Azitra, Inc. Announces Q2 2026 Results and Provides Business Updates
Rhea-AI Summary
Azitra (NYSE American: AZTR) reported Q2 2026 results and pipeline updates. R&D expenses were $1.4 million, flat year over year, while G&A rose to $2.1 million from $1.5 million. Net loss increased to $3.3 million versus $2.9 million in Q2 2025. Cash and cash equivalents were $6.7 million at June 30, 2026, up from $2.1 million at December 31, 2025.
Azitra reported first preclinical data for ATR-COSF, showing repeat-dose delivery, skin-layer targeting and anti-wrinkle activity in ex vivo human skin, with a cosmetic proof-of-concept study planned to start in Q3 2026. The company continued enrolling the first cohort in its Phase 1/2 trial of ATR-04 for EGFR inhibitor-associated rash, with topline data expected in Q4 2026, advanced recombinant protein programs (TEV Protease and T7 RNA Polymerase), and decided to pause further enrollment in the ATR-12 Phase 1b Netherton syndrome trial to prioritize capital.
Positive
- Cash position strengthened to $6.7 million at June 30, 2026, from $2.1 million at December 31, 2025
- ATR-COSF preclinical data showed targeted repeat-dose delivery and anti-wrinkle activity in ex vivo human skin
- ATR-04 Phase 1/2 trial first cohort enrolling with topline data expected in Q4 2026
- Recombinant protein portfolio expanded to TEV Protease and T7 RNA Polymerase for research and manufacturing markets
- Total assets increased to $8.9 million and stockholders’ equity to $7.3 million at June 30, 2026, from $5.0 million and $3.8 million at year-end 2025
Negative
- Net loss rose to $3.35 million in Q2 2026 from $2.89 million in Q2 2025
- G&A expenses increased to $2.07 million from $1.47 million year over year in Q2
- Accumulated deficit widened to $75.8 million at June 30, 2026, from $68.5 million at December 31, 2025
- ATR-12 Phase 1b enrollment in Netherton syndrome strategically paused, delaying further clinical progress in that indication
- Weighted average shares outstanding increased to 19.3 million in Q2 2026 from 2.44 million in Q2 2025, spreading results over a larger share base
Key Figures
Previous Earnings Reports
| Date | Event | Sentiment | 24h Move | Catalyst |
|---|---|---|---|---|
| May 13 | Q1 earnings report | Positive | -1.5% | Clinical progress, financing plans, and new cosmetic initiative were followed by a -1.5% reaction. |
| Feb 27 | FY earnings report | Positive | -6.1% | Clinical advances and Fast Track designation accompanied financial losses and a -6.06% reaction. |
| Nov 12 | Q3 earnings report | Negative | -14.6% | Higher net loss and equity financing activity accompanied pipeline progress and a -14.64% reaction. |
| Aug 11 | Q2 earnings report | Positive | -7.6% | Trial enrollment progress and funding access were followed by a -7.61% reaction. |
| May 13 | Q1 earnings report | Positive | -0.7% | Funding arrangements and ATR-04 planning were followed by a -0.68% reaction. |
24h Move is the share-price change in the day after each event; other market factors may also have contributed.
Tag-matched earnings events produced negative 24-hour reactions in all five prior observations, with an average move of -6.1%.
Key Terms
ex vivo medical
phase 1/2 clinical trial medical
recombinant protein technical
fast track designation regulatory
AI-generated analysis. How Rhea-AI works. Not financial advice.
Q2 2026 and Recent Business Highlights
- Reported the first preclinical data from ATR-COSF demonstrating breakthrough repeat-dose distribution, controlled delivery into targeted skin layers and anti-wrinkle activity in ex vivo human skin, supporting advancement toward a planned proof-of-concept clinical study.
- Continued enrollment of the first cohort in the Phase 1/2 clinical trial evaluating ATR-04 for EGFR inhibitor-associated rash.
- Continued advancement of recombinant protein initiatives, including Tobacco Etch Virus (TEV) Protease and T7 RNA Polymerase, expanding the Company's platform into biotechnology research and manufacturing applications.
- Issued CEO Letter to Shareholders detailing Azitra's expanded strategy to leverage its proprietary microbial genetic engineering platform across therapeutics, cosmetic ingredients and biotechnology products.
"The second quarter has marked an exciting evolution for Azitra with the first data from our ATR-COSF program, which provided validation of our strategy to leverage our microbial genetic engineering platform beyond traditional therapeutics," said Francisco Salva, Chief Executive Officer of Azitra. "Combined with the continued advancement of ATR-04 and our recombinant protein initiatives, these accomplishments reflect the breadth of opportunities we are creating in multiple billion dollar markets, including therapeutics, cosmetic ingredients and biotechnology applications."
Salva continued: "Our ATR-COSF program continues to excite our team, as it represents one of the first to demonstrate the wrinkle reducing potential of recombinant filaggrin ingredient in ex vivo human skin. It shows Azitra's ability to translate our cutting edge science into observable benefits for consumers. The ATR-COSF program represents our first step in unlocking meaningful value for shareholders while positioning Azitra at the intersection of synthetic biology, artificial intelligence and next-generation biological manufacturing.
"During the quarter, we also continued enrollment of the first cohort in our Phase 1/2 clinical trial evaluating ATR-04 for EGFR inhibitor-associated rash. With six active clinical sites, including MD Anderson Cancer Center, we remain on track to report topline data from the first cohort around year end. Additionally, we are in the process to open eligibility criteria to other cancer treatment related rashes driven by inhibitors along the same EGFR/KRAS/MEK/ERK pathway. EGFR inhibitor-associated rash remains a significant unmet medical need, affecting an estimated
Salva concluded: "Looking ahead, we remain focused on implementing the strategy outlined in our recent shareholder letter. That includes advancing ATR-COSF toward a planned proof-of-concept clinical study, continuing development of our recombinant protein portfolio, including TEV Protease and T7 RNA Polymerase, and progressing ATR-04 as our lead clinical therapeutic program. We believe these initiatives position Azitra to unlock the full potential of our platform while creating multiple avenues for long-term growth and shareholder value."
Pipeline Achievements and Upcoming Milestones
ATR-COSF - New Consumer Initiative to Improve the Appearance of Fine Lines and Wrinkles
- Results from synthesized filaggrin ingredients, repeat application study on explanted cosmetic surgery skin.
- Announced positive preclinical data demonstrating breakthrough repeat-dose delivery and distribution together with anti-wrinkle activity in ex vivo human skin, supporting advancement toward a planned proof-of-concept cosmetic study evaluating the safety and efficacy of ATR-COSF.
- Human cosmetic application study planned to start in Q3 2026.
ATR-04 – Addressing an Unmet Need for Cancer Patients in a Billion Dollar Market Opportunity
- Continued enrollment of the first cohort of the ongoing Phase 1/2 clinical trial evaluating ATR-04 for the treatment of EGFRi-associated rash.
- Topline data from first cohort of Phase 1/2 trial expected in Q4-2026.
Recombinant Protein Platform
- Announced plans to advance development of its recombinant protein portfolio, including TEV Protease and T7 RNA Polymerase.
- Platform provides opportunity to develop high-quality recombinant proteins for biotechnology research and manufacturing applications, representing potential opportunities to leverage its microbial genetic engineering expertise while broadening its long-term commercial potential.
ATR-12 - Advancing Phase 1b Clinical Trial in Netherton Syndrome
- Consistent with the priorities outlined in the Company's recent shareholder letter, Azitra plans to strategically pause further enrollment in the ongoing Phase 1b study evaluating ATR-12 for Netherton syndrome.
- This decision reflects the Company's disciplined approach to capital allocation and its focus on advancing programs with the greatest near-term opportunities for clinical, commercial and shareholder value creation.
Financial Results for the Quarter Ended June 30, 2026
- Research and Development (R&D) expenses: R&D expenses for the quarter ended June 30, 2026, were
$1.4 million $1.4 million - General and Administrative (G&A) expenses: G&A expenses for the quarter ended June 30, 2026, were
$2.1 million $1.5 million - Net Loss was
$3.3 million $2.9 million - Cash and cash equivalents: As of June 30, 2026, Azitra had cash and cash equivalents of
$6.7 million
About Azitra, Inc.
Azitra, Inc. is a clinical-stage biopharmaceutical company focused on developing innovative therapies for precision dermatology and novel products across therapeutics, cosmeceuticals and biotechnology applications. The Company's portfolio is highlighted by ATR-COSF, a recombinant protein technology designed for cosmetic and skincare applications, and ATR-04, an investigational live biotherapeutic for EGFR inhibitor ("EGFRi") associated rash. Azitra has received Fast Track designation from the FDA for EGFR inhibitor-associated rash, which impacts approximately 150,000 people in the U.S. Azitra is also advancing additional recombinant protein initiatives designed to support biotechnology research and manufacturing applications. Azitra's technology platforms combine engineered proteins, topical live biotherapeutics, artificial intelligence, and a proprietary microbial library to develop differentiated products for consumer, research and healthcare markets. For more information, please visit https://azitrainc.com.
Forward-Looking Statements
This 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 (i) our potential resumption and expected timing of initial safety data and topline results for the Phase 1b trial for our ATR-12, (ii) the abstract detailing the Phase 1/2 clinical trial for our ATR-04 program, (iii) our provision of initial safety data and topline results for the Phase 1/2 clinical trial for our ATR-04 program, (iv) statements about our clinical and preclinical programs, and corporate and clinical/preclinical strategies, including our cosmeceutical strategy and our recombinant protein platform, (v) the expected timing of our planned human cosmetic application study for ATR-COSF, and (vi) statements regarding our strategy plans and priorities, including those outlined in our recent shareholder letter.
Any 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: the timing of clinical trials and their results; we may experience delays in the provision of initial safety data and topline results for ATR-COSF, our recombinant protein platform, ATR-12 and ATR-04 and, if we do, such data and results may not be favorably received; the safety and efficacy of our product candidates; possible 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 or incorporated by reference in our annual report on Form 10-K filed with the United States Securities and Exchange Commission (the "SEC") on February 27, 2026 and our quarterly report on Form 10-Q filed on May 13, 2026 and August 12, 2026 with the SEC. Azitra explicitly disclaims any obligation to update any forward-looking statements except to the extent required by law.
Contact
Norman Staskey
Chief Financial Officer
staskey@azitrainc.com
Investor Relations
Tiberend Strategic Advisors, Inc.
David Irish
231-632-0002
dirish@tiberend.com
Media Relations
Tiberend Strategic Advisors, Inc.
Casey McDonald
646-577-8520
cmcdonald@tiberend.com
Condensed Statement of Operations | ||||||||
(Unaudited) | ||||||||
Three Months Ended June 30, | ||||||||
2026 | 2025 | |||||||
Operating expenses: | ||||||||
General and administrative | $ | 2,067,639 | $ | 1,469,513 | ||||
Research and development | 1,351,529 | 1,401,839 | ||||||
Total operating expenses | 3,419,168 | 2,871,352 | ||||||
Loss from operations | 3,419,168 | 2,871,352 | ||||||
Other income (expense): | ||||||||
Interest income | 74,661 | 15,461 | ||||||
Interest expense | (1,365) | (468) | ||||||
Change in fair value of warrants | — | 54 | ||||||
Other income | (1,788) | (32,688) | ||||||
Total other income (expense) | 71,508 | (17,641) | ||||||
Loss before income taxes | 3,347,660 | 2,888,993 | ||||||
Income tax expense | — | — | ||||||
Net loss | $ | 3,347,660 | $ | 2,888,993 | ||||
Net loss per Share, basic and diluted | $ | (0.17) | $ | (1.18) | ||||
Weighted average common stock outstanding, basic and diluted | 19,300,704 | 2,444,340 | ||||||
Condensed Balance Sheets | ||||||||
Unaudited | ||||||||
June 30, | December 31, | |||||||
2026 | 2025 | |||||||
Assets | ||||||||
Current Assets: | ||||||||
Cash and cash equivalents | $ | 6,727,810 | $ | 2,068,083 | ||||
Other receivables | 144,730 | 141,295 | ||||||
Prepaid expenses and other current assets | 571,282 | 809,949 | ||||||
Total current assets | 7,443,822 | 3,019,327 | ||||||
Property and equipment, net | 536,422 | 548,591 | ||||||
Other assets | 935,802 | 1,457,468 | ||||||
Total assets | $ | 8,916,046 | $ | 5,025,386 | ||||
Liabilities and stockholders' equity | ||||||||
Current liabilities: | ||||||||
Accounts payable | $ | 497,985 | $ | 399,356 | ||||
Current financing lease liability | 1,486 | 10,111 | ||||||
Current operating lease liability | 357,569 | 255,776 | ||||||
Insurance premium financing liability | — | 198,983 | ||||||
Accrued expenses | 673,669 | 203,740 | ||||||
Total current liabilities | 1,530,709 | 1,067,966 | ||||||
Long-term operating lease liability | 50,998 | 156,190 | ||||||
Total liabilities | 1,581,707 | 1,224,156 | ||||||
Stockholders' equity | ||||||||
Common stock | 6,060 | 1,074 | ||||||
Additional paid-in capital | 83,124,375 | 72,321,352 | ||||||
Accumulated deficit | (75,796,096) | (68,521,196) | ||||||
Total stockholders' equity | 7,334,339 | 3,801,230 | ||||||
Total liabilities and stockholders' equity | $ | 8,916,046 | $ | 5,025,386 | ||||
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SOURCE Azitra, Inc.