for clinical development and commercialization under their joint development agreement.

What upcoming milestone is planned for ATR-04?

Azitra plans to submit an IND for a Phase 1b trial of ATR-04 by mid-2024.

Last updated: Mar 15, 2024