A Study of the Safety and Efficacy of UHE-105 Shampoo in Subjects With Scalp Psoriasis

Completed · Phase 2 · Has a placebo group

Conditions studied: Scalp Psoriasis

In brief

This study is to compare the safety and efficacy of UHE-105 Shampoo with that of the vehicle (VEH) Shampoo in subjects with scalp psoriasis. Half of the subjects will receive the UHE-105 Shampoo, while the other half will receive the VEH Shampoo with no active drug.

Key facts

Study ID

NCT04243486

Run by

Therapeutics, Inc.

People needed

22

Starts

2020-01-02

Expected to finish

2020-06-15

Last updated by the study team

2020-07-09

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subject is a male or non-pregnant female 18 years of age or older.
• Subject has provided written informed consent.
• Females must be post-menopausal , surgically sterile or use an effective method of birth control. , Women of childbearing potential must have a negative urine pregnancy test at Visit 1/Baseline.
• Subject has a clinical diagnosis of stable moderate to severe scalp psoriasis affecting at least 10% of the scalp.
• Subject is willing and able to apply the test article(s) as directed, comply with study instructions, and commit to all follow-up visits for the duration of the study.
• Subject, in the investigator's opinion, is in good general health and free of any disease state or physical condition that might impair evaluation of scalp psoriasis or exposes the subject to an unacceptable risk by study participation.

You may not qualify if…

• Subject is pregnant, lactating, or is planning to become pregnant during the study.
• Subject has spontaneously improving or rapidly deteriorating scalp psoriasis.
• Subject has guttate, pustular, erythrodermic, or other non-plaque forms of scalp psoriasis.
• Subject has any physical condition which, in the investigator's opinion, could impair evaluation of scalp psoriasis, adrenal axis function (e.g., Addison's Disease, Cushing's Syndrome), or which exposes the subject to an unacceptable risk by study participation.
• Subject has scalp psoriasis that necessitates systemic or other concomitant topical therapies during the study.
• Subject has a history of psoriasis unresponsive to topical treatments.
• Subject has any hair on their scalp of a length that extends beyond the subject's chin.
• Subject has any open sores, lesions, cuts, or infections, etc. on the scalp or has had a scalp surgical procedure within the past 30 days.
• Subject is currently enrolled in an investigational drug or device study.
• Other protocol defined inclusion or exclusion criteria assessed by the study staff may apply.

Where it is running

• 01 — San Diego, California, United States
• 02 — High Point, North Carolina, United States

Full record on ClinicalTrials.gov

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