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COMPLETED Phase 4

Safety and Efficacy of Adalimumab (Humira) for Hidradenitis Suppurativa (HS) Peri-Surgically

NCT02808975 · View on ClinicalTrials.gov ↗

Study Summary

The objective of this study was to assess the safety and efficacy of adalimumab prior to surgery in participants with moderate to severe Hidradenitis Suppurativa (HS) who were surgical candidates.

Interventions

  • DRUG Placebo
  • DRUG Adalimumab

Study Locations (20)

Other

  • Fundacion Valle Del Lili /ID# 151565 — Cali
  • Hospital Pablo Tobon Uribe /ID# 152693 — Medellín
  • Fakult Nem Kralovske Vinohrady /ID# 169173 — Prague
  • Polyclinique Courlancy /ID# 157761 — Reims

California

  • Wallace Medical Group, Inc. /ID# 171289 — Beverly Hills
  • Encino Research Center / T. Jo /ID# 171347 — Encino
  • University of California Irvine /ID# 170054 — Irvine

Louisiana

  • Tulane Univ /ID# 168441 — New Orleans

Massachusetts

  • Beth Israel Deaconess Medical Center /ID# 168438 — Boston

Michigan

  • University of Michigan Hospitals /ID# 200667 — Ann Arbor

North Carolina

  • Univ NC Chapel Hill /ID# 168446 — Chapel Hill

Pennsylvania

  • Penn State Hershey Medical Ctr /ID# 168447 — Hershey

Rhode Island

  • Rhode Island Hospital /ID# 168439 — Providence

Trial Details

FieldValue
Enrollment Target 206 participants
Start Date 2016-07-18
Est. Completion 2019-10-16
Phase Phase 4

Sponsor

AbbVie

603 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02808975

The ClinicalTrials.gov registry entry for NCT02808975 describes a study currently listed as completed. It is categorized as Phase 4, 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 206 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AbbVie, which has 603 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 Hidradenitis Suppurativa (HS) 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: NCT02808975 reports 20 study locations spanning 15 distinct geographic areas — top geographies include Other, California, Louisiana. 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 NCT02808975 about?

NCT02808975 is a clinical study titled "Safety and Efficacy of Adalimumab (Humira) for Hidradenitis Suppurativa (HS) Peri-Surgically". The objective of this study was to assess the safety and efficacy of adalimumab prior to surgery in participants with moderate to severe Hidradenitis Suppurativa (HS) who were surgical candidates.

What is the current status of trial NCT02808975?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 206 participants. The study started on 2016-07-18. Estimated completion is 2019-10-16.

What conditions does trial NCT02808975 study?

This clinical trial studies the following conditions: Hidradenitis Suppurativa (HS). These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02808975?

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

Who is sponsoring clinical trial NCT02808975?

This trial is sponsored by AbbVie, which has 603 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02808975 being conducted?

This trial has 20 study locations across California, Louisiana, Massachusetts, Michigan, North Carolina. 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