Non-steroid, Atopic Dermatitis Phase IIb 12-week Trial; Topical WBI-1001 Cream

Dermatitis, Atopic Clinical Trial

Official title:

A 12-week Efficacy Evaluation of WBI-1001 Cream in Patients With Atopic Dermatitis: A Multi-centered, Double-blinded Study (6-week Placebo-controlled Phase Followed by a 6-week Non-placebo Controlled Phase).

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01098734
• Other study ID #: WBI-1001-202 : # 133148
• Secondary ID: # 133148
• Status: Completed
• Phase: Phase 2
• First received: April 1, 2010
• Last updated: June 9, 2011
• Start date: November 2009
• Est. completion date: November 2010

Study information

• Verified date: June 2011
• Source: Welichem Biotech Inc.
• Contact: n/a
• Is FDA regulated: No
• Health authority: Canada: Health Canada
• Study type: Interventional

Clinical Trial Summary

Welichem Biotech has developed a small molecule drug candidate, WBI-1001, that selectively targets the pathogenic features of inflammatory skin diseases, including atopic dermatitis (a form of eczema).The purpose of this clinical trial is to further test the safety and efficacy of WBI-1001 as a topically applied cream over an extended period of 12 weeks on patients with mild to moderate atopic dermatitis.

Description:

A multi-centered, double-blinded Phase IIb study to evaluate the safety and efficacy of the non-steroid, anti-inflammatory WBI-1001 cream in the topical treatment of patients with mild to moderate atopic dermatitis, expressed as lesions up to 20% BSA. For the first 6 weeks patients will be randomized to one of three treatment groups simultaneously in a ratio of 1:1:1.

Group 1: vehicle cream (placebo), BID; Group 2: 0.5% WBI-1001 cream, BID; Group 3:1.0% WBI-1001 cream, BID. Patients randomized to treat all lesion areas.

After the first 6 weeks all patients will be treated, non-placebo controlled, with WBI-1001 cream. The Group 1 patients will enter a double-blinded phase for a further 6 weeks with half of them being treated BID with 0.5% and half with 1.0% WBI-1001 cream. Groups 2 and 3 will continue with their treatments unchanged for the remaining 6 weeks.

During the treatment period, patients will apply the cream (BID) from the kit that they have been provided, and they will visit the study centre at prescribed times for assessment of efficacy, safety and tolerability. After completion of the 12-week treatment period patients will have a 2-week follow-up visit.

Patients who withdraw from the study before Day 42 for reasons other than a treatment related AE will be replaced so that at least 40 patients per group will complete the placebo-controlled phase.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 148
• Est. completion date: November 2010
• Est. primary completion date: October 2010
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Clinical diagnosis of chronic atopic dermatitis (Hanifin's criteria) for greater than 6 months with a minimum of 5% and a maximum of 20% BSA.

• IGA scores of 2-4 at Day 0.

• WOCBP must have a negative serum beta-hCG pregnancy test before randomization, and they and their male partners must take pregnancy precautions for the duration of the study, as also must male patients.

• Willing to comply with Protocol and attend all visits.

• Provide written informed consent prior to entering study procedures.

• Patient has no latent or active tuberculosis infection according to medical history or current examination and tests.

Exclusion Criteria:

• Pregnancy or lactation.

• Spontaneously improving or rapidly deteriorating atopic dermatitis.

• Presence of atopic dermatitis on only hands and/or feet.

• Any skin disease other than atopic dermatitis that might interfere with clinical assessment or put patient at risk.

• Active allergic contact dermatitis or other non-atopic forms of atopic dermatitis.

• Other concommitant serious illness or medical condition, virus or renal insufficiency, or clinically significant abnormality that could put patient at risk during the study.

• History of neurological/psychiatric disorders including psychotic disorders, dementia or any other reason that would interfere with the patient's participation.

• Systemic immunomodulatory therapies for other conditions within 4 weeks prior to the baseline visit.

• Any phototherapy, photochemotherapy or systemic atopic dermatitis therapy within 2 weeks of the baseline visit.

• Prolonged exposure to natural or artificial sources of UV within 4 weeks prior to baseline visit or intention to have such exposure during the study.

• Topical atopic dermatitis therapies (including corticosteroids and calcineurins) in the areas to be treated within 2 weeks prior to baseline.

• Alcohol abuse in the last 2 years.

• Allergic history to any of the non-medical ingredients of the study cream.

• Treatment with an investigational drug within one month of Day 0 or current participation in another clinical trial.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Dermatitis
• Dermatitis, Atopic
• Eczema

Intervention

Drug:
• WBI-1001
A 12-week study to assess the efficacy, safety and tolerability of topically applied WBI-1001 creams. First 6 weeks will be double-blinded, placebo-controlled and the following 6 weeks will be double-blinded, non-placebo- controlled. After 6 weeks patients in Groups 2 and 3 will continue double-blinded treatment for a further 6 weeks, but patients in Group 1 will enter a 6-week double-blinded phase with one of the two active creams (half treated with 0.5% and half with 1.0% WBI-1001 cream). All patients treated twice daily (BID).

Locations

Country	Name	City	State
Canada	Innovaderm Research Inc.	Montreal	Quebec
Canada	Centre de Recherche Dermatologique du Quebec	Quebec City	Quebec
Canada	Guilford Dermatology Associates	Surrey	British Columbia
Canada	Department of Dermatology and Skin Sciences, UBC	Vancouver	British Columbia
Canada	Windsor Clinical Research Inc.	Windsor	Ontario

Sponsors (1)

Lead Sponsor	Collaborator
Welichem Biotech Inc.

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Investigator's Global Assessment (IGA) score	To evaluate the efficacy of the 0.5% and 1.0% WBI-1001 creams in comparison with the vehicle placebo.	The change from baseline to 6 weeks.	No
Secondary	Eczema Area and Severity Index (EASI) score	Comparison over time with the placebo.	The change from baseline to 6 weeks.	No
Secondary	Scoring Atopic Dermatitis (SCORAD) Index.	Comparison over time with the placebo.	Change from baseline to 6 weeks.	No
Secondary	Clinical laboratory tests (haematology, urine) and vital signs.		From baseline through 12 weeks+2 weeks follow-up	Yes
Secondary	Adverse events		From baseline through 12 weeks+2 weeks follow-up	Yes
Secondary	BSA and pruritus.	Comparison over time with placebo.	From baseline through 6 weeks.	No
Secondary	Longterm change in IGA score of WBI-1001 cream groups.	Long term comparison, non-placebo, of the 0.5% and 1.0% cream treated groups of patients	Change from baseline through 12 weeks	No
Secondary	Statistically significant improvement in the rate of "Treatment Success" with 0.5% and 1.0% WBI-1001 creams compared with placebo.	"Treatment Success" is defined as a patient who (1) achieves "clear" (IGA=0) or "almost clear" (IGA=1) on a five-point IGA scale or (2) has a minimum of 2-point improvement in IGA score over the baseline.	First 6 weeks	No