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Completed Phase 1Phase 2 Interventional Accepts healthy volunteers Results available

A Single Ascending Dose Study in Adults (Stage 1) and Single Ascending Dose-Finding Study (Stage 2) in Elderly Subjects With ASP3772, A Pneumococcal Vaccine

ClinicalTrials.gov ID: NCT03803202

Public ClinicalTrials.gov record NCT03803202. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 11:51 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1/2, Randomized, Single Ascending Dose Study in Adults (Stage 1) and Randomized, Single Ascending Dose-Finding Study (Stage 2) in Elderly Subjects With ASP3772, a Pneumococcal Vaccine

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of the study is to evaluate the safety, tolerability, and immunogenicity of 3 different dose levels of ASP3772 in comparison to the active comparator Prevnar 13® (PCV13) in adults 18 to 64 years of age in Stage 1. Stage 2 will evaluate the safety, tolerability, and immunogenicity of 3 different dose levels of ASP3772 in comparison to the active comparator PCV13 in elderly 65 to 85 years of age. In addition, Stage 2 will evaluate the immunogenicity of 3 different dose levels of ASP3772 relative to the response seen following administration of Pneumovax® 23 (PPSV23) for the serotypes not included in PCV13.

Study identification

NCT ID
NCT03803202
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
630 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
18 Years to 85 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 24, 2019 (Actual)
Primary completion
Sep 28, 2020 (Actual)
Completion
Sep 28, 2020 (Actual)
Last update posted
Dec 21, 2023

2019 – 2020

United States locations

U.S. sites
26
U.S. states
11
U.S. cities
24
Facility City State ZIP Site status
Advanced Clinical Research-Rancho Paseo Banning California 92220 —
Artemis Institute San Diego California 92103 —
Artemis Institute San Marcos California 92078 —
Research Centers of America Hollywood Florida 33024 —
Meridian Clinical Research Savannah Georgia 31406 —
Sundance Clinical Research St Louis Missouri 63141 —
Meridian Clinical Research Norfolk Nebraska 68701 —
United Medical Associates Binghamton New York 13901 —
PMG Research of Raleigh Raleigh North Carolina 27604 —
PMG Research of Hickory, LLC Rocky Mount North Carolina 27804 —
Piedmont HealthCare, PA Statesville North Carolina 28625 —
Wilmington Health Wilmington North Carolina 28401 —
PMG Research of Winston-Salem, LLC Winston-Salem North Carolina 27103 —
Tekton Research - George Town Yukon Oklahoma 73099 —
PMG Research Knoxville Tennessee 37912 —
PMG Research Knoxville Tennessee 37938 —
Advanced Clinical Research Institute Cedar Park Texas 78613 —
Texas Healthcare, PLLC Fort Worth Texas 76104 —
Benchmark Research Fort Worth Texas 76135 —
Texas Center for Drug Development Houston Texas 77081 —
Healthcare Associatiates of Texas McKinney Texas 75070 —
DM Clinical Research Pearland Texas 77584 —
Benchmark Research San Angelo Texas 76904 —
Clinical Trials of Texas San Antonio Texas 78229 —
Martin Diagnostic Clinic Tomball Texas 77375 —
CRA of Tidewater Inc Norfolk Virginia 23507 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03803202, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 21, 2023 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03803202 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →