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RECRUITING Phase 2

Open Label, Safety and Efficacy Study of QRX003 Lotion in Subjects With Netherton Syndrome

NCT05789056 · View on ClinicalTrials.gov ↗

Study Summary

To assess the safety, tolerability, and efficacy of QRX003 lotion (4%) when added to standard of care treatment regimen, including systemic therapy in subjects with Netherton syndrome

Conditions Studied

Interventions

  • DRUG QRX003, 4% Lotion

Study Locations (4)

California

  • Site #1 — San Diego

Indiana

  • Site #4 — Indianapolis

Massachusetts

  • Site #5 — Quincy

Texas

  • Site #2 — San Antonio

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2023-03-14
Est. Completion 2025-12-30
Phase Phase 2

Sponsor

Quoin Pharmaceuticals

3 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05789056

The ClinicalTrials.gov registry entry for NCT05789056 describes a study currently listed as recruiting. It is categorized as Phase 2, 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 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Quoin Pharmaceuticals, which has 3 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 Netherton Syndrome appearing as the primary indexed condition, and to 1 intervention — of which QRX003, 4% Lotion 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: NCT05789056 reports 4 study locations spanning 4 distinct geographic areas — top geographies include California, Indiana, Massachusetts. 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 NCT05789056 about?

NCT05789056 is a clinical study titled "Open Label, Safety and Efficacy Study of QRX003 Lotion in Subjects With Netherton Syndrome". To assess the safety, tolerability, and efficacy of QRX003 lotion (4%) when added to standard of care treatment regimen, including systemic therapy in subjects with Netherton syndrome

What is the current status of trial NCT05789056?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 20 participants. The study started on 2023-03-14. Estimated completion is 2025-12-30.

What conditions does trial NCT05789056 study?

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

What interventions are being tested in trial NCT05789056?

The interventions under investigation include: QRX003, 4% Lotion (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05789056?

This trial is sponsored by Quoin Pharmaceuticals, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05789056 being conducted?

This trial has 4 study locations across California, Indiana, Massachusetts, Texas. 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