12-week Study of NFX-179 Gel in Subjects With Epidermal Nevi

Albert Chiou

Status and phase

Withdrawn

Phase 2

Conditions

Epidermal Nevi

Nevus Sebaceus

Treatments

Drug: NFX-179 Gel 1.50%

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT05195762

60276

Details and patient eligibility

About

This study of NFX-179 is an open-label study, evaluating safety, tolerability, pharmacodynamic activity, and the clinical effect in subjects with Epidermal Nevus(ENS). NFX-179 is formulated as a gel for topical administration. NFX-179 has been shown in animal studies and in human extracts to suppress p-ERK with systemic absorption of NFX-179 following topical application to be extremely low, based on serum values observed in animal studies.

Primary objectives:

To determine the pharmacodynamic activity of NFX-179 Gel as defined by suppression of phospho-ERK (p-ERK) levels in Target EN in treatment group after 12 weeks of once-daily (QD) application
To determine the safety and tolerability of treatment with NFX-179 Gel 1.50% applied QD for 12 weeks.

Secondary objectives:

-Clinical effect of NFX-179 Gel 1.5% defined as the percent change in EN volume after 12 weeks of QD application

Full description

This is a 12-week clinical study to determine safety, tolerability, and clinical effect of NFX-179 Gel 1.50% Gel in subjects with EN.

At Visit 1 (Screening), the Investigator will select 1 Target EN lesion for treatment that meet the inclusion criteria. A biopsy tissue sample of the Target EN will be taken for histological confirmation of an EN diagnosis if required, to assess p-ERK levels and for genetic testing.

Subjects will be seen at Visit 2 for management of the Visit 1 biopsy wounds.

At Visit 3 (Baseline) eligible subjects will be provided study medication and start the 12-week, QD treatment period. Target EN assessments will be collected.

Subjects will be seen for treatment period visits, Visits 4-7, when Target EN assessments will be collected.

At Visit 8, subjects will be seen for the final treatment period visit. Target EN assessments, a biopsy sample for genetic testing and p-ERK levels will be. Subjects will start a 4-week no-treatment follow-up period.

Subjects will be seen at Visit 9, for management of the Visit 8 biopsy wound.

At Visit 10 (end of study), subjects will be seen for the final study visit and will be discharged from the study.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria

In order to be eligible to participate in this study, all of the following criteria must be met:

Subject is at least 18 years of age
Subject must provide written informed consent prior to any study procedures
Subject has a Target Epidermal Nevi for treatment that:
- Is a documented, biopsy proven, keratinocytic epidermal nevi (KEN) or nevus sebaceous (NS) or has a 3mm punch biopsy taken for histologic examination to determine KEN or NS status
- Is a discrete lesion surrounded with at least 5mm of non-involved skin
- Is not irritated
- Does not have an active cutaneous infection
- Has a Length ≥15mm
- Has a surface area ≤100cm2
- Has an Investigator's Lesion Assessment grade ≥2
- Is located at an anatomical site that the subject can reach to apply the study medication
- Has never been surgically treated
Subject is willing to have hair in the area surrounding the Target EN shaved, if necessary, to obtain photographs
Subject is willing to minimize exposure of the Target EN to natural or artificial ultraviolet radiation
Subject is willing to abstain from application of non-study topical prescription and over the counter medications to the Target EN during the study
Subject is willing to forego treatment of the Target EN, except protocol specified therapy, during the study
Female subjects who are women of childbearing potential must have a negative urine pregnancy test result and be willing to use a protocol approved, contraceptive method for the duration of the study.
Subject is willing and able to follow all study instructions and to attend all study visits.

No waivers to the inclusion criteria are permitted.

Exclusion Criteria A potential subject who meets any of the following criteria will be excluded from participation in this study:

Subject has applied any of the following topical products in the previous 30 days on or in proximity to the Target EN that, in the investigator's opinion, impairs evaluation of the Target EN or which exposes the subject to an unacceptable risk by study participation:
- Topical glucocorticoid steroids
- Topical retinoids (e.g., tazarotene, tretinoin, adapalene)
- > 5% of an alpha-hydroxy acid (e.g., glycolic acid, lactic acid)
- Fluorouracil
- Imiquimod
The Target EN has ever been treated with a topical MEK inhibitor or a topical BRAF inhibitor
The Subject has used any of the following systemic medications in the noted time period:
- Systemic retinoids (e.g., etretinate, isotretinoin) in the previous 90 days
- Systemic MEK inhibitors in the previous 180 days
- Systemic BRAF inhibitors in the previous 180 days
Subject has a history of hypersensitivity to any of the ingredients in the study medications
Subject has any know intercurrent illness or physical condition that would, in the investigator's opinion, impair evaluation of the Target EN or which exposes the subject to an unacceptable risk by study participation
Subject has, in the Investigator's opinion, a clinically relevant history of liver disease, including viral hepatitis, current alcohol abuse, or cirrhosis
Subject has a history of metastatic disease, or active cancer (excluding non-melanoma skin cancer, Stage I cervical cancer, ductal carcinoma in situ of the breast, or Stage 0 chronic lymphocytic lymphoma) within the previous 5 years
Subject has any condition (e.g., other skin conditions or diseases, metabolic dysfunction, physical examination findings, clinical laboratory findings) or situation (e.g., vacation, scheduled surgery) that would, in the Investigator's opinion, impair evaluation of the Target EN or which exposes the subject to an unacceptable risk by study participation
Subject has participated in an investigational drug trial in which administration of an investigational study medication occurred within the previous 30 days No waivers to the exclusion criteria are permitted.