Efficacy and Safety of Sorilux in Maintenance Treatment of Moderate Type Plaque Psoriasis

Status unconfirmed · Phase 4

Conditions studied: Plaque Psoriasis

In brief

The study seeks to show whether there is additional benefit of using Lexette and Sorilux in the beginning of the treatment, and then maintenance treatment of Sorilux alone in moderate plaque type psoriasis patients.

Key facts

Study ID

NCT04571151

Run by

Skin Sciences, PLLC

People needed

30

Starts

2021-01-01

Expected to finish

2021-12-01

Last updated by the study team

2020-11-20

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Outpatient, male or female subjects of any race, 18 years of age or higher. Female subjects of childbearing potential must have a (-)UPT result at within 7 days of the first dose of study drug and practice a reliable method of contraception throughout the study;
• A female is considered of childbearing potential unless she is:
• postmenopausal > 5Y, without a uterus and/or both ovaries; or has been surgically sterile for > 6M.
• Reliable methods of contraception are:
• hormonal methods or IUD in use > 90d prior to study drug administration, barrier methods plus spermicide in use > 14d prior, or vasectomized partner.
• [Exception: Female subjects of CBP who are not sexually active are not required to practice a reliable method of contraception and may be enrolled at the Investigator's discretion provided they are counseled to remain sexually inactive for the duration of the study and understand the risks involved in getting pregnant during the study.]
• Subjects with moderate plaque type psoriasis.
• Physician Global Assessment (PGA) score of 3.
• Able to understand study requirements and sign Informed Consent/HIPAA forms.
• Target lesion must be at least 2cm in diameter

You may not qualify if…

• Female subjects who are pregnant, breast-feeding, or who are of childbearing potential and not practicing a reliable method of birth control, or male subjects planning a pregnancy with their spouse or partner while in the study.
• History of hypercalcemia or vitamin D toxicity or history of significant renal or hepatic disease
• Patients with guttate, erythrodermic, or pustular psoriasis
• Serious skin condition (other than psoriasis) or uncontrolled medical condition (in the opinion of the investigator).
• Skin conditions (e.g. eczema) that may interfere with evaluations of psoriasis.
• Known hypersensitivity to Lexette or Sorilux Foam or any of its components.
• Current drug or alcohol abuse (Investigator opinion).
• Subject unable to commit to all the assessments required by the protocol.
• Current enrollment in another clinical study and treatment with another experimental drug or approved therapy for experimental use within 30 days prior to the Screening Visit.

Where it is running

• Skin Sciences, PLLC — Louisville, Kentucky, United States

Full record on ClinicalTrials.gov

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