SHP-141C in Plaque Type Psoriasis
Information source: TetraLogic Pharmaceuticals
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Plaque Type Psoriasis
Intervention: SHP-141C (Drug); Placebo to SHP-141C (Drug); Betamethasone Valerate (Drug); Calcipotriol (Drug)
Phase: Phase 1
Status: Completed
Sponsored by: TetraLogic Pharmaceuticals Official(s) and/or principal investigator(s): Peter Foley, Principal Investigator, Affiliation: The Alfred
Summary
The purpose of this study is to assess the safety, tolerability and clinical activity of the
SHP-141C topical cream formulations in patients with plaque type psoriasis.
Clinical Details
Official title: A Double-Blind, Within-Subject Randomised, Placebo-Controlled, Proof of Concept, Comparison Study of SHP-141C Topical Cream in Psoriasis, Using the Microplaque Assay.
Study design: Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Primary outcome: Change from baseline in Local Plaque Severity Index (LPSI)
Secondary outcome: The number of patients with adverse events
Detailed description:
Psoriasis is a chronic, relapsing immunoinflammatory disorder. Chronic plaque psoriasis is
the most common (85% - 90%) type. Cutaneous features of individual plaques include circular
with centrifugal expansion, induration with sharp demarcation from surrounding skin,
erythema and hyperkeratosis. Psoriasis has a negative impact on physical and mental aspects
of life that is similar to other major chronic conditions. The modalities of psoriasis
treatments can be divided into four main categories: topical, phototherapy, systemic drug
therapies and systemic biological treatments. The currently available treatments for
psoriasis result in either disease suppression or disease remission. There are many treatment
options for the management of psoriasis using topical modalities; however all are lacking
with respect to patient satisfaction and durability of treatment. Most current topical
treatments, and many treatments in development, are based on modifications of a steroid
structure or on Vitamin D. Recent research has identified a broad role for histone
deacetylase (HDAC) proteins in numerous signaling pathways critical to cancer cell survival,
such as epigenetic inheritance, gene regulation, mitosis,signal transduction and
importantly, inflammation. Theoretically modulation of HDAC could lead to clinical benefit
in inflammatory diseases.
Eligibility
Minimum age: 18 Years.
Maximum age: 70 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
1. Mild to moderate chronic plaque-type psoriasis.
2. psoriasis of at least one year.
3. Stable disease for at least two weeks prior to the commencement of study treatment.
4. One nominated target lesions must have areas of at least 86 x 57 mm2.
5. BMI of less than 35 kg/m2. -
Exclusion Criteria:
1. Dermatological Conditions
- Subjects with erythrodermic, guttate, palmar, plantar or generalised pustular
forms of psoriasis.
- Subjects with scalp, palmar or plantar psoriasis only.
- Subjects with any skin condition other than psoriasis, in particular eczema,
cutaneous infections, significant sun damage or an inherited skin disorder
(other than psoriasis).
2. Concurrent Medical Conditions
- History of clinically significant intercurrent disease of any type (other than
psoriasis).
- A history of moderate or severe asthma during the last 10 years.
- Major chronic inflammatory disease .
- Congenital immunodeficiency or cancer prone syndrome.
- History of abnormal bleeding tendencies or thrombophlebitis, or a history of
Hepatitis B, Hepatitis C or HIV infection.
- History of malignancy (other than adequately treated skin carcinoma or
carcinoma-in-situ of the cervix).
3. Laboratory Status
- Any evidence of organ dysfunction, which is confirmed on re-examination to be
clinically significant (i. e. in the opinion of the Medical Officer would
jeopardise the safety of the subject or impact on the validity of the study
results),
- A creatinine clearance of less than 75 mL/min.
- Liver function test > 1. 5 x upper limit of normal other than an isolated
bilirubin.
- Hepatitis B surface antigen, Hepatitis C antibody, HIV antibodies.
4. Treatment with any of the following within 4 weeks prior to the commencement of study
treatment and for the duration of the study:
- Systemic retinoids.
- Immunosuppressant agents (e. g. methotrexate, cyclosporine, azathioprine,
thioguanine prednisone, prednisolone, hydroxyurea or mycophenolate mofetil).
- Phototherapy or photochemotherapy.
- High potency topical corticosteroids.
- "Alternative medicine" treatments for psoriasis.
- Prolonged sun exposure or tanning bed use, which may in the opinion of the
Investigator, modify disease activity.
5. Topical treatment of the 2 target lesions with any of the following within 2 weeks
prior to commencement of study treatment and for the duration of the study
- Moderate potency topical corticosteroids.
- Vitamin D analogues and topical retinoids.
- Keratolytics, coal tar and dithranol.
6. Concurrent Medications Subjects have received or anticipate receiving a new medicine
(prescription, over-the-counter or herbal), given systemically or topically, within
14 days prior to the start of dosing. Subjects may be enrolled if stable on existing
therapy (having been on it for at least 60 days) as determined by the Principal
Investigator.
7. Hypersensitivity History of allergy and/or hypersensitivity to any of the stated
ingredients of the formulations or other topical agents. A known hypersensitivity to
lignocaine, or all surgical dressings that may be used in the study procedures.
8. Females who are lactating, pregnant or planning to become pregnant.
9. Drug and Alcohol Abuse History of, or current evidence of, abuse of alcohol or any
drug substance, licit or illicit, or positive urine drug and alcohol screen for drugs
of abuse and alcohol.
10. Psychiatric Disorder History of any psychiatric illness which may impair the ability
to provide written informed consent
11. Participation in a research study within 30 days of the start of dosing.
Locations and Contacts
Nucleus Network Limited, Melbourne, Victoria 3004, Australia
Additional Information
Starting date: September 2012
Last updated: July 10, 2014
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