DBV Technologies Completes Screening for the VITESSE Phase 3 Clinical Trial
September 23 2024 - 3:30PM
Châtillon, France, September 23, 2024
DBV Technologies Completes Screening for
the VITESSE Phase 3 Clinical Trial
- In Q3 2024, DBV exceeded
its recruitment goal and successfully closed the screening process
for the VITESSE Phase 3 study evaluating the
Viaskin® Peanut Patch in peanut
allergic children ages 4 – 7 years old
- Topline results of VITESSE
data are expected by Q4 2025
DBV Technologies (Euronext: DBV – ISIN:
FR0010417345 – Nasdaq Stock Market: DBVT), a clinical-stage
biopharmaceutical company, today announced that patient screening
is complete for the Phase 3 trial, VITESSE
(Viaskin Peanut Immunotherapy
Trial to Evaluate
Safety, Simplicity and
Efficacy), using the modified Viaskin Peanut Patch
in children ages 4 – 7 years old with peanut allergy.
“We are thrilled to have reached this
significant milestone,” said Dr. Pharis Mohideen, Chief
Medical Officer of DBV Technologies. “VITESSE is by
far the largest immunotherapy clinical trial for this patient
population. I cannot thank our study centers enough for their
dedication and commitment to DBV’s Viaskin® peanut patch program.
Of course, none of this is possible without our subjects and their
supportive families. Being in a clinical trial takes a tremendous
amount of time, and we are grateful that subjects are willing to
make this sacrifice to further treatments in food allergy. I’m
delighted that we closed screening in August, a month earlier than
anticipated. I am particularly pleased with our success in reaching
out to the diverse communities that suffer from peanut allergies in
this trial. DBV continues to focus on advancing this important
development program to support a Biologic License Application
submission. We look forward to continued collaboration with our
shared stakeholders as we move ahead.”
The fully enrolled VITESSE Phase 3 trial in
peanut-allergic children ages 4 – 7 is a 12-month study evaluating
the efficacy and safety of the Viaskin Peanut Patch in more than
600 subjects (randomized 2:1), representing individuals across 86
sites in the U.S., Canada, Europe, the UK, and Australia. VITESSE
is currently the largest treatment intervention study in peanut
allergy.
About DBV TechnologiesDBV
Technologies is a clinical-stage biopharmaceutical company
developing treatment options for food allergies and other
immunologic conditions with significant unmet medical need. DBV is
currently focused on investigating the use of its proprietary
technology platform, Viaskin, 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 platform 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 is committed to
transforming the care of food allergic people. The Company’s food
allergy programs include ongoing clinical trials of Viaskin Peanut
in peanut allergic toddlers (1 through 3 years of age) and children
(4 through 7 years of age).
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 (Ticker:
DBV, ISIN code: FR0010417345) and the Company’s ADSs (each
representing one ordinary share) are traded on the Nasdaq Capital
Select Market (Ticker: DBVT).
For more information, please visit
www.dbv-technologies.com and engage with us on X (formerly Twitter)
and LinkedIn.
Forward Looking StatementsThis
press release may contain forward-looking statements and estimates,
including statements regarding DBV’s financial condition, forecast
of its cash runway, the therapeutic potential of Viaskin® Peanut
patch and EPIT™, designs of DBV’s anticipated clinical trials,
DBV’s planned regulatory and clinical efforts including timing and
results of communications with regulatory agencies, 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, 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 French Autorité des Marchés
Financiers (“AMF”), DBV’s filings and reports 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, 2023,
filed with the SEC on March 7, 2024, and future filings and reports
made with the AMF and 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 and EPIT is a
trademark of DBV Technologies.
Investor Contact Katie
MatthewsDBV Technologieskatie.matthews@dbv-technologies.com
Media ContactAngela MarcucciDBV
Technologiesangela.marcucci@dbv-technologies.com
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