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Completed Phase 2 Interventional Results available

AURA-LV: Aurinia Urinary Protein Reduction Active - Lupus With Voclosporin (AURA-LV)

ClinicalTrials.gov ID: NCT02141672

Public ClinicalTrials.gov record NCT02141672. 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 27, 2026, 1:07 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 Randomized, Controlled Double-blind Study Comparing the Efficacy and Safety of Voclosporin (23.7 mg BID, or 39.5 mg BID) With Placebo in Achieving Remission in Patients With Active Lupus Nephritis

Brief summary

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

To assess the efficacy of 2 doses of voclosporin compared to placebo in achieving complete remission after 24 weeks of therapy in subjects with active lupus nephritis.

Study identification

NCT ID
NCT02141672
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Aurinia Pharmaceuticals Inc.
Industry
Enrollment
265 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 75 Years
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
Jun 2014 (Type not available)
Primary completion
Jul 2016 (Actual)
Completion
Jan 2017 (Actual)
Last update posted
May 18, 2021

2014 – 2017

United States locations

U.S. sites
14
U.S. states
9
U.S. cities
14
Facility City State ZIP Site status
AURA-LV Site Los Angeles California 90095 —
AURA-LV Site Palo Alto California 94305 —
AURA-LV Site Gainesville Florida 32610 —
AURA-LV Site Miami Florida 33165 —
AURA-LV Site Farmington Hills Michigan 48334 —
AURA-LV Site Brooklyn New York 11203 —
AURA-LV Site New York New York 10016 —
AURA-LV Site Chapel Hill North Carolina 27599 —
AURA-LV Site Charlotte North Carolina 28204 —
AURA-LV Site Columbus Ohio 43210 —
AURA-LV Site Hershey Pennsylvania 17033 —
AURA-LV Site Chattanooga Tennessee 37408 —
AURA-LV Site Dallas Texas 75390 —
AURA-LV Site Houston Texas 77030 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 72 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02141672, 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 May 18, 2021 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02141672 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →