Patient Guide: A Study to Learn About the Vaccine RSVpreF In Pregnant Participants With HIV and Their Infants

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 14 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06325657
Status: ACTIVE_NOT_RECRUITING
Condition: Respiratory Syncytial Virus
Phase: PHASE3

Where You Can Participate

This study is available at 14 locations across the country.

Top locations include:
  • • East London, Eastern CAPE
  • • Bloemfontein, FREE State
  • • Benoni, Gauteng
  • • And 11 more locations

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A Study to Learn About the Vaccine RSVpreF In Pregnant Participants With HIV and Their Infants - Join Clinical Trial NCTNCT06325657

How to Join This Clinical Trial - NCTNCT06325657

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
NCTNCT06325657 - 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 14 locations. Find a study site near you:

Clinical Research Site

East London, Eastern CAPE 5241 - South Africa

Status: Contact for availability

Clinical Research Site

Bloemfontein, FREE State 9301 - South Africa

Status: Contact for availability

Clinical Research Site

Benoni, Gauteng 1500 - South Africa

Status: Contact for availability

Clinical Research Site

Boksburg, Gauteng 1459 - South Africa

Status: Contact for availability

Clinical Research Site

Johannesburg, Gauteng 2001 - South Africa

Status: Contact for availability

Clinical Research Site

Johannesburg, Gauteng 2013 - South Africa

Status: Contact for availability

Clinical Research Site

Johannesburg, Gauteng 2093 - South Africa

Status: Contact for availability

Clinical Research Site

Pretoria, Gauteng 0184 - South Africa

Status: Contact for availability

Clinical Research Site

Tshwane, Gauteng 0152 - South Africa

Status: Contact for availability

Clinical Research Site

Ladysmith, Kwazulu-natal 3370 - South Africa

Status: Contact for availability

And 4 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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