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Expanded Access Protocol of Viaskin® Peanut (DBV712) in Peanut-allergic Children

Viaskin® Peanut (DBV712) Compassionate Use in Peanut-allergic Children Previously Enrolled in a DBV712 Clinical Study

Status
AVAILABLE
Phases
Unknown
Study type
Expanded Access
Source
ClinicalTrials.gov
Registry ID
NCT05424731
Enrollment
Unknown
Registered
2022-06-21
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Peanut Allergy

Keywords

EPIT, Epicutaneous, Immunotherapy, Viaskin

Brief summary

This is an open label expanded access program for male and female patients 2 years or older, to provide continued desensitization treatment with DBV712 250 mcg.

Detailed description

This study is an open-label Expanded Access Protocol to provide continued treatment with DBV712 for individuals completing a DBV clinical study. Participation is by invitation according to the inclusion criteria. For individuals who have received DBV712 for longer than one year prior to entry into this protocol, where treatment allocation is unblinded, safety assessment and resupply of DBV712 will occur at 6-month intervals. There will be no other scheduled study visits. For individuals who have been on blinded treatment, a safety assessment will be conducted at Months 1 and 3. Visits for safety assessment and resupply of DBV712 will occur at 3-month intervals during the first 12 months. After a year, visits will occur at 6-month intervals. DBV712 will be supplied to participants at study visits to suffice until the next visit. For individuals who have been on blinded treatment, or off DBV712 treatment for more than 14 days prior to entry into this protocol, dosing consists of approximately 6 hours for the first week, 12 hours for the second week, then once daily, at approximately the same time of day. Treatment with DBV712 will continue until, in the clinical judgement of the treating physician, the participant is no longer benefiting from continuation of the treatment, DBV712 is approved and available by prescription, or the study is terminated.

Interventions

COMBINATION_PRODUCTDBV712 250 mcg

Daily epicutaneous delivery.

Sponsors

DBV Technologies
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
ALL
Age
2 Years to 17 Years

Inclusion criteria

* Participation is by invitation, limited to individuals completing clinical study V712-303 (PEOPLE), previous Expanded Access Program or a DBV clinical study initiated after 31-Jan-2022 * Male and females; ages ≥ 2 years old at Visit 1 or current or prior studies. * Negative urine pregnancy test for female participants of childbearing potential.

Exclusion criteria

* Early withdrawal from a DBV712 clinical study. * History of non-compliance during the primary clinical study or unable to follow the protocol requirements. * Generalized dermatologic disease extending widely on the skin. * History of intolerance or who developed hypersensitivity to excipients of the DBV712 patches.

Countries

United States

Contacts

Primary ContactAnne B Cropp, Pharm. D.
DBV712.eap@earlyaccesscare.com1-888-441-793
Backup ContactLaurie Reynolds, BS
DBV712.eap@earlyaccesscare.com1-888-441-793

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026