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NCT03861455CompletedPhase 2

Efficacy and Safety of Dupilumab Chronic Hands Eczema Refractory to Highly Potent Topical Corticosteroids

DUPECZEMAIN : Double Blind Placebo-controlled Randomized Multicenter Study Assessing the Efficacy and Safety of Dupilumab in Moderate to Severe Chronic Hands Eczema Refractory to Highly Potent Topical Corticosteroids

Source: ClinicalTrials.gov · Last updated 3 Dec 2024

Brief summary (registry, in English)

Dupilumab has recently demonstrated high efficacy and good safety profile in the treatment of moderate-to-severe atopic dermatitis. There is a crucial need of developing new treatment options in Chronic hand eczema refractory to topical therapy. Investigators hypothesise that Dupilumab will also have high efficacy and good safety profile in the treatment of moderate to severe Chronic hand eczema refractory to highly potent topical corticosteroids.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
94 (actual)
First submitted
28 Nov 2018
Start date
15 Jul 2019
Primary completion date
9 Nov 2023
Lead sponsor
University Hospital, Toulouse
NCT number
NCT03861455
EudraCT number
2018-002830-19

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 94
  • From 15 Jul 2019 to the primary completion date, 9 Nov 2023
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Treatment with topical corticosteroids or topical calcineurin inhibitors within one week of baseline.
  • Treatment with oral immunosuppressants (including cyclosporine, methotrexate, azathioprine, mycophenolate mofetil), alitretinoin or phototherapy within 4 weeks of baseline visit.
  • Treatment with an investigational drug within 8 weeks (or 5 half-lives) of baseline.
  • Active chronic infection requiring the use of a systemic antibiotic within 2 weeks before study start.

Other illness

  • Hypersensitivity to dupilumab or to any of its ingredients
  • Any other condition (e;g., psoriasis) on the hands that according to the investigator will impair the ability to evaluate treatment effect.
  • Known or suspected history of immunosuppression, including history of invasive opportunistic infections (e.g., tuberculosis, histoplasmosis, listeriosis, coccidioidomycosis, pneumocystis, aspergillosis) despite infection resolution; or unusually frequent, recurrent, or prolonged infections, per investigator judgment.
  • History of human immunodeficiency virus (HIV) infection or positive HIV serology at screening.
  • Positive for hepatitis B surface antigen, hepatitis B core antibody, or hepatitis C antibody at the screening visit.
  • Patients with known helminth infections.

Other

  • Patients under adult autonomy protection system
  • Pregnant or breastfeeding women, or women planning to become pregnant or breastfeed during the study. Women of childbearing potential who are sexually active and unwilling to use an adequate birth control method

Who the study is looking for

  • Patients affiliated to a social insurance protection regimen.
  • Patients with moderate to severe chronic (\>6 months) hand eczema with an Investigator global assessment (IGA) of 3 or 4 (out of a scale of 0 to 4).
  • Patients intolerant (according to the physician) or resistant to highly potent topical corticosteroids. Inadequate response (resistance) to highly potent topical corticosteroids is defined as a history of failure to achieve and maintain remission or a low disease activity state (comparable to an IGA score of 0 \[indicating clear\] to 2 \[indicating mild\]) despite treatment with a daily regimen of highly potent topical corticosteroids applied for 14 days or for the maximum duration recommended for highly potent topical corticosteroids.
  • Patients who are able to understand the study procedures including the ability to complete patient-oriented questionnaires.
  • Patients who are able to apply a stable dose of emollients within 7 days before the baseline visit.
  • Patients who agree to sign the written informed consent.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Saint André Hospital
Coordinator of this site? Confirm its status
BordeauxFranceUnknown status
Hôpital Saint Eloi
Coordinator of this site? Confirm its status
MontpellierFranceUnknown status
CHU Lyon-Sud Département d'allergologie et d'immunologie clinique
Coordinator of this site? Confirm its status
Pierre-BéniteFranceUnknown status
Larrey Hospital
Coordinator of this site? Confirm its status
ToulouseFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.