Study to Test the Effectiveness of a New Treatment for Scalp Psoriasis

Psoriasis Clinical Trial

Official title:

Phase II Study of a Non-Steroidal Novel Treatment for Scalp Psoriasis

Clinical Trial Details — Status: Suspended

Administrative data

• NCT number: NCT01368887
• Other study ID #: DermiPsor 2008-103
• Status: Suspended
• Phase: Phase 2
• First received: June 6, 2011
• Last updated: June 7, 2011
• Start date: April 2013
• Est. completion date: April 2014

Study information

• Verified date: June 2011
• Source: DermiPsor, Ltd.
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to test the effectiveness of DermiPsor's DPS-102 (test product) in patients with scalp Psoroasis. The study is also intended to assess the safety of the product.

Description:

Psoriasis is a non-contagious skin disorder affecting up to 2% of the world population. It is estimated that 26 million people in the U.S. and Europe suffer from psoriasis. Forty percent (40%) of these suffer from psoriasis of the scalp. Currently, there are three primary modalities for the treatment of psoriasis: topical, phototherapy and systemic treatments. While existing treatments provide varying degrees of relief for this illness, they do not provide a long-term cure. Additionally, there is evidence that some of these existing treatments may cause significant side effect. The purpose of this study is to demonstrate that DermiPsor's DPS-102 (test product) is statistically more effective for the treatment of psoriasis current topical treatment options. It is also intended to assess the safety of DPS-102.

Recruitment information / eligibility

• Status: Suspended
• Enrollment: 160
• Est. completion date: April 2014
• Est. primary completion date: November 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Male or female of age 18 or older

• Patient with a personal history of scalp psoriasis

• Patient with treatable lesions

• Patient with a TSS score equal or lower than 9.

• Patient with a PGA score equal or lower than 5.

• Patient with a negative urine pregnancy test at inclusion for women of childbearing potential and using an efficient contraceptive (oral contraceptives, IUD, or tubal ligation)

• Patient agreeing to participate to the study and to sign a written informed consent and comply with study requirements.

Exclusion Criteria:

• Patient treated with topical scalp treatment for scalp psoriasis within two weeks prior to the inclusion in the study (corticoids, retinoids, vitamin D derivatives),

• Patient treated with systemic treatment for psoriasis (biologics, methotrexate, cyclosporine, retinoids) within one month prior to the inclusion in the study

• Patient taking systemic niacin or multivitamins within past two weeks

• Patient who start or modify a treatment with beta-blockers within one month prior to the inclusion in the study

• Patient with PEG (Poly Ethylene Glycol) allergy

• Pregnant or breast feeding female or female who do not use contraception,

• Patient with an history of hypersensitivity to Dovonex/Daivonex

• Patient who has participated in a clinical trial within three month prior inclusion,

• Patients on Carbamazepine and Primidione (the clearance of Primidione and Carbamazepine may be reduced with the concomitant use of Nicotinamide)

• Patient who is under guardianship, or unable to understand the information (for linguistic or mental reason), or unwilling to give her/his informed consent to participate in the study

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Psoriasis

Intervention

Drug:
• DPS-102
The patient will apply the treatment twice daily in the morning and at bedtime on the involved area only. The scheduled treatment duration is 12 weeks. Patient to begin treatment on the night of Visit 1.

Other:
• Vehicle / Placebo
The patient will apply the vehicle twice daily in the morning and at bedtime on the involved area only. The scheduled treatment duration is 12 weeks. Patient to begin treatment on the night of Visit 1.

Drug:
• Calcipotriol Monotherapy
The patient will apply the treatment twice daily in the morning and at bedtime on the involved area only. The scheduled treatment duration is 12 weeks. Patient to begin treatment on the night of Visit 1.
• Nicotinamide Monotherapy
The patient will apply the treatment twice daily in the morning and at bedtime on the involved area only. The scheduled treatment duration is 12 weeks. Patient to begin treatment on the night of Visit 1.

Locations

Country	Name	City	State
United States	Boston VA Hospital	Boston	Massachusetts
United States	Brockton VA Hospital	Brockton	Massachusetts

Sponsors (1)

Lead Sponsor	Collaborator
DermiPsor, Ltd.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The Physician's Global Assessment ("PGA") criteria. The PGA involves a 7 point scale (clear, minimal, mild, moderate, severe and very severe) and grading conducted at 0, 2, 4, 8 and 12 weeks.	The number of participants at each PGA scale level assessed at 0,2,4,8,and 12 weeks and a comparison of each individual's scale assessments over the 12 week period to assess any changes.	12 weeks	No
Secondary	Review of haematology and blood chemistry test results, and any adverse event reports received.	Number of participants who experience adverse events and type of adverse event in each case.	12 weeks	Yes