search
Back to results

Invaplex 50 Vaccine Dose-Ranging

Primary Purpose

Diarrhea

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Shigella flexneri 2a Invaplex 50
Sponsored by
U.S. Army Medical Research and Development Command
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for Diarrhea focused on measuring Shigella, diarrhea

Eligibility Criteria

18 Years - 40 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Be in very good health. Exclusion Criteria: Smoker, or have stopped smoking less than one year ago Pregnant History of chronic illnesses, such as: asthma, chronic sinusitis, or chronic seasonal allergies (such as hay fever) Received a vaccination for Shigella or exposure to Shigella bacteria in a research study or through work in a laboratory Positive for HIV, hepatitis B, and hepatitis C by blood test Using anti-diarrheal, anti-constipation, or antacid medications on a regular basis

Sites / Locations

  • Walter Reed Army Institute of Research

Outcomes

Primary Outcome Measures

Safety
Mucosal immune response
Systemic immune response

Secondary Outcome Measures

Full Information

First Posted
April 28, 2004
Last Updated
April 28, 2015
Sponsor
U.S. Army Medical Research and Development Command
search

1. Study Identification

Unique Protocol Identification Number
NCT00082069
Brief Title
Invaplex 50 Vaccine Dose-Ranging
Official Title
Safety and Immunogenicity Study of an Intranasal Shigella Flexneri 2a Invaplex 50 Vaccine
Study Type
Interventional

2. Study Status

Record Verification Date
April 2015
Overall Recruitment Status
Completed
Study Start Date
April 2004 (undefined)
Primary Completion Date
November 2006 (Actual)
Study Completion Date
November 2006 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
U.S. Army Medical Research and Development Command

4. Oversight

5. Study Description

Brief Summary
The vaccine is given as a nose spray. Volunteers will receive a 3-dose vaccination with doses spaced two weeks apart. Volunteers will be assigned to a vaccination group based on their order of enrollment with consideration of their availability to complete the necessary vaccinations and follow-up visits.
Detailed Description
This is an open-labeled dose escalating trial in which a total of 32 subjects (minimum of 24 allowable) will receive one of four intranasal Invaplex 50 vaccine doses according to the following chart: Test articles/dose Group / N* / Invaplex 50 A / 8 / 10 micrograms B / 8 / 50 micrograms C / 8 / 240 micrograms D / 8 / 480 micrograms *minimum of 6 volunteers/group An interval no less than 7 days following the third (and final) dose (total of 35 days between initial dose at the lower dose level and the next initial dose at the next higher dose level) will separate volunteer groups receiving different doses. All volunteers will receive three immunizations. The first dosing time point is Day 0, the second is Day 14 (+- one day), and the third is Day 28 (+- 2 days). Blood and stool specimens will be collected at intervals to examine systemic and mucosal vaccine antigen-specific immune responses. Vaccine safety will be actively monitored during vaccination and for 28 days following the third vaccination dose.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diarrhea
Keywords
Shigella, diarrhea

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
32 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Biological
Intervention Name(s)
Shigella flexneri 2a Invaplex 50
Primary Outcome Measure Information:
Title
Safety
Title
Mucosal immune response
Title
Systemic immune response

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Be in very good health. Exclusion Criteria: Smoker, or have stopped smoking less than one year ago Pregnant History of chronic illnesses, such as: asthma, chronic sinusitis, or chronic seasonal allergies (such as hay fever) Received a vaccination for Shigella or exposure to Shigella bacteria in a research study or through work in a laboratory Positive for HIV, hepatitis B, and hepatitis C by blood test Using anti-diarrheal, anti-constipation, or antacid medications on a regular basis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David Tribble, MD, PhD
Organizational Affiliation
Naval Medical Research Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Walter Reed Army Institute of Research
City
Silver Spring
State/Province
Maryland
ZIP/Postal Code
20910
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
20619378
Citation
Tribble D, Kaminski R, Cantrell J, Nelson M, Porter C, Baqar S, Williams C, Arora R, Saunders J, Ananthakrishnan M, Sanders J, Zaucha G, Turbyfill R, Oaks E. Safety and immunogenicity of a Shigella flexneri 2a Invaplex 50 intranasal vaccine in adult volunteers. Vaccine. 2010 Aug 23;28(37):6076-85. doi: 10.1016/j.vaccine.2010.06.086. Epub 2010 Jul 7.
Results Reference
derived

Learn more about this trial

Invaplex 50 Vaccine Dose-Ranging

We'll reach out to this number within 24 hrs