DBV Technologies Reports Third Quarter 2026 Financial Results and Business Update
Nine-month operating and investing cash use reached $159.4 million, compared with $86.7 million a year earlier.
Sentiment and the balance of points
Rhea-AI Sentiment reads the wording of the document, how positive or negative its language is on a 1 to 5 scale. The balance of points shown with the takes weighs what the document actually discloses, so the two can disagree, for example when a trial that missed its main goal is described in upbeat language.
Rhea-AI Summary
DBV Technologies (DBVT) reported a third-quarter net loss of $64.5 million while advancing its VIASKIN Peanut Patch regulatory application. The loss widened from $33.2 million a year earlier. Cash and cash equivalents were $165.7 million at September 30, 2026; DBV estimates funding into the third quarter of 2027, but disclosed substantial doubt about its ability to continue as a going concern.
The company submitted its U.S. marketing application for children aged 4 through 7 on September 29, 2026, requesting Priority Review. FDA's filing-acceptance and Priority Review decisions are expected in the fourth quarter of 2026. DBV expects to submit its application for toddlers aged 1 through 3 in 2027. It also completed a $50 million gross ADS sale to RA Capital Management and refreshed its $150 million at-the-market share-sale program. Commercial preparations continued for a potential launch, subject to approval.
How this balance works
Rhea-AI gives every point it takes from this document a weight. Minor counts 1, Moderate 3 and Major 9, so one Major point outweighs several Minor ones. The bar adds up the weights on each side, and when neither side holds more than 65% of the total the balance reads Mixed.
It reads the document as published, with the same rules for every company, and it does not look at what the market expected or at how the stock traded, so a point can be objectively good on a day the stock falls.
Rhea-AI Sentiment measures something else, the tone of the wording.
Hollow bars mark forward-looking points. How the balance works
Positive
- Moderate pointVIASKIN Peanut Patch application for children aged 4 through 7 submitted September 29, 2026, with Priority Review requested.
- Moderate pointADS sale to RA Capital Management raised $50 million in gross proceeds. 7.9% of market cap
- Moderate pointAt-the-market share-sale program refreshed at $150 million. 24% of market cap
- Moderate point. Forward-looking: it has not happened yet and may not happen.Existing cash of $165.7 million at September 30, 2026, is estimated to fund operations into Q3 2027.
- Minor point. Forward-looking: it has not happened yet and may not happen.Toddler application for children aged 1 through 3 is expected to be submitted in 2027.
4 minor points
- Minor pointCommercial readiness advanced through U.S. launch infrastructure, distribution and specialty pharmacy selection.
- Minor pointClinical development advanced the COMFORT Toddlers and THRIVE programs.
- Minor pointNet loss per share narrowed to $0.14 in Q3 and $0.37 over nine months, versus $0.24 and $0.82, respectively, in 2025.
- Minor pointNine-month financial income increased to $1.5 million from nil in 2025.
Negative
- Major pointSubstantial going-concern doubt exists; cash is not expected to fund twelve months from financial-statement issuance.
- Moderate pointAdditional capital is required; financing availability and terms depend on regulatory developments and market conditions.
- Moderate pointNet loss widened to $64.5 million in Q3 and $162.5 million over nine months, versus $33.2 million and $102.1 million in 2025.
- Moderate pointOperating and investing cash use rose to $159.4 million over nine months, versus $86.7 million in 2025.
- Moderate pointThe $50 million ADS sale issued additional equity, diluting existing holders. 7.9% of market cap
8 minor points
- Minor pointR&D expenses rose to $47.0 million in Q3 and $111.6 million over nine months, versus $28.6 million and $83.8 million in 2025.
- Minor pointSales and marketing expenses rose to $5.3 million in Q3 and $15.7 million over nine months, versus $1.2 million and $1.9 million in 2025.
- Minor pointG&A expenses rose to $14.0 million in Q3 and $39.1 million over nine months, versus $7.3 million and $21.3 million in 2025.
- Minor pointResearch-tax-credit operating income fell to $1.6 million in Q3 and $3.1 million over nine months, versus $2.8 million and $5.0 million in 2025.
- Minor pointQ3 financial income declined to $0.6 million from $1.1 million in 2025.
- Minor pointIncome tax expense increased to $0.3 million in Q3 and $0.7 million over nine months, versus nil and $0.1 million in 2025.
- Minor pointFDA filing acceptance and Priority Review remain pending, with decisions expected in Q4 2026.
- Minor point. Forward-looking: it has not happened yet and may not happen.Potential VIASKIN Peanut Patch commercialization remains subject to approval.
News Explained
The completed ADS sale reduces existing holders’ percentage ownership, and the BLA’s planned inspection follows Fareva’s expected completion of remediation.
The company completed a
Fareva is continuing remediation activities following the
Key Figures
- VITESSE enrollment
- 654 children
- Phase 3 trial supporting the BLA
- FDA review determination
- Fourth quarter of 2026
- Expected determination on filing acceptance and whether Priority Review is granted
- Cash and cash equivalents
- $165.7 million
- As of September 30, 2026
- Cash runway
- Into the third quarter of 2027
- Company estimate based on current operations, plans and assumptions
- ADS sale gross proceeds
- $50 million
- Completed sale to RA Capital Management
- ATM program
- $150 million
- Refreshed program
- Net loss
- $64.5 million vs. $33.2 million
- Third quarter 2026 vs. third quarter 2025
- Net loss
- $162.5 million vs. $102.1 million
- Nine months ended September 30, 2026 vs. 2025
Previous Earnings Reports
-
Reported BLA timing anticipated the current submission; cash runway was also projected into Q3 2027.
-
Reported nine-month net loss and cash position provide a year-earlier financial comparison for this Q3 update.
24h Move is the share-price change in the day after each event; other market factors may also have contributed.
Key Terms
biologics license application regulatory
priority review regulatory
atm program financial
pre-approval inspection regulatory
going concern financial
AI-generated analysis. How Rhea-AI works. Not financial advice.
Châtillon, France, October 28, 2026
DBV Technologies Reports Third Quarter 2026 Financial Results and Business Update
- Submitted the Biologics License Application to U.S. FDA for the VIASKIN® Peanut Patch in children aged 4-7 Years and requested Priority Review
- Accelerated Commercial Readiness towards the launch of the VIASKIN® Peanut Patch in children aged 4-7 years in the US, if approved
- Reported cash and cash equivalents of
$165.7 million as of September 30, 2026, funding into third quarter of 2027 - DBV will host a conference call today, October 28, at 5:00pm ET
DBV Technologies (Euronext: DBV – ISIN: FR0010417345 – Nasdaq Stock Market: DBVT – CUSIP: 23306J309), a late-stage specialty biopharmaceutical company, today reported financial results for the Third Quarter of 2026. The quarterly and nine months financial statements were approved by the Board of Directors on October 28, 2026.
“The third quarter marked a defining step in DBV’s evolution from a clinical-stage company into a commercial organization. With our BLA now submitted for children aged 4 through 7 years, and our planned BLA in toddlers aged 1 through 3 years, we are concentrating our efforts on the areas that will advance the company most meaningfully,” said Daniel Tassé, Chief Executive Officer of DBV Technologies. “We are grateful for the productive, ongoing dialogue with the FDA about both BLAs. As the regulatory dialogue progresses, we have every function across the company aligned on supporting a complete and efficient review of both dossiers, advancing manufacturing readiness alongside our contract manufacturing partner, and preparing to execute our launch plans with discipline.”
Third Quarter 2026 Operational Highlights and 2027 Business Updates
Regulatory Execution
- Submitted the Biologics License Application to U.S. FDA for the VIASKIN® Peanut Patch in children aged 4 through 7 Years and requested Priority Review.
- The BLA is supported by the Phase 3 VITESSE trial, which enrolled 654 children and is the largest immunotherapy trial to date in this population.
Corporate and Financial Position
- Funded into the third quarter of 2027, enabling continued execution through the regulatory review process and commercial preparedness, including continued investment across core functions required to potentially launch and support the long-term success of the VIASKIN® Peanut Patch brand, including Medical Affairs, Sales, Market Access, Marketing, Account Management, and Pharmacovigilance.
- Refreshed the Company’s
$150 million ATM program and completed$50 million of gross proceeds sale of ADSs to RA Capital Management.
Manufacturing Progress
- Continued working closely with Fareva Amboise (Fareva), the Company’s contract manufacturing organization, on remediation activities following the April 2026 FDA Warning Letter to Fareva.
- Maintained a direct line of sight into remediation work specific to the VIASKIN® Peanut Patch production, which is led by external specialists against a detailed project plan shared by Fareva with DBV.
- Received confirmation from Fareva that it has responded to FDA in accordance with regulatory timelines and has provided monthly updates to the Agency.
- Based on ongoing collaboration with Fareva, a target date for the Pre-Approval Inspection (PAI) was included in the BLA, in line with FDA regulations and standard industry practices.
- The target date for the PAI falls after the date by which Fareva expects to complete remediation.
Toddler Program
- DBV has held discussions with the Agency on how to ensure a timely review of the BLA for toddlers aged 1 through 3 years following the recent submission of the 4-through-7 BLA, including a potential rolling submission of the 1-through-3 BLA. The same review Team will review both BLAs. FDA indicated that a review of the 1-through-3 BLA initiated shortly after the review of the 4-through-7 BLA would allow the Agency to build on the learnings from their review and the efficiencies expected from the meaningful content overlap of the two BLAs. It would provide DBV and FDA the opportunity to align on the form, content, and best timing of the components of the 1-through-3 BLA submission, in support of an efficient review of both BLAs.
- DBV will continue the regulatory dialogue with FDA over the next few months and expects to submit the toddler BLA in 2027. DBV will provide an update once the FDA discussions regarding the Company’s toddler program have been finalized.
Upcoming Milestones
- File acceptance for the BLA in children aged 4 through 7 years. Determination by FDA whether the BLA for children aged 4 through 7 years is sufficiently complete to begin the full substantive review, including whether Priority Review is granted, expected in the fourth quarter of 2026.
Financial Highlights for the Third Quarter Ended September 30, 2026
The Company’s interim unaudited condensed consolidated financial statements for the three and nine months ended September 30, 2026, and the comparative period of September 30, 2025, are prepared in accordance with accounting principles generally accepted in the United States (“U.S. GAAP”).
Operating Income
Operating income was
Operating Expenses
Research and Development Expenses
R&D expenses were
- Submitted the BLA for the VIASKIN® Peanut Patch for children aged 4 through 7 years on September 29, 2026, and advanced COMFORT Toddlers and THRIVE.
- Recorded
$4.7 million of BLA filing fees. - Continued investment in launch capabilities and maintained the build of precommercial inventory, for
$4.5 million for the 3 months and$10.2 million for the first nine months of 2026 to support a potential successful launch of the VIASKIN® Peanut Patch, if approved.
Sales and Marketing Expenses
Sales and marketing expenses were
- Continued execution of U.S. launch readiness, with the commercial organization expanding
- Advanced launch infrastructure, including distribution and specialty pharmacy selection
General and Administrative (“G&A”) Expenses
G&A expenses were
The increase reflects continued scaling of the corporate infrastructure supporting potential commercialization across core functions including Medical Affairs, Sales, Market Access, Marketing, Account Management, and Pharmacovigilance.
Financial Income (Expense)
Financial income was
Income Tax
Income tax expense was
Net Loss and Net Loss Per Share
Net loss was
Cash Position and Liquidity
These condensed consolidated financial statements have been prepared assuming that the Company will continue as a going concern.
The Company has incurred operating losses and negative cash flows from operations since inception and expects operating cash outflows to remain significant as it continues to invest in clinical development, regulatory activities, manufacturing and supply-chain readiness and preparations for the potential commercialization of the VIASKIN® Peanut Patch, if approved. Net cash used in operating & investing activities was
As of September 30, 2026, the Company had cash and cash equivalents of
Management has concluded that the Company's existing cash and cash equivalents are not expected to be sufficient to fund its operations for at least twelve months from the date of issuance of these condensed consolidated financial statements. Accordingly, substantial doubt exists about the Company's ability to continue as a going concern within twelve months after the date these condensed consolidated financial statements are issued.
The Company will require additional capital to fund its operations. Management is actively evaluating multiple financing alternatives, including without limitation, potential additional sales under the Company’s existing ATM Program, equity transactions, warrants exercise and other alternative forms of financing. The Company’s continued advancement through the regulatory review process may provide additional financing opportunities. However, the availability, timing and terms of any additional financing will depend on regulatory developments, market conditions and investors’ interest, lenders and other counterparties, and there can be no assurance that additional financing will be available when needed, on acceptable terms or at all.
These estimates are based on the Company’s current forecasts and exclude additional expenditure related to programs other than VIASKIN® Peanut patch or resulting from the potential in-licensing or acquisition of additional product candidates or technologies. The timing and amount of the Company’s future cash requirements may differ materially from current estimates depending on, among other factors, the timing and outcome of the regulatory review process, the pace of clinical development activities, manufacturing and supply-chain commitments, commercial readiness activities and foreign exchange rate fluctuations. These condensed consolidated financial statements do not include any adjustments to the carrying amounts and classification of assets and liabilities or reported expenses that may be necessary if the Company were unable to continue as a going concern.
Conference Call & Webcast
DBV management will host an investor conference call and webcast today, October 28th at 5:00pm ET, to discuss this update. This call is accessible via the below teleconferencing numbers and requesting the DBV Technologies call.
United States: +1-877-344-8082
International: +1-213-992-4618
A live webcast of the call will be available on the Events section of the Company’s website here.
UNAUDITED CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
| In millions of USD (unaudited) | U.S. GAAP | U.S. GAAP | ||
| Nine months ended September 30, | Three months ended September 30, | |||
| 2026 | 2025 | 2026 | 2025 | |
| Operating income | 3.1 | 5.0 | 1.6 | 2.8 |
| Research & Development | (111.6) | (83.8) | (47.0) | (28.6) |
| Sales & Marketing | (15.7) | (1.9) | (5.3) | (1.2) |
| General & Administrative | (39.1) | (21.3) | (14.0) | (7.3) |
| Operating expenses | (166.4) | (107.0) | (66.3) | (37.1) |
| Financial income/(expense) | 1.5 | — | 0.6 | 1.1 |
| Income tax | (0.7) | (0.1) | (0.3) | — |
| Net loss | (162.5) | (102.1) | (64.5) | (33.2) |
| Basic/diluted net loss per share attributable to shareholders | ||||
About DBV Technologies
DBV Technologies is a late-stage biopharmaceutical company developing treatment options for food allergies and other immunologic conditions with significant unmet medical need. DBV Technologies is currently focused on investigating the use of its proprietary VIASKIN® patch technology to address food allergies, which are caused by a hypersensitive immune reaction and characterized by a range of symptoms varying in severity from mild to life-threatening anaphylaxis. Millions of people live with food allergies, including young children. Through epicutaneous immunotherapy (EPIT), the VIASKIN® Peanut Patch is designed to introduce microgram amounts of a biologically active compound to the immune system through intact skin. EPIT is a new class of non-invasive treatment that seeks to modify an individual’s underlying allergy by re-educating the immune system to become desensitized to allergen by leveraging the skin’s immune tolerizing properties. DBV Technologies is committed to transforming the care of people with food allergies. The Company’s food allergy programs include ongoing clinical trials of VIASKIN® Peanut Patch in toddlers (1 through 3 years of age) and children (4 through 7 years of age) with peanut allergy.
DBV Technologies is headquartered in Châtillon, France, with North American operations in Warren, NJ. The Company’s ordinary shares are traded on segment B of Euronext Paris (DBV, ISIN code: FR0010417345) and the Company’s ADSs (each representing five ordinary shares) are traded on the Nasdaq Capital Market (DBVT – CUSIP: 23306J309).
For more information, please visit www.dbv-technologies.com and engage with us on X (formerly Twitter) and LinkedIn.
Forward Looking Statements
This press release may contain forward-looking statements and estimates, including statements regarding DBV’s financial condition, forecast of its estimated cash runway into the third quarter of 2027, DBV’s ability to obtain additional capital to fund its operations and the substantial doubt regarding DBV”s ability to continue as a going concern, the therapeutic potential of VIASKIN® Peanut patch and EPIT, DBV’s planned regulatory and clinical efforts including timing and results of communications with regulatory agencies, timing and expectations with respect to FDA determination on whether the BLA for VIASKIN® Peanut Patch for peanut allergic children 4 through 7 years of age is sufficiently complete for substantive review, plans, timing, and expectations with respect to priority review of the BLA for VIASKIN® Peanut Patch for peanut allergic children 4 through 7 years of age; timing and expectations with respect to Pre-Approval Inspection of Fareva, timing and expectations related to Fareva’s Warning Letter remediation efforts; expectations regarding timing of BLA submission for VIASKIN® Peanut patch in toddlers aged 1 through 3 years; the continued advancement of the VIASKIN® Peanut patch in toddlers aged 1 through 3 year, DBV’s commercial launch preparedness activities and the build-out of its commercial infrastructure in the United States, and the ability of any of DBV’s product candidates, if approved, to improve the lives of patients with food allergies. These forward-looking statements and estimates are not promises or guarantees and involve substantial risks and uncertainties. At this stage, DBV’s product candidates have not been authorized for sale in any country. Among the factors that could cause actual results to differ materially from those described or projected herein include uncertainties associated generally with research and development, clinical trials and related regulatory reviews and approvals, DBV’s ability to raise additional capital and continue as a going concern, and DBV’s ability to successfully execute on its budget discipline measures. A further list and description of risks and uncertainties that could cause actual results to differ materially from those set forth in the forward-looking statements in this press release can be found in DBV’s regulatory filings with the U.S. Securities and Exchange Commission (“SEC”), including in DBV’s Annual Report on Form 10-K for the year ended December 31, 2025, filed with the SEC on March 26, 2026, as amended by the Amendment No. 1 on Form 10-K/A filed with the SEC on April 30, 2026, DBV’s Quarterly Report on Form 10-Q filed with the SEC on October 28, 2026, and future filings and reports made with the SEC by DBV. Existing and prospective investors are cautioned not to place undue reliance on these forward-looking statements and estimates, which speak only as of the date hereof. Other than as required by applicable law, DBV Technologies undertakes no obligation to update or revise the information contained in this Press Release.
VIASKIN is a registered trademark of DBV Technologies.
Investor Contact
Virginie Boucinha
DBV Technologies
virginie.boucinha@dbv-technologies.com
Media Contact
Brett Whelan
DBV Technologies
brett.whelan@dbv-technologies.com
Attachment
FAQ
AI-generated questions and answers. How Rhea-AI works. Not financial advice.
What were DBV Technologies' third-quarter 2026 financial results?
DBV reported a $64.5 million net loss for the third quarter of 2026, compared with $33.2 million in the third quarter of 2025. Net loss per share was $0.14, compared with $0.24. Cash and cash equivalents totaled $165.7 million at September 30, 2026.
When does DBV expect FDA decisions on its VIASKIN Peanut Patch application?
FDA's decisions on filing acceptance and whether to grant Priority Review for children aged 4 through 7 are expected in the fourth quarter of 2026. Filing acceptance determines whether the application is sufficiently complete for substantive review; it is not marketing approval.
What spending is excluded from DBV Technologies' cash runway estimate?
The estimate excludes additional spending on programs other than the VIASKIN Peanut Patch and spending resulting from potential in-licensing or acquisitions of additional product candidates or technologies. DBV bases its estimate on current operating forecasts and milestone-based spending assumptions.