Patient Guide: A Follow-up Trial of GBS-NN/NN2 Vaccine in Healthy Pregnant Women

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 5 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06592586
Status: 🟢 Enrolling Now
Condition: Streptococcus Agalactiae Infection, Neonatal Sepsis, Pneumonia, Meningitis, Neonatal Infection, Gram-Positive Bacterial Infections, Bacterial Infections, Bacterial Infections and Mycoses, Infections
Phase: PHASE2, PHASE3

Where You Can Participate

This study is available at 5 locations across the country.

Top locations include:
  • • Aarhus N, Midtjylland
  • • Kolding, Syddanmark
  • • Ga-Rankuwa, Gauteng
  • • And 2 more locations

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A Follow-up Trial of GBS-NN/NN2 Vaccine in Healthy Pregnant Women - Join Clinical Trial NCTNCT06592586

How to Join This Clinical Trial - NCTNCT06592586

Learn how to participate in this PHASE2, PHASE3 trial studying an investigational therapy for Streptococcus Agalactiae Infection, Neonatal Sepsis, Pneumonia, Meningitis, Neonatal Infection, Gram-Positive Bacterial Infections, Bacterial Infections, Bacterial Infections and Mycoses, Infections. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Streptococcus Agalactiae Infection, Neonatal Sepsis, Pneumonia, Meningitis, Neonatal Infection, Gram-Positive Bacterial Infections, Bacterial Infections, Bacterial Infections and Mycoses, Infections. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Streptococcus Agalactiae Infection, Neonatal Sepsis, Pneumonia, Meningitis, Neonatal Infection, Gram-Positive Bacterial Infections, Bacterial Infections, Bacterial Infections and Mycoses, Infections
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2, PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06592586 - 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 5 locations. Find a study site near you:

Clinical Research Site

Aarhus N, Midtjylland 8200 - Denmark

Status: RECRUITING

Clinical Research Site

Kolding, Syddanmark 6000 - Denmark

Status: RECRUITING

Clinical Research Site

Ga-Rankuwa, Gauteng 0204 - South Africa

Status: RECRUITING

Clinical Research Site

Johannesburg, Guateng Province 2001 - South Africa

Status: RECRUITING

Clinical Research Site

Pretoria, Guateng Province 0152 - South Africa

Status: RECRUITING

How to Enroll in This Study

To learn more about participating in this PHASE2, PHASE3 clinical trial for Streptococcus Agalactiae Infection, Neonatal Sepsis, Pneumonia, Meningitis, Neonatal Infection, Gram-Positive Bacterial Infections, Bacterial Infections, Bacterial Infections and Mycoses, Infections:

  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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