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NCT02547922 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study, sponsored by AstraZeneca.

Completed
Registry status
Phase 2
Development phase
147
Enrollment target

NCT02547922: Completed Phase 2 study, sponsored by AstraZeneca.

NCT02547922 is a Phase 2 study that has completed, run by AstraZeneca. The registered enrollment target is 147 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (11% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02547922, a Phase 2 study, has completed, sponsored by AstraZeneca.

COMPLETED
Registry status
Phase 2
Development phase
147 participants
Enrollment target

Study Summary

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).

Primary Outcome

To evaluate the efficacy of anifrolumab plus SOC (combination of mycophenolate mofetil and corticosteroids) compared with placebo plus SOC in subjects with active proliferative lupus nephritis (LN). Geometric mean ratio of 24-hour UPCR at week 52 over baseline. Values \<1 indicate improvement from baseline.

Interventions

  • DRUG Placebo
  • BIOLOGICAL Anifrolumab

Trial Details

FieldValue
Enrollment Target 147 participants
Start Date 2015-11-04
Est. Completion 2021-01-18
Phase Phase 2
AstraZeneca

1,285 total trials

What the finished NCT02547922 record still lists

NCT02547922 is an interventional study that assigns participants to a tested intervention. The registered 147 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (11% higher).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT02547922 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02547922 about?

NCT02547922 is a clinical study titled "Safety and Efficacy of Two Doses of Anifrolumab Compared to Placebo in Adult Subjects With Active Proliferative Lupus Nephritis". 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).

What is the current status of trial NCT02547922?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 147 participants. The study started on 2015-11-04. Estimated completion is 2021-01-18.

What interventions are being tested in trial NCT02547922?

The interventions under investigation include: Placebo (DRUG), Anifrolumab (BIOLOGICAL).

Who is sponsoring clinical trial NCT02547922?

This trial is sponsored by AstraZeneca, which has 1,285 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02547922's enrollment target sits among peer trials

147 495th of 2000 higher than 1,505 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02547922, the US trial registry maintained by the National Library of Medicine. NCT02547922 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.