Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

ACTIVE NOT RECRUITING Phase 3

A Study to Assess Long-term Safety, Tolerability, and Efficacy of Rocatinlimab in Adult and Adolescent Participants With Moderate-to-severe Atopic Dermatitis (AD)

NCT05882877 · View on ClinicalTrials.gov ↗

Study Summary

The primary objective of this study is to describe the long-term safety and tolerability of rocatinlimab in participants with moderate-to-severe AD.

Conditions Studied

Interventions

  • OTHER Placebo
  • DRUG Rocatinlimab

Study Locations (20)

California

  • Kern Research Inc — Bakersfield
  • Hope Clinical Research LLC — Canoga Park
  • West Coast Research LLC — Dublin
  • California Dermatology and Clinical Research Institute — Encinitas
  • First OC Dermatology — Fountain Valley
  • Antelope Valley Clinical Trials — Lancaster
  • Chemidox Clinical Trials Incorporated — Lancaster
  • Long Beach Research Institute — Long Beach
  • University of California Los Angeles — Los Angeles
  • Dermatology Research Associates — Los Angeles
  • Wallace Medical Group Inc — Los Angeles
  • Northridge Clinical Trials — Northridge

Arizona

  • Medical Dermatology Specialists — Phoenix
  • Alliance Dermatology and Mohs Center — Phoenix
  • Affiliated Dermatology — Scottsdale
  • Scottsdale Clinical Trials — Scottsdale

Arkansas

  • Dermatology Trial Associates — Bryant
  • Burke Pharmaceutical Research — Hot Springs
  • Arkansas Research Trials, LLC — North Little Rock

Alabama

  • Cahaba Dermatology and Skin Health Center — Birmingham

Trial Details

FieldValue
Enrollment Target 2,621 participants
Start Date 2023-05-31
Est. Completion 2027-06-30
Phase Phase 3

Sponsor

Amgen

266 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05882877

The ClinicalTrials.gov registry entry for NCT05882877 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 2,621 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 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: NCT05882877 reports 20 study locations spanning 4 distinct geographic areas — top geographies include California, Arizona, Arkansas. 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 NCT05882877 about?

NCT05882877 is a clinical study titled "A Study to Assess Long-term Safety, Tolerability, and Efficacy of Rocatinlimab in Adult and Adolescent Participants With Moderate-to-severe Atopic Dermatitis (AD)". The primary objective of this study is to describe the long-term safety and tolerability of rocatinlimab in participants with moderate-to-severe AD.

What is the current status of trial NCT05882877?

This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 2,621 participants. The study started on 2023-05-31. Estimated completion is 2027-06-30.

What conditions does trial NCT05882877 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 NCT05882877?

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

Who is sponsoring clinical trial NCT05882877?

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 NCT05882877 being conducted?

This trial has 20 study locations across Alabama, Arizona, Arkansas, California. 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