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Completed Phase 1 Interventional Results available

HEPLISAV-B® in Adults With End-Stage Renal Disease (ESRD) Undergoing Hemodialysis

ClinicalTrials.gov ID: NCT03934736

Public ClinicalTrials.gov record NCT03934736. 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 23, 2026, 11:34 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

An Open-label, Single Arm Study, Evaluating the Immunogenicity and Safety of HEPLISAV-B® in Adults With End-Stage Renal Disease (ESRD) Undergoing Hemodialysis

Brief summary

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

This is an open-label, single arm study design to evaluate HEPLISAV-B® in adults with ESRD who are initiating or undergoing hemodialysis.

Study identification

NCT ID
NCT03934736
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Enrollment
119 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

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

Study timeline

Start date
Apr 22, 2019 (Actual)
Primary completion
Oct 23, 2020 (Actual)
Completion
Sep 15, 2021 (Actual)
Last update posted
Aug 9, 2024

2019 – 2021

United States locations

U.S. sites
20
U.S. states
14
U.S. cities
20
Facility City State ZIP Site status
DaVita Clinical Research or Affiliate Bloomfield Connecticut 06002 —
DaVita Clinical Research or Affiliate Middlebury Connecticut 06762 —
DaVita Clinical Research or Affiliate Hollywood Florida 33021 —
DaVita Clinical Research or Affiliate Ocala Florida 34471 —
DaVita Clinical Research or Affiliate Tampa Florida 33614 —
DaVita Clinical Research or Affiliate Winter Park Florida 32789 —
DaVita Clinical Research or Affiliate Jeffersonville Indiana 47130 —
DaVita Clinical Research or Affiliate Roseville Michigan 48066 —
DaVita Clinical Research or Affiliate Edina Minnesota 55435 —
DaVita Clinical Research or Affiliate Minneapolis Minnesota 55404 —
DaVita Clinical Research or Affiliate Kansas City Missouri 64111 —
DaVita Clinical Research or Affiliate Las Vegas Nevada 89106 —
DaVita Clinical Research or Affiliate The Bronx New York 10461 —
DaVita Clinical Research or Affiliate Asheville North Carolina 28801 —
DaVita Clinical Research or Affiliate Canton Ohio 44718 —
DaVita Clinical Research or Affiliate Philadelphia Pennsylvania 19106 —
DaVita Clinical Research or Affiliate El Paso Texas 79902 —
DaVita Clinical Research or Affiliate San Antonio Texas 78229 —
DaVita Clinical Research or Affiliate Norfolk Virginia 23510 —
DaVita Clinical Research or Affiliate Milwaukee Wisconsin 53227 —

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 NCT03934736, 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 Aug 9, 2024 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03934736 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →