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NCT01683695 · ClinicalTrials.gov registry record · Phase 1

Safety Study of AMG 557 in Subjects With Lupus Arthritis

A Phase 1 study of Lupus Arthritis, Systemic Lupus Erythematosus, sponsored by Amgen.

Completed
Registry status
Phase 1
Development phase
20
Enrollment target
13
Study locations

NCT01683695 is a Phase 1 study of Lupus Arthritis, Systemic Lupus Erythematosus that has completed, run by Amgen. The registered enrollment target is 20 participants. The trial reports 13 study locations across 7 states.

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The verdict

NCT01683695, a Phase 1 study of Lupus Arthritis, Systemic Lupus Erythematosus, has completed, sponsored by Amgen.

COMPLETED
Registry status
Phase 1
Development phase
20 participants
Enrollment target
13
Study locations

Study Summary

This is a multicenter, randomized, double-blind, parallel, placebo-controlled, multiple dose study that will enroll approximately 40 systemic lupus erythematosus subjects with active lupus arthritis.

Interventions

  • DRUG Matching Placebo
  • DRUG AMG 557

Study Locations (13)

Other

  • Research Site - Odense
  • Research Site - Lille
  • Research Site - Berlin
  • Research Site - Taipei
  • Research Site - Birmingham
  • Research Site - London

California

  • Research Site - Los Angeles
  • Research Site - San Leandro

Connecticut

  • Research Site - Danbury

New York

  • Research Site - Manhasset

New South Wales

  • Research Site - St Leonards

Kuala Lumpur

  • Research Site - Kuala Lumpur

Sarawak

  • Research Site - Kuching

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2012-06
Est. Completion 2016-03
Phase Phase 1

Sponsor

Amgen

558 total trials

What the Registry Record Tells You About NCT01683695

The ClinicalTrials.gov registry entry for NCT01683695 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Amgen, which has 558 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Lupus Arthritis, Systemic Lupus Erythematosus appearing as the primary indexed condition, and to 2 interventions - of which Matching Placebo is the first listed.

NCT01683695 reports 13 study locations spanning 7 distinct geographic areas - top geographies include Other, California, Connecticut.

Frequently Asked Questions

What is clinical trial NCT01683695 about?

NCT01683695 is a clinical study titled "Safety Study of AMG 557 in Subjects With Lupus Arthritis". This is a multicenter, randomized, double-blind, parallel, placebo-controlled, multiple dose study that will enroll approximately 40 systemic lupus erythematosus subjects with active lupus arthritis.

What is the current status of trial NCT01683695?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 20 participants. The study started on 2012-06. Estimated completion is 2016-03.

What conditions does trial NCT01683695 study?

This clinical trial studies the following conditions: Lupus Arthritis, Systemic Lupus Erythematosus.

What interventions are being tested in trial NCT01683695?

The interventions under investigation include: Matching Placebo (DRUG), AMG 557 (DRUG).

Who is sponsoring clinical trial NCT01683695?

This trial is sponsored by Amgen, which has 558 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01683695 being conducted?

This trial has 13 study locations across California, Connecticut, New York, New South Wales, Kuala Lumpur. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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.