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Completed Phase 2 Interventional

Phase 2 Study Evaluating the Safety and Efficacy of Microneedle-mediated Delivery of Doxorubicin (D-MNA) in Patients With Nodular Basal Cell Carcinoma.

ClinicalTrials.gov ID: NCT06608238

Public ClinicalTrials.gov record NCT06608238. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 10, 2026, 7:15 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-blind, Three-arm Phase 2 Study Evaluating Two Dose Levels of Microneedle-mediated Delivery of Doxorubicin Compared With a Device-only Control in Patients With Nodular Basal Cell Carcinoma.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This Phase 2 study evaluates the safety and efficacy of microneedle array (MNA) alone and in combination with two dose levels of doxorubicin (100µg and 200µg) in patients with nodular basal cell carcinoma. Efficacy is assessed using both clinical (visual) and histological endpoints, which together provide a comprehensive evaluation of lesion response.

Study identification

NCT ID
NCT06608238
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
SkinJect, Inc.
Industry
Enrollment
90 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 85 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 2, 2024
Primary completion
Mar 4, 2026
Completion
Mar 12, 2026
Last update posted
May 3, 2026

2024 – 2026

United States locations

U.S. sites
10
U.S. states
7
U.S. cities
9
Facility City State ZIP Site status
Rao Dermotology West Coast -Site #4 Fresno California 93720
Paradigm Research -Site #6 San Diego California 92108
Therapeutics Clinical Research -site 08 San Diego California 92123
Oak Dermotology - site 07 Naperville Illinois 60563
Arlington Dermatology - Site #1 Rolling Meadows Illinois 60008
Clinical Trials Management, LLC- Site #5 Mandeville Louisiana 70448
Rao Dermatology - Site #3 Highlands New Jersey 07716
HIckory Dermatology Research Center Hickory North Carolina 28602
American Skin and Cancer Center - Site#2 Knoxville Tennessee 37909
Virginia Clinical Research Inc - site 11 Norfolk Virginia 23502

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06608238, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 3, 2026 · Synced Sep 10, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06608238 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →