Patient Guide: A Study to Assess Safety of ABBV-916 and How Intravenous ABBV-916 Moves Through Body and Affects Brain Amyloid Plaque Clearance in Adult Participants (Aged 50-90 Years) With Early Alzheimer's Disease

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 32 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05291234
Status: ACTIVE_NOT_RECRUITING
Condition: Alzheimer's Disease (AD)
Phase: PHASE2

Where You Can Participate

This study is available at 32 locations across the country.

Top locations include:
  • • Tucson, Arizona
  • • Irvine, California
  • • San Diego, California
  • • And 29 more locations

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A Study to Assess Safety of ABBV-916 and How Intravenous ABBV-916 Moves Through Body and Affects Brain Amyloid Plaque Clearance in Adult Participants (Aged 50-90 Years) With Early Alzheimer's Disease - Join Clinical Trial NCTNCT05291234

How to Join This Clinical Trial - NCTNCT05291234

Learn how to participate in this PHASE2 trial studying an investigational therapy for Alzheimer's Disease (AD). Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Alzheimer's Disease (AD). Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Alzheimer's Disease (AD)
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT05291234 - 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 32 locations. Find a study site near you:

Clinical Research Site

Tucson, Arizona 85710-6152 - United States

Status: Contact for availability

Clinical Research Site

Irvine, California 92614 - United States

Status: Contact for availability

Clinical Research Site

San Diego, California 92103-2204 - United States

Status: Contact for availability

Clinical Research Site

San Diego, California 92103 - United States

Status: Contact for availability

Clinical Research Site

Santa Ana, California 92705 - United States

Status: Contact for availability

Clinical Research Site

Aventura, Florida 33180 - United States

Status: Contact for availability

Clinical Research Site

Lady Lake, Florida 32162 - United States

Status: Contact for availability

Clinical Research Site

Lake Worth, Florida 33462-1141 - United States

Status: Contact for availability

Clinical Research Site

Maitland, Florida 32751 - United States

Status: Contact for availability

Clinical Research Site

Melbourne, Florida 32940-8288 - United States

Status: Contact for availability

And 22 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 Alzheimer's Disease (AD):

  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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