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Press releaseGlobeNewswire· March 26, 2026

DBV Technologies Reports Full Year 2025 Financial Results and Business Update

View original at globenewswire.com
“Reported cash and cash equivalents of $194 million as of December 31, 2025, plus additional gross proceeds of $94 million received on January 16, 2026”
Verbatim excerpt from the source · GlobeNewswire · short snapshot — read the full document at the original

What we drew from this source

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  • BLA submission for 4-7 year olds anticipated in the first half of 2026 with potential for Priority Review

    60% confidence
  • Cash and cash equivalents are sufficient to fund operations into the second quarter of 2027

    60% confidence
  • Completion of enrollment of COMFORT Toddlers safety study and subsequent topline results readout expected in 2026

    60% confidence
  • Our focus on bringing the VIASKIN Peanut Patch to peanut-allergic children ages 1-7 years remains unwavering

    60% confidence
  • I am pleased with our progress to date in enhancing DBV's capabilities and building a company ready for launch

    60% confidence
  • We entered 2025 with a clear set of priorities – strengthening our financial position, advancing our clinical development program (including completing VITESSE and initiating COMFORT Toddlers), and preparing for the BLA submission and commercialization of the VIASKIN Peanut Patch in the United States, if approved

    60% confidence
  • BLA submission for 1-3 year olds anticipated in the second half of 2026 under an Accelerated Approval Pathway

    60% confidence

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Q4 2026 Biotech Catalyst Window: ESMO Data, the Ivonescimab PDUFA and Small-Cap Delistings
Mid-October to November 2026 is a dense catalyst period for clinical-stage biotech. Positive late-stage readouts (ALOFT-IPF, TELIGAN, MIUDELLA, the duvakitug extension) and the ESMO 2026 presentations lead up to the FDA's 14 November PDUFA date for the ivonescimab BLA. At the opposite end of the market, Spago Nanomedical is moving to delist from Nasdaq First North, which shows how hard it is for micro-cap developers to fund themselves. Value is concentrating in companies with late-stage data and near-term regulatory outcomes.
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EPKINLY Regulatory-Clinical Success Cascade
High probability of expanded label indications, additional combination approvals, and competitive positioning strength in follicular lymphoma market. Predicts positive commercial uptake and potential accelerated review for related indications.
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Where sources disagree
Ford Motor Company
Both facts give cash for Ford Motor Company at the same point in time (2025-12-31; FY 2025 year-end and Q4 2025 year-end are the same date). Both are labelled USD, but the values are 23,356,000,000 and 23.356, which cannot both be true in USD. The two numbers agree once the second is read as billions (23.356 bn = 23,356,000,000), so the economic content is consistent and the conflict is a unit/scale error in the Q4 2025 record. The period is not the reason for the conflict: a Q4 and an FY figure at the same year-end date should match.
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