Study to Evaluate the Efficacy and Safety of 0.1% and 0.03% Tacrolimus Ointment Administered in Adults With Moderate to Severe Atopic Dermatitis

Dermatitis, Atopic Clinical Trial

Official title:

A Long-term, Non-comparative, Multi-centre Study to Evaluate the Efficacy and Safety of 0.1% and 0.03% Tacrolimus (FK506) Ointment Administered in Adults With Moderate to Severe Atopic Dermatitis FG-506-06-IT-01

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00691145
• Other study ID #: FG-506-06-IT-01
• Status: Completed
• Phase: Phase 3
• First received: June 3, 2008
• Last updated: August 28, 2014
• Start date: October 2002
• Est. completion date: February 2005

Study information

• Verified date: August 2014
• Source: Astellas Pharma Inc
• Contact: n/a
• Is FDA regulated: No
• Health authority: Italy: Ethics Committee
• Study type: Interventional

Clinical Trial Summary

The objective of this study is to assess the efficacy and safety of 0.1% and 0.03% Tacrolimus ointment for 12 months in adults with moderate to severe atopic dermatitis.

Description:

The main phase is 6 months duration, but the follow up phase up to 12 months will allow the collection of efficacy and safety data in a period which will include all seasons in each patient, to account for seasonal variability which strongly affect atopic dermatitis course.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 350
• Est. completion date: February 2005
• Est. primary completion date: February 2005
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patient may be male or female of any ethnic group

• Patient without restricted legal competence, and suffers from moderate to severe atopic dermatitis (Rajka/Langeland score of at least 4.5)

• Patient known to be responsive to topical steroids

• Patient is capable of understanding the purposes and risks of the trial and has given written Informed Consent

• Female patients of childbearing potential must agree to maintain adequate birth control practice during the trial period and during the first four weeks after the end of the study

• Patient meets the following criteria:

• Topical corticosteroids

• Systemic corticosteroids (for the treatment of AD only)

• Systemic non-steroidal immunosuppressants (e.g. cyclosporine, methotrexate)

• Other investigational drugs

• Light Treatments (UVA, UVB)

• Patient has not taken and agrees not to take for the complete study period any medication or therapy prohibited by the protocol

Exclusion Criteria:

• Patient has a genetic epidermal barrier defect such as Netherton's syndrome or generalised erythroderma

• Patient is pregnant or breast-feeding

• Patient has a skin infection on the affected (and to be treated) area

• Patient has a known hypersensitivity to macrolides in general, to tacrolimus or any excipient of the ointment

• Patient is simultaneously participating in any other drug trial or less than 28 days have passed between the end of the previous trial and this one

• Any form of substance abuse (including drug or alcohol abuse),psychiatric disorder or condition which, in the opinion of the investigator, may invalidate the communication with the investigator

• Patient is known to be HIV positive

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Dermatitis
• Dermatitis, Atopic
• Eczema

Intervention

Drug:
• tacrolimus ointment
transdermal

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Astellas Pharma Inc

Country where clinical trial is conducted

Italy, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The rate of patients with at least 50% (i.e. at least moderate) improvement according to the physician's global evaluation of clinical response at month 6/end of study (if before month 6) visit		1 year	No
Secondary	The rate of patients with at least 50%(i.e. at least moderate) improvement according to the physician's global evaluation of clinical response at month 12/end of study (if after month 6) visit		1 year	No
Secondary	The rate of patients with at least 60% improvement in the Score In Atopic Dermatitis (SCORAD) at month 6/end of study visit (if before month 6) and at month 12/end of study (if after month 6) visit, each compared to baseline (day 1)		1 year	No
Secondary	The incidence of adverse events during the study, including all clinically significant laboratory values		1 year	No

External Links

•   Link to Results on JAPIC - enter 140568 in the JapicCTI-RNo. field