Patient Guide: A Study to Investigate the Immunogenicity and Safety of mRNA-1345 Vaccine Targeting Respiratory Syncytial Virus (RSV) in High-risk Adults

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 44 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06067230
Status: ACTIVE_NOT_RECRUITING
Condition: Respiratory Syncytial Virus
Phase: PHASE3

Where You Can Participate

This study is available at 44 locations across the country.

Top locations include:
  • • Glendale, Arizona
  • • Phoenix, Arizona
  • • Tempe, Arizona
  • • And 41 more locations

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A Study to Investigate the Immunogenicity and Safety of mRNA-1345 Vaccine Targeting Respiratory Syncytial Virus (RSV) in High-risk Adults - Join Clinical Trial NCTNCT06067230

How to Join This Clinical Trial - NCTNCT06067230

Learn how to participate in this PHASE3 trial studying an investigational therapy for Respiratory Syncytial Virus. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Respiratory Syncytial Virus
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT06067230 - 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 44 locations. Find a study site near you:

Clinical Research Site

Glendale, Arizona 85308-5093 - United States

Status: Contact for availability

Clinical Research Site

Phoenix, Arizona 85044-6097 - United States

Status: Contact for availability

Clinical Research Site

Tempe, Arizona 85283-1528 - United States

Status: Contact for availability

Clinical Research Site

Little Rock, Arkansas 72205 - United States

Status: Contact for availability

Clinical Research Site

Los Angeles, California 90095-3075 - United States

Status: Contact for availability

Clinical Research Site

San Diego, California 92103-2209 - United States

Status: Contact for availability

Clinical Research Site

Lakewood, Colorado 80228 - United States

Status: Contact for availability

Clinical Research Site

New Haven, Connecticut 06510-2483 - United States

Status: Contact for availability

Clinical Research Site

Boca Raton, Florida 33434 - United States

Status: Contact for availability

Clinical Research Site

Hialeah, Florida 33012-4170 - United States

Status: Contact for availability

And 34 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 Respiratory Syncytial Virus:

  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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