A Phase 1 interventional study of RVT-501 0.5% topical ointment in Atopic Dermatitis, sponsored by Dermavant Sciences GmbH. Status unknown at 12 sites in United States. Open to participants aged 2 Years to 11 Years. Per ClinicalTrials.gov, last updated 2018-05-11.
Sponsored by Dermavant Sciences GmbH · Phase 1, Interventional, and Treatment
This is a multicenter, open-label Phase 1b study in pediatric patients age 2-11 years old with extensive atopic dermatitis.
The purpose of this multicenter, open-label study is to evaluate the safety, tolerability, and pharmacokinetics of RVT-501 0.5% topical ointment administered twice daily (BID) for 4 weeks in pediatric patients age 2-11 years of age with extensive atopic dermatitis. The efficacy of RVT-501 will also be evaluated as a secondary objective in these patients. The study will consist of three phases: Screening (up to 30 days), Treatment Phase (28 days), and Follow-up (7-10 days).
Females of childbearing potential and male patients, who are engaging in sexual activity that could lead to pregnancy, must use the following adequate birth control methods while on study and for 2 weeks after stopping study drug. Acceptable contraception methods are:
Male condom, AND partner use of one of the contraceptive options below:
These allowed methods of contraception are only effective when used consistently, correctly and in accordance with the product label. The Investigator is responsible for ensuring that patients understand how to properly use these methods of contraception.
Nonchildbearing potential is defined as premenarchal or premenopausal females with a documented bilateral tubal ligation, bilateral oophorectomy (removal of the ovaries) or hysterectomy; or hysteroscopic sterilization. Documented verbal history from the patient is acceptable.
Patients who are abstinent are eligible, but they must use one of the birth control methods listed above if they start engaging in sexual activity that could lead to pregnancy during the study.
Female patients of childbearing potential must have a negative pregnancy test at screening and Baseline (Day 0).
Exclusion Criteria:
Use of any prohibited medication. Prohibited concomitant medications, therapy, etc. during the defined period are as listed in the bullets below. If a patient requires any of these medications throughout the study period, he/she may be excluded from or discontinued from the study, at the discretion of the Investigator and medical monitor.
From 6 months prior to the first application of study drugs to the completion of the Follow-up visit or discontinuation:
From 28 days prior to the first application of study drug until the completion of the Follow-up visit or discontinuation:
Follow-up visit or discontinuation:
Topical corticosteroids that were classified as low, medium, or high potency (e.g., fluocinonide, triamcinolone acetonide, desonide, hydrocortisone). Eye drops and nasal preparations are allowed.
NOTE: The following antihistamines are allowed:
Open-label treatment arm - patients will receive RVT-501 0.5% twice daily (BID) for 4 weeks.
Drug: RVT-501 0.5% topical ointment
RVT-501 0.5% topical ointment twice daily (BID) for 4 weeks.
Frequency and severity of adverse events (local and systemic)
Adverse events will be coded using the most current release of MedDRA® (Medical Dictionary for Regulatory Activities). The number and proportion of subjects with adverse events will be summarized by treatment, system organ class, and preferred term for all adverse events, all adverse events considered by the investigator to be related to study drug, all serious adverse events, and all adverse events leading to study drug discontinuation
Time frame: 28 days
Laboratory values
Selected laboratory data will be summarized by the observed data and by the change from baseline (as appropriate) across time. Incidence of treatment emergent laboratory values that are considered clinically significantly abnormal will be summarized by treatment group.
Time frame: 28 days
Vital signs
Vital signs will be measured in supine or semi-supine position after a 5 minute rest and will include systolic and diastolic blood pressure and pulse rate. Vital sign data will be listed by subject and summarized by treatment.
Time frame: 28 days
Plasma concentrations of RVT-501
PK samples will be collected at week 1 pre-dose, 2-4 hours post-dose, and 6-8 hours post dose for all subjects. At week PK samples will be collected pre-dose. RVT-501 will be measured in plasma by validated assay in all subjects to confirm exposure. These plasma concentrations will be listed by metabolite, subject, treatment, and time; and will be summarized by analyte and time. If data permit, RVT-501 and M11 concentrations will be summarized descriptively at each collection time point.
Time frame: 28 days
Plasma concentrations of M11 metabolite
PK samples will be collected at week 1 pre-dose, 2-4 hours post-dose, and 6-8 hours post dose for all subjects. At week 4 PK samples will be collected pre-dose. The M11 metabolite will be measured in plasma by validated assay in all subjects to confirm exposure. These plasma concentrations will be listed by metabolite, subject, treatment, and time; and will be summarized by metabolite, treatment and time. If data permit, RVT-501 and M11 concentrations will be summarized descriptively at each collection time point.
Time frame: 28 days
Efficacy - Investigators Global Assessment (IGA)
Efficacy will be evaluated as the change from Baseline in IGA score.
Time frame: 28 days
Efficacy - 2-point improvement in IGA
Efficacy will be evaluated by the proportion of patients who achieve an IGA of 0 or 1 with at least a 2-point improvement from Basline
Time frame: 28 days
Efficacy - IGA of 0 or 1 at study end
Efficacy will be evaluated by the proportion of patients who achieve an IGA of 0 or 1 at Week 4.
Time frame: 28 days
Efficacy - Eczema Area and Severity Index (EASI) score
Efficacy will be evaluated as the change from Baseline in EASI score.
Time frame: 28 days
Efficacy - EASI-50
Efficacy will be evaluated by the proportion of patients who achieve at least a 50% reduction from Baseline EASI (EASI-50) at Week 4.
Time frame: 28 days
Efficacy - Peak Pruritus Numeric Rating Scale (NRS)
Efficacy will be evaluated as the change from Baseline in Peak Pruritus as measured with the NRS at Week 4.
Time frame: 28 days
Efficacy - Body Surface Area (BSA)
Efficacy will be evaluated as the change from Baseline in BSA affected by disease at Week 4.
Time frame: 28 days
Efficacy - Patient/caregiver reported itch severity (local)
The patient or their caregiver will assess itch severity at the application site and efficacy will be determined as a change from Baseline.
Time frame: 28 days
Efficacy - Patient/caregiver reported itch severity (global)
The patient or their caregiver will assess global itch severity and efficacy will be determined as change from Baseline.
Time frame: 28 days
Plan to share: Undecided
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Dermavant Sciences GmbH