Patient Guide: Brainshuttle AD: A Multiple Ascending Dose Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of RO7126209 Following Intravenous Infusion in Participants With Prodromal or Mild to Moderate 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 45 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04639050
Status: ACTIVE_NOT_RECRUITING
Condition: Alzheimer Disease
Phase: PHASE1, PHASE2

Where You Can Participate

This study is available at 45 locations across the country.

Top locations include:
  • • Atlantis, Florida
  • • Clermont, Florida
  • • Lady Lake, Florida
  • • And 42 more locations

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Brainshuttle AD: A Multiple Ascending Dose Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of RO7126209 Following Intravenous Infusion in Participants With Prodromal or Mild to Moderate Alzheimer's Disease - Join Clinical Trial NCTNCT04639050

How to Join This Clinical Trial - NCTNCT04639050

Learn how to participate in this PHASE1, PHASE2 trial studying an investigational therapy for Alzheimer Disease. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Alzheimer Disease. 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
Treatment Being Tested
Investigational treatment
Study Phase
PHASE1, PHASE2 - Safety and effectiveness study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT04639050 - 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 45 locations. Find a study site near you:

Clinical Research Site

Atlantis, Florida 33462 - United States

Status: Contact for availability

Clinical Research Site

Clermont, Florida 34711 - United States

Status: Contact for availability

Clinical Research Site

Lady Lake, Florida 32159 - United States

Status: Contact for availability

Clinical Research Site

Maitland, Florida 32751 - United States

Status: Contact for availability

Clinical Research Site

Miami, Florida 33135 - United States

Status: Contact for availability

Clinical Research Site

Orlando, Florida 32803 - United States

Status: Contact for availability

Clinical Research Site

Orlando, Florida 32804 - United States

Status: Contact for availability

Clinical Research Site

Stuart, Florida 34997 - United States

Status: Contact for availability

Clinical Research Site

The Villages, Florida 32162 - United States

Status: Contact for availability

Clinical Research Site

Wellington, Florida 33414 - United States

Status: Contact for availability

And 35 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE1, PHASE2 clinical trial for Alzheimer Disease:

  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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