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Completed Phase 2 Interventional Results available

Safety and Efficacy of Two Doses of Anifrolumab Compared to Placebo in Adult Subjects With Active Proliferative Lupus Nephritis

ClinicalTrials.gov ID: NCT02547922

Public ClinicalTrials.gov record NCT02547922. 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 19, 2026, 11:14 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 Multicentre, Randomised, Double-blind, Placebo-controlled, Phase 2 Study Evaluating the Efficacy and Safety of Anifrolumab in Adult Subjects With Active Proliferative Lupus Nephritis

Brief summary

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

The purpose of this study is to evaluate the efficacy and safety of an intravenous treatment regimen of two doses of anifrolumab versus placebo in adult subjects with active proliferative lupus nephritis (LN).

Study identification

NCT ID
NCT02547922
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AstraZeneca
Industry
Enrollment
147 participants

Conditions and interventions

Interventions

Biological · Drug

Eligibility (public fields only)

Age range
18 Years to 70 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
Nov 4, 2015 (Actual)
Primary completion
Nov 26, 2019 (Actual)
Completion
Jan 18, 2021 (Actual)
Last update posted
Nov 24, 2021

2015 – 2021

United States locations

U.S. sites
17
U.S. states
10
U.S. cities
16
Facility City State ZIP Site status
Research Site Glendale Arizona 85306 —
Research Site Phoenix Arizona 85032 —
Research Site La Jolla California 92037-0706 —
Research Site Los Angeles California 90095-1670 —
Research Site Thousand Oaks California 91360 —
Research Site Aurora Colorado 80045 —
Research Site DeBary Florida 32713 —
Research Site Boston Massachusetts 02118 —
Research Site Newark New Jersey 07103-2499 —
Research Site Great Neck New York 11021 —
Research Site New Hyde Park New York 11042 —
Research Site New York New York 10016 —
Research Site New York New York 10029 —
Research Site The Bronx New York 10457 —
Research Site Columbus Ohio 43210 —
Research Site Oklahoma City Oklahoma 73104 —
Research Site Memphis Tennessee 38119 —

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 63 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02547922, 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 Nov 24, 2021 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02547922 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →