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NCT02962960 · ClinicalTrials.gov registry record · Phase 2

A Study to Characterize the Pharmacokinetics, Pharmacodynamics, and Safety of Anifrolumab in Adult Type I Interferon Test High Systemic Lupus Erythematosus Subject With Active Skin Manifestations

A Phase 2 study, sponsored by AstraZeneca.

Completed
Registry status
Phase 2
Development phase
36
Enrollment target

NCT02962960 is a Phase 2 study that has completed, run by AstraZeneca. The registered enrollment target is 36 participants.

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The verdict

NCT02962960, a Phase 2 study, has completed, sponsored by AstraZeneca.

COMPLETED
Registry status
Phase 2
Development phase
36 participants
Enrollment target

Study Summary

This study will be conducted to characterize pharmacokinetics, pharmacodynamics, safety, and tolerability of anifrolumab given via the subcutaneous (SC) route of administration in adult Systemic Lupus Erythematosus (SLE) subjects with a type I Interferon (IFN) test high result and active skin manifestations while receiving Standard of Care (SOC) treatment. In addition, the efficacy of anifrolumab on SLE skin manifestations will be characterized.

Interventions

  • DRUG Placebo
  • DRUG Anifrolumab

Trial Details

FieldValue
Enrollment Target 36 participants
Start Date 2017-02-14
Est. Completion 2018-12-17
Phase Phase 2

Sponsor

AstraZeneca

1,285 total trials

What the Registry Record Tells You About NCT02962960

The ClinicalTrials.gov registry entry for NCT02962960 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 36 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AstraZeneca, which has 1,285 total studies on file at ClinicalTrials.gov.

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

NCT02962960 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02962960 about?

NCT02962960 is a clinical study titled "A Study to Characterize the Pharmacokinetics, Pharmacodynamics, and Safety of Anifrolumab in Adult Type I Interferon Test High Systemic Lupus Erythematosus Subject With Active Skin Manifestations". This study will be conducted to characterize pharmacokinetics, pharmacodynamics, safety, and tolerability of anifrolumab given via the subcutaneous (SC) route of administration in adult Systemic Lupus Erythematosus (SLE) subjects with a type I Interferon (IFN) test high result and active skin manife...

What is the current status of trial NCT02962960?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 36 participants. The study started on 2017-02-14. Estimated completion is 2018-12-17.

What interventions are being tested in trial NCT02962960?

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

Who is sponsoring clinical trial NCT02962960?

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

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.