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AliCsa; Efficacy of oral alitretinoin versus oral cyclosporine in patients with moderate to very severe hand eczema. A randomized prospective open-label trial with blinded outcome assessment
EU CTIS ID: 2024-515140-23-00
What this study is testing
To compare the efficacy of alitretinoin and cyclosporine in patients with moderate to very severe hand eczema.
- Therapeutic use (Phase IV)
A plain-language read of the study's public EU CTIS listing. The study team confirms the details.
Who can take part
You may be able to join if
- • Age ≥ 18 years and ≤ 75 years
- • Moderate, severe or very severe hand eczema for a minimum duration of 3 months as defined by a Physician Global Assessment (PGA) using a validated Photoguide (16), including all clinical types of hand eczema as defined by the Danish Contact Dermatitis Group
- • Refractory to standard therapy, defined as: o Patients received treatment with topical corticosteroids of class II or higher for at least 8 weeks within 3 months before enrolment, with either no response or a transient response o Patients had also received standard skin care, including emollients and barrier protection as appropriate, without significant improvement o Patients had avoided irritants and contact allergens, if identified, without significant improvement
- • Women of childbearing potential are required to use at least two forms of contraception for at least 1 month before starting treatment, during treatment, and for at least 1 month after finishing treatment; these women are required to take monthly pregnancy tests
- Able to provide written Informed Consent
- Able to speak and read the Dutch language
You likely can't join if
- General criteria prior to randomization • Treated with alitretinoin or cyclosporine in the previous 3 months • Patients with predominantly atopic dermatitis, in which the hands are also involved. (Patients with controlled atopic dermatitis, in which the hands are mainly affected, are eligible for inclusion.) • Psoriasis of the hands • Active bacterial, fungal, or viral infection of the hands • Pregnant/lactating or planning to become pregnant during the study period • Treatment with systemic medication or UV radiation within the previous 4 weeks. For systemic prednisolone; patients with treatment within the previous 2 weeks will be excluded • Mentally incompetent • Immunocompromised status • Uncontrolled arterial hypertension (minimally 3 measurements). Systolic pressure > 160 mmHg or diastolic pressure > 95 mmHg, despite starting anti-hypertensive medication (first choice amlodipine 5 mg/day) (17) • Known or suspected allergy to ingredients in the study medications • Inclusion in a study of an investigational drug within 60 days prior to start of treatment • Current malignancy (other than successfully treated non-metastatic cutaneous squamous cell or basal cell carcinoma and⁄or localized carcinoma in situ of the cervix) • Current active pancreatitis • Evidence of alcohol abuse or drug addiction • Malabsorption • Currently active gout • Recurring convulsions / epilepsy • Living vaccine (including bacillus Calmette-Guérin (BCG), varicella, measles, mumps, rubella, yellow fever, oral polio and oral typhoid) in the last 2 weeks or the planned application of such a vaccine during the study period • Chronic or recurrent infectious diseases • Contact sensitizations with clinical relevance to the hands, in which exposure to allergens is not avoided.Hypervitaminosis A due to the use of vitamin A supplements containing >2000 IU • Use of drugs with potential to change the effective dosis of study drugs within the previous 2 weeks
- Laboratory exclusion criteria post randomization • Alanine aminotransferase (ALAT) and ⁄or aspartate aminotransferase (ASAT) values > 200% of the upper limit of normal • Impaired renal function as indicated by a clinically relevant abnormal creatinine value (to be determined by investigator or treating physician) • Anemia as indicated by a clinically relevant lowered hemoglobin value (to be determined by investigator or treating physician)
- Alitretinoin specific • Triglycerides > 200% of the upper limit of normal, • Cholesterol or low density lipoprotein (LDL) cholesterol values > 200% of the upper limit of normal • Uncontrolled hypothyroidism (to be determined by investigator or treating physician)
- Cyclosporine specific: • Impaired renal function as indicated by a clinically relevant abnormal creatinine value (to be determined by investigator or treating physician) • Uremia • Hyperkalemia • Hyperuricemia in patients with a medical history of gout
The study team makes the final eligibility decision.
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18-64 years, 65+ years. The study team makes the final eligibility decision.
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BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from EU CTIS; the study team decides eligibility.