Last updated on November 2018

Lot-to-lot Consistency of Sci-B-Vac in Adults


Brief description of study

A Controlled Trial to Assess the Lot-to-lot Consistency of Sci-B-Vac in Adults

Detailed Study Description

The primary objective of the study is to verify that the manufacturing equivalence of Sci-B-Vac is consistent and to compare the immunogenicity and safety of a three-dose regimen of Sci-B-Vac to a three-dose regimen of Engerix-B in adults.

Clinical Study Identifier: NCT03408730

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Hayes Williams

Accel Research Sites
Birmingham, AL United States

Amina Haggag

Anaheim Clinical Trials
Anaheim, CA United States

Bruce Rankin

Avail Clinical Research
DeLand, FL United States

Mark Kutner

Suncoast Research Group
Miami, FL United States

Nathan Segall

Clinical Research Altanta
Atlanta, GA United States

Mark Turner

Advanced Clinical Research (ACR)
Boise, ID United States

Michael Levin

Clinical Research Center of Nevada
Las Vegas, NV United States

Mary Beth Manning

Rapid Medical Research
Cleveland, OH United States

Carl Griffin

Lynn Health Science Institute
Oklahoma City, OK United States

Judith Kirstein

Advanced Clinical Research (ACR)
Salt Lake City, UT United States

Isabel Leroux-Roels

Universitair Ziekenhuis Gent
Gent, Belgium

Bebi Yassin-Rajkumar, MS

LMC Diabetes & Endocrincology
Toronto, ON Canada

Azhar Toma

Manna Toronto
Toronto, ON Canada

Jeannette Janzen

Manna Montreal
Montreal, QC Canada

Gerald Vallieres

Manna Research Quebec
Quebec City, QC Canada

Michael Manns

Medizinishe Hochschule Hannover
Hannover, Germany

Thomas Berg

Universit tsklinikum Leipzig A R
Leipzig, Germany

Adam Finn

Bristol Royal Hospital for Children
Bristol, United Kingdom

Catherine Cosgrove

St. George's University Hospital NHS Foundation Trust
London, United Kingdom

Dennis Reich, MD

Medicore Research Inc
Sudbury, ON Canada

Maheshi Ramasamy, MD

Oxford University
Oxford, United Kingdom

Saul Faust, MD

Southampton General Hospital
Southampton, United Kingdom