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A Study With Self-administered Rocatinlimab in Adolescent and Adult Participants With Moderate-to-severe Atopic Dermatitis
NCT06224192 · View on ClinicalTrials.gov ↗
Study Summary
The primary objective of this study is to assess successful self-administration of rocatinlimab subcutaneously using devices for injection.
Conditions Studied
Interventions
- COMBINATION_PRODUCT Rocatinlimab Prefilled Syringe
- COMBINATION_PRODUCT Rocatinlimab AI
Study Locations (20)
California
- Kern Research Inc — Bakersfield
- Long Beach Research Institute — Long Beach
- Dermatology Research Associates — Los Angeles
- Havana Research Institute Inc — Pasadena
- Integrative Skin Science and Research — Sacramento
Nevada
- Excel Clinical Research — Las Vegas
- Las Vegas Clinical Trials — North Las Vegas
- Skin Cancer and Dermatology Institute — Reno
Florida
- Direct Helpers Research Center — Hialeah
- Anchor Medical Research — Miami
Ohio
- Bexley Dermatology Research — Bexley
- Apex Clinical Research Center LLC — Mayfield Heights
Georgia
- Hamilton Research, LLC — Alpharetta
Idaho
- Treasure Valley Medical Research — Boise
Kansas
- Dermatology and Skin Cancer Center Leawood — Leawood
North Carolina
- The Skin Surgery Center for Clinical Research — Winston-Salem
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 151 participants |
| Start Date | 2024-04-02 |
| Est. Completion | 2026-03-16 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06224192
The ClinicalTrials.gov registry entry for NCT06224192 describes a study currently listed as active not recruiting. It is categorized as Phase 3, 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 151 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Amgen, which has 266 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 Rocatinlimab Prefilled Syringe 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: NCT06224192 reports 20 study locations spanning 12 distinct geographic areas — top geographies include California, Nevada, Florida. 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 NCT06224192 about?
NCT06224192 is a clinical study titled "A Study With Self-administered Rocatinlimab in Adolescent and Adult Participants With Moderate-to-severe Atopic Dermatitis". The primary objective of this study is to assess successful self-administration of rocatinlimab subcutaneously using devices for injection.
What is the current status of trial NCT06224192?
This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 151 participants. The study started on 2024-04-02. Estimated completion is 2026-03-16.
What conditions does trial NCT06224192 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 NCT06224192?
The interventions under investigation include: Rocatinlimab Prefilled Syringe (COMBINATION_PRODUCT), Rocatinlimab AI (COMBINATION_PRODUCT). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06224192?
This trial is sponsored by Amgen, which has 266 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06224192 being conducted?
This trial has 20 study locations across California, Florida, Georgia, Idaho, Kansas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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