NFX-179 Topical Gel Treatment in Adults With Neurofibromatosis 1 (NF1) and Cutaneous Neurofibromas (cNF)

Neurofibromatosis 1 Clinical Trial

Official title:

A Randomized, Double-Blind, Vehicle-Controlled, Parallel Group Phase 2a Study to Determine Safety, Tolerability, Pharmacokinetics, and Pharmacodynamic Activity of NFX-179 Gel in Subjects With Cutaneous Neurofibromas

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04435665
• Other study ID #: NFX-179-NF1-201
• Status: Completed
• Phase: Phase 2
• Start date: August 21, 2020
• Est. completion date: April 14, 2021

Study information

• Verified date: July 2022
• Source: NFlection Therapeutics, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will enroll and treat subjects with cutaneous neurofibromas with NFX-179, a topical study drug. Eligible subjects will receive treatment for 28 days and be observed by a study doctor for approximately 56 days. Subjects will be randomly assigned to 1 of 4 treatment groups. 3 of the treatment groups will receive a specific dose NFX-179, and 1 group will receive placebo. The subject, study doctor, and NFlection Therapeutics will not know what treatment group each subject is assigned. Study participation requires at least 7 clinic visits, blood, urine, and tissue collection, images of the treated cutaneous neurofibromas, electrocardiograms, and information regarding the subject's medical and disease history.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 48
• Est. completion date: April 14, 2021
• Est. primary completion date: April 8, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Subject is at least 18 years of age

2. Subject must provide written informed consent prior to any study procedures

3. Subject must have a clinical diagnosis of NF1

4. Subject has 6 Study cNF Tumors (5 Target cNF Tumors [1 on the face; 4 on the anterior trunk or upper extremities] that will be treated with the assigned study medication;1 Untreated cNF Tumor on the anterior trunk or upper extremities) that each meet the

following criteria:

• Has, in the investigator's opinion, a clinically typical appearance
• Is dome shaped
• Is not pedunculated
• Is a discrete tumor
• Is not irritated
• Is not in an area subject to repeated trauma (e.g., area that is shaved, on the beltline, under a bra strap, etc.)
• Does not have an active cutaneous infection
• Has a diameter that is =5mm and =10mm
• Has a height of =2mm
• Is, when centered in the center of the provided template, the only cNF tumor visible
• Is not within 5mm of the orbital rim.

5. Subject is willing to have the 5 Target cNF Tumors and the 1 Untreated cNF Tumor excised at the end of the treatment period

6. Subject is willing to have hair in the area surrounding the Target cNF Tumors shaved, if necessary, to obtain photographs

7. Subject is willing to minimize exposure of each Target cNF to natural and artificial ultraviolet radiation

8. Subject is willing to forego treatment of the Target cNF Tumors, except protocol specified therapy, during the study

9. 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

10. Subject is willing and able to follow all study instructions and to attend all study visits.

Exclusion Criteria:

1. Subject has applied any of the following topical products in the previous 30 days on or in proximity to any Study cNF Tumor that, in the investigator's opinion, impairs evaluation of any the tumor or which exposes the subject to an unacceptable risk by

study participation:

• Corticosteroids
• Retinoids (e.g., tazarotene, tretinoin, adapalene)
• > 5% of an alpha-hydroxy acid (e.g., glycolic acid, lactic acid)
• Fluorouracil
• Imiquimod

2. Any Study cNF Tumor has ever been treated with an MEK inhibitor or a BRAF inhibitor

3. The subject has used any of the following systemic medications in the noted time

period:

• Retinoids (e.g., etretinate, isotretinoin) within the previous 90 days
• MEK inhibitors within the previous 180 days
• BRAF inhibitors within the previous 180 days

4. Subject has a history of hypersensitivity to any of the ingredients in the study medications

5. Subject has any known intercurrent illness or physical condition that would, in the investigator's opinion, impair evaluation of a Target cNF Tumor or which exposes the subject to an unacceptable risk by study participation

6. Subject has, in the investigator's opinion, clinically relevant history of liver disease, including viral hepatitis, current alcohol abuse, or cirrhosis

7. Subject has a history of metastatic disease, or active cancer (excluding nonmelanoma skin cancer, Stage I cervical cancer, ductal carcinoma in situ of the breast, or Stage 0 chronic lymphocytic lymphoma) within the previous 5 years

8. 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 a Target cNF Tumor or which exposes the subject to an unacceptable risk by study participation

9. Subject has participated in an investigational drug trial in which administration of an investigational study medication occurred within the previous 30 days

Related Conditions & MeSH terms

• Cutaneous Neurofibroma
• Neurofibroma
• Neurofibromatoses
• Neurofibromatosis 1

Intervention

Drug:
• NFX-179 Gel
gel for topical administration
• Vehicle Gel
vehicle gel for topical administration

Locations

Country	Name	City	State
United States	DermResearch	Austin	Texas
United States	University of Texas Southwestern Medical Center	Dallas	Texas
United States	Center for Dermatology Clinical Research, Inc.	Fremont	California
United States	The Education & Research Foundation, Inc.	Lynchburg	Virginia
United States	Minnesota Clinical Study Center	New Brighton	Minnesota
United States	Skin Search of Rochester, Inc.	Rochester	New York

Sponsors (1)

Lead Sponsor	Collaborator
NFlection Therapeutics, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Phospho-erk (p-ERK) Levels of Target cNF Tumors in NFX-179 Gel Group and Vehicle Gel Group After 28 Days of Once-daily (QD) Application	Pharmacodynamic activity (biochemical and physiologic effects of drugs) of NFX-179 Gel as defined by suppression of phospho-ERK (p-ERK) levels in Target cNF Tumors in each NFX-179 Gel group compared with the Vehicle Gel group after 28 days of once-daily (QD) application will be measured at Week 4	Baseline through Week 4
Primary	Safety and Tolerability of NFX-179 Gel Measured by Local Tolerability Assessment	Safety and tolerability will be measured via a local tolerability assessment. The investigator will assess erythema, edema, scabbing/crusting, vesiculation, and erosion. The subject will assess stinging, burning, and pruritus. All assessments are performed using a 4-point scale (0 none, 1 mild, 2 moderate, 3 severe).	Baseline through Week 4
Primary	Assessment of Adverse Events	Assessment of adverse events (AEs)	Baseline through Week 8
Secondary	Percent Change in cNF Tumor Volume (Cubic Millimeters)	Percent change in cNF tumor volume after 28 days of QD applications of NFX-179 gel based on tumor volume derived from ruler measurements.	Baseline through Week 4
Secondary	Systemic Exposure of NFX-179 Gel Measured by Plasma Concentration	Systemic exposure of NFX-179 will be measured during the 28 days of QD applications at select investigative sites. Pharmacokinetic samples will be drawn at the baseline visit and week 4 visit. 5 time point samples will be collected at the week 4 visit.	Baseline through Week 4
Secondary	Change in Physician Assessment of Tumor Severity Score	Effect of treatment with The Physician Tumor Assessment is the investigator's assessment of the average overall severity of each Target cNF tumor at a particular time point. The Physician Tumor Assessment is a 5-point measuring tumor severity (0 clear/none, 1 almost clear, 2 mild, 3 moderate, 4 severe). The assessment is performed at the Baseline visit and week 4 visit.	Baseline through Week 4
Secondary	Change in Subject Self-Assessment of Tumor Severity Score	The Subject Self-Assessment is the subject's assessment of the average overall severity of each Target cNF at a particular time point and is not a comparison with any other time point. The Subject Self-Assessment is a 5-point measuring tumor severity (0 clear/none, 1 almost clear, 2 mild, 3 moderate, 4 severe). The assessment is performed at the Baseline visit and week 4 visit.	Baseline through Week 4