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DBV Technologies Reports Third Quarter 2026 Financial Results and Business Update

Globe Newswire•28/10/2026•16:47 ET
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Key Highlights

  • ➤BLA submitted for VIASKIN Peanut Patch in children aged 4-7; Priority Review requested
  • ➤Cash and equivalents $165.7 million at September 30, funding operations into Q3 2027
  • ➤Net loss $64.5 million in Q3 2026 versus $33.2 million in Q3 2025
  • ➤$50 million gross ADS sale completed under the ATM program
  • ➤FDA Priority Review and substantive-review determination expected in Q4 2026

Expert Statements

Daniel Tassé, Chief Executive Officer of DBV Technologies

“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”

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.”

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.”

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