Patient Guide: Efficacy, Immunogenicity, and Safety Study of a Respiratory Syncytial Virus Vaccine in Infants and Toddlers

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 130 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06252285
Status: ACTIVE_NOT_RECRUITING
Condition: RSV Immunisation
Phase: PHASE3

Where You Can Participate

This study is available at 130 locations across the country.

Top locations include:
  • • Birmingham, Alabama
  • • Guntersville, Alabama
  • • Tucson, Arizona
  • • And 127 more locations

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Efficacy, Immunogenicity, and Safety Study of a Respiratory Syncytial Virus Vaccine in Infants and Toddlers - Join Clinical Trial NCTNCT06252285

How to Join This Clinical Trial - NCTNCT06252285

Learn how to participate in this PHASE3 trial studying an investigational therapy for RSV Immunisation. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
RSV Immunisation
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT06252285 - 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 130 locations. Find a study site near you:

Clinical Research Site

Birmingham, Alabama 35205-1628 - United States

Status: Contact for availability

Clinical Research Site

Guntersville, Alabama 35976 - United States

Status: Contact for availability

Clinical Research Site

Tucson, Arizona 85741-2306 - United States

Status: Contact for availability

Clinical Research Site

Madera, California 93637 - United States

Status: Contact for availability

Clinical Research Site

Tarzana, California 91356 - United States

Status: Contact for availability

Clinical Research Site

Victorville, California 92395-8306 - United States

Status: Contact for availability

Clinical Research Site

Coconut Creek, Florida 33073 - United States

Status: Contact for availability

Clinical Research Site

Doral, Florida 33122-1088 - United States

Status: Contact for availability

Clinical Research Site

Orlando, Florida 32829 - United States

Status: Contact for availability

Clinical Research Site

Tampa, Florida 33609 - United States

Status: Contact for availability

And 120 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE3 clinical trial for RSV Immunisation:

  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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