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A Study to Determine the Efficacy of Taclonex Topical Suspension as a Supplement to Non-biologic Systemic Therapy

Information source: University of Pittsburgh
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Psoriasis

Intervention: Taclonex Topical Suspension (Drug)

Phase: Phase 4

Status: Recruiting

Sponsored by: University of Pittsburgh

Official(s) and/or principal investigator(s):
Laura Ferris, MD, PhD, Principal Investigator, Affiliation: University of Pittsburgh

Summary

Oral therapies for psoriasis, including methotrexate and acitretin, are often less effective when used as monotherapy (without other oral medicines or creams) than are newer biologic injected drugs. However, these oral medications are also less expensive than biologic agents and may be safer for use in some patients. The purpose of this study is to determine if adding a topical psoriasis medicine, Taclonex topical suspension, will improve the severity of psoriasis in patients already on methotrexate or acitretin and to determine if adding this topical suspension will reduce the desire of such patients to switch to a biologic agent to treat their psoriasis.

Clinical Details

Official title: A Preliminary, Open Label, Single-arm Study to Determine the Efficacy of Taclonex Topical Suspension as a Supplement to Non-biologic Systemic Therapy

Study design: Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Primary outcome: Investigator Global Assessment

Secondary outcome:

Body surface area

safety

Patient satisfaction

Eligibility

Minimum age: 18 Years. Maximum age: N/A. Gender(s): Both.

Criteria:

Inclusion Criteria:

- Subjects age 18 years and older with stable plaque psoriasis of duration of at least

6 months.

- Subject must be currently using a stable dose, with stable disease severity, of a

single non-biologic systemic psoriasis medication (methotrexate or acitretin) for at least 2 months.

- Subject must be planning to continue current systemic agent, and standard of care

monitoring for that medication

- All labs required for methotrexate or acitretin will be done according to standard of

care.

- If a woman, before entry she must be: Postmenopausal, or practicing a highly

effective method of birth control

- Women of childbearing potential must have a negative urine pregnancy test prior to

randomization

- Subject must be able and willing to provide written informed consent to participate.

Exclusion Criteria:

- Non-plaque psoriasis (pustular, erythrodermic, or guttate).

- Use of excluded therapies: phototherapy use currently or in the 4 weeks prior to

baseline, use of more than 1 systemic therapy in the 2 months prior to baseline, use of topical steroid, tar preparation, or vitamin D analog in the 4 weeks prior to baseline.

- Subjects who are currently taking or have taken in the past 60 days, for any reason,

any medication that, in the opinion of the investigator, suppressed the immune response. This may include but is not limited to systemic steroids, azathioprine, cyclosporine, FK506, mycophenolate mofetil, mycophenolic acid, etanercept, adalimumab, infliximab, ustekinumab, cimzia, or any other biologic agent targeted to any cell or cytokine in the immune system.

- Subjects with any use at any time in the past of Taclonex topical suspension or

Taclonex ointment

- Subjects who are pregnant, nursing, or plan on becoming pregnant during the course of

the study.

- Presence of any unstable medical or psychiatric condition that, in the opinion of the

investigator, could impair subject compliance.

- Subject has any active infection within 30 days prior to baseline.

- Known or suspected disorders of calcium metabolism

- Known or suspected severe kidney or liver disease.

- Known or suspected hypersensitivity to component(s) of the investigational products.

Locations and Contacts

UPMC Department of Dermatology, Falk Clinic, Pittsburgh, Pennsylvania 15213, United States; Recruiting
Laura Ferris, MD,PhD, Phone: 412-647-9287, Email: dermtrials@upmc.edu
Laura K Ferris, MD, PhD, Principal Investigator
Erine Kupetsky, DO, Sub-Investigator
Additional Information

UPMC Dermatology Clinical Trials

Starting date: January 2013
Last updated: January 3, 2013

Page last updated: August 23, 2015

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