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Smallpox clinical trials

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NCT ID: NCT02443623 Completed - Clinical trials for Smallpox Vaccine Adverse Reaction

VA-008 ACAM2000® Vaccination of Plasma Donors for the Production of VIGIV

Start date: September 2015
Phase: Phase 4
Study type: Interventional

Objectives: - To vaccinate plasma donors with the ACAM2000 smallpox vaccine thereby inducing an immune response resulting in high anti-vaccinia antibody titers. The collection of donor plasma will be used in the manufacturing of Vaccinia Immune Globulin Intravenous (VIGIV). - To ensure the safety of plasma donors vaccinated with ACAM2000 through the implementation of risk factor screening procedures and the collection of post-vaccination safety data.

NCT ID: NCT02038881 Completed - Smallpox Clinical Trials

Randomized, Open-label Phase II Trial to Assess the Safety and Immunogenicity of MVA-BN Smallpox Vaccine in Immunocompromised Subjects With HIV Infection

Start date: April 28, 2014
Phase: Phase 2
Study type: Interventional

The main purpose of this clinical trial is to generate additional safety data in a highly immunocompromised population. HIV-infected persons are considered excellent candidates to represent the highly immunocompromised population for enrolment in this trial. Additionally, the immune system's response (protection against smallpox as measured by the amount of antibodies produced) following injections of MVA-BN® smallpox vaccine will be evaluated. All participants in this trial will be randomly and evenly assigned to one of three groups to receive two, three or four injections. Group 1 will receive the standard regime consisting of one dose at each vaccination time point, Group 2 will receive two doses at each vaccination time point and Group 3 will receive a booster vaccination 12 weeks after the standard vaccination schedule with MVA-BN® smallpox vaccine. Participation in the trial is scheduled to last up to 75 weeks.

NCT ID: NCT01913353 Completed - Clinical trials for 18-42 Year Old Healthy Vaccinia-naïve Subjects

A Non-inferiority Trial to Compare MVA-BN® Smallpox Vaccine to ACAM2000®

Start date: March 2015
Phase: Phase 3
Study type: Interventional

To demonstrate the efficacy of MVA-BN® in terms of vaccinia-specific Plaque Reduction Neutralization Test (PRNT) antibody response and by showing that vaccination prior to administration of ACAM2000® results in an attenuated take.

NCT ID: NCT01827371 Completed - Smallpox Clinical Trials

Phase II Trial to Assess Safety and Immunogenicity of IMVAMUNE®

Start date: June 2013
Phase: Phase 2
Study type: Interventional

Imvamune (licensed name of MVA being developed as a smallpox vaccine) has been tested in over 2,000 individuals and is on path for licensure. This study will be a Phase II to evaluate three different immunization schedules and two different modes of delivery. The study will look at condensed schedules. Study will randomize subjects to one of four arms.

NCT ID: NCT01668537 Completed - Smallpox Clinical Trials

A Phase II Trial to Compare a Liquid-frozen and a Freeze-dried Formulation of IMVAMUNE (MVA-BN®) Smallpox Vaccine in Vaccinia-naïve Healthy Subjects

Start date: March 2013
Phase: Phase 2
Study type: Interventional

A randomized, double-blind, multicenter Phase II trial to compare the immunogenicity and safety of a liquid-frozen and a freeze-dried formulation of IMVAMUNE (MVA-BN®) smallpox vaccine in vaccinia-naïve healthy subjects

NCT ID: NCT01540929 Completed - Smallpox Clinical Trials

Post-licensure Department of Defense (DOD) Screening Accuracy Study in Military Personnel

Start date: September 2009
Phase:
Study type: Observational

This is a retrospective study of the Department of Defense (DoD) Smallpox Screening Form 600s (SF600s) generated during screening of service members for possible immunization with the ACAM2000® smallpox vaccine. Primary Objective: - To evaluate the accuracy of the DoD smallpox vaccination screening process in military personnel. Secondary Objective: - To describe the number of subjects who are excluded from vaccination, stratified by the pre-defined categories for exclusion (separately for the Screened and Evaluable Populations).

NCT ID: NCT01317238 Completed - Smallpox Clinical Trials

Safety and Efficacy of CJ Smallpox Vaccine in Previously Vaccinated Healthy Volunteers

Start date: October 2010
Phase: Phase 3
Study type: Interventional

The currently available stock of smallpox vaccine would be insufficient in the face of an incident of smallpox attack. Thus, new manufacturing methods for smallpox vaccine are urgently needed because previous manufacturing methods using calf lymph are no longer acceptable in the view of current standards. Recently, CJ corporation in Republic of Korea has developed cell-culture derived smallpox vaccine (CJ-50300) which was manufactured by infecting MRC-5 cells. The aim of this clinical trial were to assess safety, reactogenicity, and immunogenicity of CJ-50300 in previously vaccinated healthy volunteers

NCT ID: NCT01158157 Completed - Clinical trials for Smallpox Vaccine Adverse Reaction

VA-006 Vaccinia Vaccine (ACAM2000) for the Production of VIGIV

Start date: September 13, 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to vaccinate plasma donors with ACAM2000 smallpox vaccine for collection of plasma to be used in the manufacturing of Vaccinia Immune Globulin Intravenous (VIGIV).

NCT ID: NCT01144637 Completed - Smallpox Clinical Trials

A Trial to Evaluate Immunogenicity and Safety of Three Consecutive Production Lots of IMVAMUNE® (MVA-BN®) Smallpox Vaccine in Healthy, Vaccinia-naïve Subjects

Start date: February 2013
Phase: Phase 3
Study type: Interventional

A randomized, double-blind, placebo-controlled Phase III trial to evaluate immunogenicity and safety of three consecutive production lots of IMVAMUNE® (MVA-BN®) smallpox vaccine in healthy, vaccinia-naïve subjects.

NCT ID: NCT01056770 Completed - Smallpox Clinical Trials

Safety and Efficacy of CJ Smallpox Vaccine in Healthy Volunteers

Start date: October 2009
Phase: Phase 3
Study type: Interventional

The currently available stock of smallpox vaccine would be insufficient in the face of an incident of smallpox attack. Thus, new manufacturing methods for smallpox vaccine are urgently needed because previous manufacturing methods using calf lymph are no longer acceptable in the view of current standards. Recently, CJ corporation in Republic of Korea has developed cell-culture derived smallpox vaccine (CJ-50300) which was manufactured by infecting MRC-5 cells. The aim of this clinical trial were to assess safety, reactogenicity, and immunogenicity of CJ-50300.