Item 8.01. Other Events

On January 14, 2021, DBV Technologies S.A. (the "Company") issued a press release announcing the Company's receipt from the U.S. Food and Drug Administration ("FDA") of written responses to questions provided in the Type A meeting request the Company submitted in October 2020. The Type A meeting request was submitted following the Company's receipt of a Complete Response Letter from the FDA in connection with the Company's Biologics License Application for Viaskin™ Peanut (DBV712), an investigational, non-invasive, once-daily epicutaneous patch to treat peanut allergy in children ages 4 to 11 years. A copy of the Company's press release is attached hereto as Exhibit 99.1 and is incorporated by reference herein.

Item 9.01 Financial Statements and Exhibits




(d) Exhibits



            Exhibit No.   Description

            99.1            Press Release, dated January 14, 2021.

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