Patient Guide: Study to Evaluate the Efficacy, Safety, and Tolerability of an Anti-MTBR Tau Monoclonal Antibody (BMS-986446) in Participants 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 176 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06268886
Status: ACTIVE_NOT_RECRUITING
Condition: Alzheimer Disease, Early Onset
Phase: PHASE2

Where You Can Participate

This study is available at 176 locations across the country.

Top locations include:
  • • Chandler, Arizona
  • • Gilbert, Arizona
  • • Phoenix, Arizona
  • • And 173 more locations

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Study to Evaluate the Efficacy, Safety, and Tolerability of an Anti-MTBR Tau Monoclonal Antibody (BMS-986446) in Participants With Early Alzheimer's Disease - Join Clinical Trial NCTNCT06268886

How to Join This Clinical Trial - NCTNCT06268886

Learn how to participate in this PHASE2 trial studying an investigational therapy for Alzheimer Disease, Early Onset. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Alzheimer Disease, Early Onset
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT06268886 - 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 176 locations. Find a study site near you:

Clinical Research Site

Chandler, Arizona 85226-3732 - United States

Status: Contact for availability

Clinical Research Site

Gilbert, Arizona 85297-0441 - United States

Status: Contact for availability

Clinical Research Site

Phoenix, Arizona 85004 - United States

Status: Contact for availability

Clinical Research Site

Scottsdale, Arizona 85253 - United States

Status: Contact for availability

Clinical Research Site

Scottsdale, Arizona 85258-4595 - United States

Status: Contact for availability

Clinical Research Site

Tucson, Arizona 85718-6522 - United States

Status: Contact for availability

Clinical Research Site

Tucson, Arizona 85718-6632 - United States

Status: Contact for availability

Clinical Research Site

Encino, California 91316-1511 - United States

Status: Contact for availability

Clinical Research Site

Fullerton, California 92835-1040 - United States

Status: Contact for availability

Clinical Research Site

Irvine, California 92614-9403 - United States

Status: Contact for availability

And 166 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 Disease, Early Onset:

  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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