🏛️ Verified NIH Record • Updated 2026-05-27

A Study on the Immune Response and Safety of the Second Dose of an Investigational Chickenpox Vaccine When Given to Healthy Children 3 Months After a First Dose at 12 to 15 Months of Age (NCT06806137)

A Phase 3a, Observer-blind, Randomized, Controlled, Study to Evaluate the Immunogenicity and Safety of an Investigational Varicella Vaccine Compared With Varivax, When Given as a Second Dose to Healthy Children, 3 Months After the Administration of a First Dose at 12 to 15 Months of Age

🟢 Recruiting Phase3 💊 Investigational Drug / Biologic Sponsor: GlaxoSmithKline

🩺 Plain-English Summary (8th-Grade Level)

The purpose of this study is to evaluate the immune response and safety of GSKs investigational varicella vaccine (VNS Vaccine) compared to an already approved varicella vaccine, Varivax (VV), when administered as second dose to healthy children. 3 months after first dose at 12 to 15 months. The study will be conducted in children who have not previously contracted varicella or received a varicella vaccination.

Who can join: Review the eligibility criteria below.

Location: GSK Investigational Site — Salvaleón de Higüey, La Altagracia Province

Age range: 12 Months to 15 Months

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (6 Sites)

  • GSK Investigational Site — Salvaleón de Higüey, La Altagracia Province
  • GSK Investigational Site — Constanza,
  • GSK Investigational Site — Santo Domingo Oeste,
  • GSK Investigational Site — San Pedro Sula,
  • GSK Investigational Site — Tegucigalpa,
  • GSK Investigational Site — Tegucigalpa,

📞 Contact the Study Coordinator

Phone: (877) 379-3718

Email: GSKClinicalSupportHD@gsk.com

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

Explore by condition: All Chickenpox clinical trials

💡 How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
🏛️ View Official NIH Record ↗