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Completed Phase 2 Interventional Results available

A Study of CLE-400 (Topical Gel) for the Treatment of Chronic Pruritus in Adult Subjects With Notalgia Paresthetica

ClinicalTrials.gov ID: NCT06262607

Public ClinicalTrials.gov record NCT06262607. 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 Jul 23, 2026, 1:20 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, Vehicle-controlled, Multicenter, Parallel-Design, Phase 2 Study to Assess the Efficacy and Safety of CLE-400 Topical Gel for the Treatment of Chronic Pruritus in Adult Subjects With Notalgia Paresthetica

Study identification

NCT ID
NCT06262607
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Clexio Biosciences Ltd.
Industry
Enrollment
59 participants

Conditions and interventions

Interventions

  • CLE-400 Drug
  • Vehicle Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 80 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
Jan 28, 2024
Primary completion
Nov 5, 2024
Completion
Nov 18, 2024
Last update posted
Nov 17, 2025

2024

United States locations

U.S. sites
13
U.S. states
10
U.S. cities
13
Facility City State ZIP Site status
Clinical site 11 Bryant Arkansas 72022
Clinical Site 21 Fremont California 94538
Clinical site 01 Coral Gables Florida 33134
Clinical Site 13 Margate Florida 33063
Clinical Site 10 North Miami Beach Florida 33116
Clinical Site 02 Indianapolis Indiana 46250
Clinical Site 23 Methuen Massachusetts 01844
Clinical Site 20 Portsmouth New Hampshire 03801
Clinical Site 15 New York New York 10028
Clinical site 03 High Point North Carolina 27262
Clinical Site 09 Dublin Ohio 43016
Clinical site 16 Houston Texas 77004
Clinical Site 06 San Antonio Texas 78213

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06262607, 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 Nov 17, 2025 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06262607 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →