Patient Guide: A Study to Assess the Safety, Tolerability, and Efficacy of IMVT-1402 in Participants With Cutaneous Lupus Erythematosus (CLE)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 70 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06980805
Status: 🟢 Enrolling Now
Condition: Subacute Cutaneous Lupus Erythematosus, Chronic Cutaneous Lupus Erythematosus
Phase: PHASE2

Where You Can Participate

This study is available at 70 locations across the country.

Top locations include:
  • • Anniston, Alabama
  • • Birmingham, Alabama
  • • Phoenix, Arizona
  • • And 67 more locations

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A Study to Assess the Safety, Tolerability, and Efficacy of IMVT-1402 in Participants With Cutaneous Lupus Erythematosus (CLE) - Join Clinical Trial NCTNCT06980805

How to Join This Clinical Trial - NCTNCT06980805

Learn how to participate in this PHASE2 trial studying an investigational therapy for Subacute Cutaneous Lupus Erythematosus, Chronic Cutaneous Lupus Erythematosus. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Subacute Cutaneous Lupus Erythematosus, Chronic Cutaneous 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
Subacute Cutaneous Lupus Erythematosus, Chronic Cutaneous Lupus Erythematosus
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06980805 - 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 70 locations. Find a study site near you:

Clinical Research Site

Anniston, Alabama 36207-4780 - United States

Status: RECRUITING

Clinical Research Site

Birmingham, Alabama 35203-4050 - United States

Status: RECRUITING

Clinical Research Site

Phoenix, Arizona 85037 - United States

Status: RECRUITING

Clinical Research Site

Scottsdale, Arizona 85260 - United States

Status: RECRUITING

Clinical Research Site

Beverly Hills, California 90211 - United States

Status: RECRUITING

Clinical Research Site

Chula Vista, California 91910 - United States

Status: RECRUITING

Clinical Research Site

Fremont, California 94538 - United States

Status: RECRUITING

Clinical Research Site

Los Angeles, California 90045 - United States

Status: RECRUITING

Clinical Research Site

Aurora, Colorado 80045-2541 - United States

Status: RECRUITING

Clinical Research Site

Castle Rock, Colorado 80109-8034 - United States

Status: RECRUITING

And 60 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE2 clinical trial for Subacute Cutaneous Lupus Erythematosus, Chronic Cutaneous 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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