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Long-term Study of Ciclosporin for Atopic Dermatitis

Long-term Study of Ciclosporin for Atopic Dermatitis

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00232063
Enrollment
Unknown
Registered
2005-10-04
Start date
2004-05-31
Completion date
Unknown
Last updated
2011-11-02

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

Conditions

Severe Atopic Dermatitis

Keywords

Atopic Dermatitis, Ciclosporin,

Brief summary

In patients with severe adult atopic dermatitis, the safety and efficacy of OL27-400MEPC will be assessed by repeating oral administration at a dose of 3 mg/kg/day (2-5 mg/kg/day) in 2 divided doses daily for 8-12 weeks and recovery until 52 weeks after starting treatment

Interventions

DRUGciclosporin

Sponsors

Novartis Pharmaceuticals
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 64 Years

Inclusion criteria

* \- Appropriate the definition/diagnosis criteria of atopic dermatitis of the Japanese Dermatological Association * Patients with severest atopic dermatitis \[according to the Guidelines for Treatment of Atopic Dermatitis 2002, the severity of atopic dermatitis will be classified as severest when an eruption associated with severe inflammation (a lesion associated with erythema, papule, erosion, infiltration, lichenification, etc.) is noted on at least 30% of body surface on the day of subject enrollment\].

Exclusion criteria

* Patients who received oral preparations, injections, inhaled preparations and suppositories of steroids or immunosuppressants other than tacrolimus hydrate ointments within 14 days of subject enrollment * Patients who might receive the oral/injection drugs which are known to enhance nephrotoxicity, increase serum potassium levels, HMG-CoA reductase inhibitors or theophylline during the treatment period. * Patients who received or are receiving an ultraviolet therapy (PUVA therapy, etc.) * Patients with hypertension, active infectional disease, gout etc. Other protocol-defined

Outcome results

None listed

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