Patient Guide: Lupus Landmark Study: A Prospective Registry and Biorepository

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 21 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05934149
Status: 🟢 Enrolling Now
Condition: Systemic Lupus Erythematosus (SLE), Lupus Nephritis, Neuropsychiatric Systemic Lupus Erythematosus
Phase: Not Specified

Where You Can Participate

This study is available at 21 locations across the country.

Top locations include:
  • • Birmingham, Alabama
  • • Tucson, Arizona
  • • Beverly Hills, California
  • • And 18 more locations

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Lupus Landmark Study: A Prospective Registry and Biorepository - Join Clinical Trial NCTNCT05934149

How to Join This Clinical Trial - NCTNCT05934149

Learn how to participate in this Not Specified trial studying an investigational therapy for Systemic Lupus Erythematosus (SLE), Lupus Nephritis, Neuropsychiatric Systemic Lupus Erythematosus. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Systemic Lupus Erythematosus (SLE), Lupus Nephritis, Neuropsychiatric Systemic Lupus Erythematosus. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Systemic Lupus Erythematosus (SLE), Lupus Nephritis, Neuropsychiatric Systemic Lupus Erythematosus
Treatment Being Tested
Investigational treatment
Study Phase
Not Specified - Research study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT05934149 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 21 locations. Find a study site near you:

Clinical Research Site

Birmingham, Alabama 35205 - United States

Status: RECRUITING

Clinical Research Site

Tucson, Arizona 85714 - United States

Status: RECRUITING

Clinical Research Site

Beverly Hills, California 90210 - United States

Status: RECRUITING

Clinical Research Site

Miami, Florida 33146 - United States

Status: RECRUITING

Clinical Research Site

Atlanta, Georgia 30322 - United States

Status: RECRUITING

Clinical Research Site

Chicago, Illinois 60637 - United States

Status: RECRUITING

Clinical Research Site

Worcester, Massachusetts 01605 - United States

Status: RECRUITING

Clinical Research Site

Saint Louis, Missouri 63130 - United States

Status: RECRUITING

Clinical Research Site

Manhasset, New York 11030 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

New York, New York 10032 - United States

Status: NOT_YET_RECRUITING

And 11 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this Not Specified clinical trial for Systemic Lupus Erythematosus (SLE), Lupus Nephritis, Neuropsychiatric Systemic Lupus Erythematosus:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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