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Completed Phase 1 Interventional

Safety, Tolerability, and Preliminary Efficacy of Soquelitinib in Participants With Moderate to Severe AD

ClinicalTrials.gov ID: NCT06345404

Public ClinicalTrials.gov record NCT06345404. 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 Oct 16, 2026, 9:33 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 Phase 1, Randomized, Blinded, Placebo-controlled, Dose Escalation and Expansion Study to Investigate the Safety, Tolerability, and Preliminary Efficacy of ITK Inhibitor Soquelitinib in Participants With Moderate to Severe Atopic Dermatitis

Brief summary

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

Safety, tolerability, and preliminary efficacy of soquelitinib in participants with moderate to severe AD

Study identification

NCT ID
NCT06345404
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Corvus Pharmaceuticals, Inc.
Industry
Enrollment
82 participants

Conditions and interventions

Interventions

Drug

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
Apr 16, 2024 (Actual)
Primary completion
Jan 28, 2026 (Actual)
Completion
Feb 24, 2026 (Actual)
Last update posted
Mar 12, 2026

2024 – 2026

United States locations

U.S. sites
16
U.S. states
10
U.S. cities
15
Facility City State ZIP Site status
Clinical Site 5 Birmingham Alabama 35244 —
Clinical Site 9 Tucson Arizona 85704 —
Clinical Site 3 North Little Rock Arkansas 72117 —
Clinical Site 2 Fremont California 94538 —
Clinical Site 7 Palo Alto California 94063 —
Clinical Site 13 Pomona California 91767 —
Clinical Site 10 Castle Rock Colorado 80109 —
Clinical Site 6 Tampa Florida 33615 —
Clinical Site 11 Brooklyn New York 11203 —
Clinical Site 16 New York New York 10023 —
Clinical Site 12 New York New York 10075 —
Clinical Site 15 Mayfield Heights Ohio 44124 —
Clinical Site 1 Camp Hill Pennsylvania 17011 —
Clinical Site 8 Philadelphia Pennsylvania 19103 —
Clinical Site 4 Frisco Texas 75034 —
Clinical Site 14 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 NCT06345404, 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 Mar 12, 2026 · Synced Oct 16, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06345404 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →