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Completed Phase 2 Interventional Results available

A Study to Evaluate the Anti-pruritic Effectiveness of ASN008 in Adults With Mild to Moderate Atopic Dermatitis

ClinicalTrials.gov ID: NCT05870865

Public ClinicalTrials.gov record NCT05870865. 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 May 18, 2026, 1:03 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, Phase 2 Trial to Evaluate the Anti-pruritic Efficacy, Safety, Tolerability, and Pharmacokinetics of ASN008 in Adults With Mild to Moderate Atopic Dermatitis

Study identification

NCT ID
NCT05870865
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Formation Bio, Inc.
Industry
Enrollment
144 participants

Conditions and interventions

Conditions

Not listed

Interventions

Not listed

Eligibility (public fields only)

Age range
18 Years and older
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
May 2, 2023
Primary completion
Nov 26, 2023
Completion
Dec 27, 2023
Last update posted
May 15, 2025

2023

United States locations

U.S. sites
23
U.S. states
15
U.S. cities
23
Facility City State ZIP Site status
TrialSpark Investigative Site 0106 Scottsdale Arizona 85255
TrialSpark Investigative Site 0118 Hot Springs Arkansas 71913
TrialSpark Investigative Site 0123 Beverly Hills California 90212
TrialSpark Investigative Site 0113 Fremont California 94538
TrialSpark Investigative Site 0101 Los Angeles California 90057
TrialSpark Investigative Site 0103 Miami Lakes Florida 33014
TrialSpark Investigative Site 0129 Miramar Florida 33027
TrialSpark Investigative Site 0131 Clarksville Indiana 47129
TrialSpark Investigative Site 0109 Indianapolis Indiana 46250
TrialSpark Investigative Site 0112 Louisville Kentucky 40241
TrialSpark Investigative Site 0108 Baton Rouge Louisiana 70808
TrialSpark Investigative Site 0124 Monroe Louisiana 71201
TrialSpark Investigative Site 0107 Auburn Hills Michigan 48326
TrialSpark Investigative Site 0102 Saint Joseph Missouri 54506
TrialSpark Investigative Site 0115 Kew Gardens New York 11415
TrialSpark Investigative Site 0119 New York New York 10075
TrialSpark Investigative Site 0105 Wilmington North Carolina 28405
TrialSpark Investigative Site 0125 Mason Ohio 45040
TrialSpark Investigative Site 0127 Oklahoma City Oklahoma 73170
TrialSpark Investigative Site 0122 Philadelphia Pennsylvania 19103
TrialSpark Investigative Site 0121 Houston Texas 77056
TrialSpark Investigative Site 0130 Pflugerville Texas 78660
TrialSpark Investigative Site 0114 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 NCT05870865, 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 15, 2025 · Synced May 18, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05870865 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →