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Terminated Phase 2 Interventional Results available

Dose Ranging Study of Brentuximab Vedotin in Adults With Lupus

ClinicalTrials.gov ID: NCT02533570

Public ClinicalTrials.gov record NCT02533570. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 25, 2026, 1:25 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multi-center, Randomized, Double-blinded, Placebo-controlled, Multiple-ascending-dose Study of Brentuximab Vedotin in Adults With Active Systemic Lupus Erythematosus

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate the safety and tolerability of brentuximab vedotin in adults with active systemic lupus erythematosus (SLE).

Study identification

NCT ID
NCT02533570
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Seagen Inc.
Industry
Enrollment
20 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 2015 (Type not available)
Primary completion
Jun 5, 2017 (Actual)
Completion
Jun 5, 2017 (Actual)
Last update posted
Jun 11, 2018

2015 – 2017

United States locations

U.S. sites
17
U.S. states
12
U.S. cities
17
Facility City State ZIP Site status
University of Alabama at Birmingham - (UAB) Birmingham Alabama 35294 —
TriWest Research Associates, LLC El Cajon California 92020-4124 —
Advanced Medical Research, LLC La Palma California 90623 —
University of Colorado Aurora Colorado 80045 —
Clinical Research of West Florida - Corporate Clearwater Florida 33765 —
Lakes Research, LLC Miami Lakes Florida 33014 —
Arthritis Associates Orlando Florida 32804 —
McIlwain Medical Group Tampa Florida 33613 —
Henry Ford Health System Detroit Michigan 48202 —
Clayton Medical Associates, P.C. St Louis Missouri 63117 —
Weill Cornell Physicians at Brooklyn Heights Brooklyn New York 11201 —
DJL Clinical Research, PLLC Charlotte North Carolina 28210 —
Arthritis & Rheumatology Center of Oklahoma Oklahoma City Oklahoma 73103 —
Ramesh C Gupta MD Memphis Tennessee 38119 —
Tekton Research, Inc. Austin Texas 78745 —
Accurate Clinical Research Houston Texas 77034 —
Arthritis Clinic of Northern Virginia, PC Arlington Virginia 22205-3606 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02533570, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 11, 2018 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02533570 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →