An 18-week Study to Evaluate a Test Product With a Marketed Prescription Product

Part of paid clinical trials in Teaneck, New Jersey.

Sponsor
Good Molecules, LLC
Study ID
NCT07136766
Phase
PHASE3
Status
Enrolling By Invitation

Conditions

  • Hyperpigmentation

Eligibility Criteria

Sex
FEMALE
Age
18 Years - 75 Years
Healthy Volunteers
Accepted

Interventions

  • Facial Toner — DRUG
    Brightening Toner
  • Placebo Toner — OTHER
    Placebo Control Toner

Study Details

The purpose of this study is to assess the efficacy (ability to produce a desired or intended result) of a topical product (applied to the skin) to improve skin lightness, skin condition and appearance (hyperpigmentation \[dark spots\], brightness/radiance \[healthy vibrant appearance\], skin texture \[smoothness\]) on \] the face over a period of eighteen (18) weeks. The data collected may support the company in developing marketing claims for its product.

Key Dates

Start date
Sep 10, 2025
Status verified
Aug 2025
Primary completion
Feb 16, 2026
Completion
Feb 16, 2026

Study Design

Enrollment
40 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Test Product
  • Sham Comparator: Control Product

Primary Outcome Measure

Skin Lightness [ Time Frame: 18 weeks ]

Locations (1)

FacilityCityStateZIPSite coordinators
Validated Claim SupportTeaneckNew Jersey07666-

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Validated Claim Support· Teaneck, NJ

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