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COMPLETED Phase 2

A Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Participants With Acne Vulgaris

NCT04856917 · View on ClinicalTrials.gov ↗

Study Summary

Efficacy and Safety of Imsidolimab in Participants with Acne Vulgaris

Conditions Studied

Interventions

  • BIOLOGICAL Placebo
  • DRUG Imsidolimab

Study Locations (15)

Florida

  • Site 10-113 — Sweetwater
  • Site 10-108 — Tampa
  • Site 10-107 — Tampa

Texas

  • Site 10-103 — Austin
  • Site 10-102 — College Station
  • Site 10-101 — San Antonio

California

  • Site 10-111 — Fountain Valley
  • Site 10-106 — Sherman Oaks

Louisiana

  • Site 10-109 — New Orleans
  • Site 10-112 — New Orleans

Arkansas

  • Site 10-114 — Hot Springs

Michigan

  • Site 10-104 — Detroit

New Hampshire

  • Site 10-110 — Portsmouth

Tennessee

  • Site 10-105 — Murfreesboro

Trial Details

FieldValue
Enrollment Target 123 participants
Start Date 2021-05-15
Est. Completion 2022-03-29
Phase Phase 2

Sponsor

Vanda Pharmaceuticals

34 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04856917

The ClinicalTrials.gov registry entry for NCT04856917 describes a study currently listed as completed. 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 123 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vanda Pharmaceuticals, which has 34 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 Acne Vulgaris 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: NCT04856917 reports 15 study locations spanning 9 distinct geographic areas — top geographies include Florida, Texas, California. 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 NCT04856917 about?

NCT04856917 is a clinical study titled "A Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Participants With Acne Vulgaris". Efficacy and Safety of Imsidolimab in Participants with Acne Vulgaris

What is the current status of trial NCT04856917?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 123 participants. The study started on 2021-05-15. Estimated completion is 2022-03-29.

What conditions does trial NCT04856917 study?

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

What interventions are being tested in trial NCT04856917?

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

Who is sponsoring clinical trial NCT04856917?

This trial is sponsored by Vanda Pharmaceuticals, which has 34 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04856917 being conducted?

This trial has 15 study locations across Arkansas, California, Florida, Louisiana, Michigan. 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