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COMPLETED Phase 1

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

NCT06345404 · View on ClinicalTrials.gov ↗

Study Summary

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

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG Soquelitinib

Study Locations (16)

California

  • Clinical Site 2 — Fremont
  • Clinical Site 7 — Palo Alto
  • Clinical Site 13 — Pomona

New York

  • Clinical Site 11 — Brooklyn
  • Clinical Site 16 — New York
  • Clinical Site 12 — New York

Pennsylvania

  • Clinical Site 1 — Camp Hill
  • Clinical Site 8 — Philadelphia

Texas

  • Clinical Site 4 — Frisco
  • Clinical Site 14 — San Antonio

Alabama

  • Clinical Site 5 — Birmingham

Arizona

  • Clinical Site 9 — Tucson

Arkansas

  • Clinical Site 3 — North Little Rock

Colorado

  • Clinical Site 10 — Castle Rock

Trial Details

FieldValue
Enrollment Target 82 participants
Start Date 2024-04-16
Est. Completion 2026-02-24
Phase Phase 1

Sponsor

Corvus Pharmaceuticals

5 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06345404

The ClinicalTrials.gov registry entry for NCT06345404 describes a study currently listed as completed. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 82 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Corvus Pharmaceuticals, which has 5 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Atopic Dermatitis appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06345404 reports 16 study locations spanning 10 distinct geographic areas — top geographies include California, New York, Pennsylvania. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06345404 about?

NCT06345404 is a clinical study titled "Safety, Tolerability, and Preliminary Efficacy of Soquelitinib in Participants With Moderate to Severe AD". Safety, tolerability, and preliminary efficacy of soquelitinib in participants with moderate to severe AD

What is the current status of trial NCT06345404?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 82 participants. The study started on 2024-04-16. Estimated completion is 2026-02-24.

What conditions does trial NCT06345404 study?

This clinical trial studies the following conditions: Atopic Dermatitis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06345404?

The interventions under investigation include: Placebo (DRUG), Soquelitinib (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06345404?

This trial is sponsored by Corvus Pharmaceuticals, which has 5 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06345404 being conducted?

This trial has 16 study locations across Alabama, Arizona, Arkansas, California, Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial