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DAR-901 TB Booster Vaccine to Prevent TB in Adolescents (DAR-PIA)

Primary Purpose

Tuberculosis

Status
Completed
Phase
Phase 2
Locations
Tanzania
Study Type
Interventional
Intervention
DAR-901
Sterile saline placebo
Sponsored by
Dartmouth-Hitchcock Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Tuberculosis focused on measuring Vaccine

Eligibility Criteria

13 Years - 15 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Negative IGRA at baseline -

Exclusion Criteria: Pregnancy, serious underlying disease

-

Sites / Locations

  • Muhimbili University of Health and Allied Sciences

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

DAR-901

Placebo

Arm Description

0.1 mL intradermal injection of 1 mg DAR-901

0.1 mL intradermal injection of sterile saline for human use

Outcomes

Primary Outcome Measures

New Infection With Mycobacterium Tuberculosis
New infection with TB is based on conversion of IGRA

Secondary Outcome Measures

Persistent New Infection With M. Tuberculosis
New positive IGRA that is also positive on repeat ≥3 mos later

Full Information

First Posted
March 14, 2016
Last Updated
April 17, 2021
Sponsor
Dartmouth-Hitchcock Medical Center
Collaborators
Muhimbili University of Health and Allied Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT02712424
Brief Title
DAR-901 TB Booster Vaccine to Prevent TB in Adolescents
Acronym
DAR-PIA
Official Title
A Phase 2, Randomized, Placebo-Controlled, Double-Blind, Study of the Prevention of Infection With Mycobacterium Tuberculosis Among Adolescents Who Have Previously Received BCG
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Completed
Study Start Date
March 2016 (undefined)
Primary Completion Date
February 1, 2020 (Actual)
Study Completion Date
February 1, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Dartmouth-Hitchcock Medical Center
Collaborators
Muhimbili University of Health and Allied Sciences

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
DAR-901 booster vaccine or placebo will be administered to adolescents in Tanzania primed with BCG to determine if immunization reduces the risk of TB infection
Detailed Description
DAR-901 whole cell booster vaccine to prevent TB infection in adolescents ("DAR-PIA") This is a Phase II, 3-injection, randomized, controlled trial of DAR-901 to be conducted in 13-15 year old adolescents in Tanzania previously immunized with BCG. DAR-901 is a whole cell inactivated non-tuberculous mycobacterial vaccine manufactured from the Master Cell Bank of SRL-172 that was used in the successful Phase III DarDar Trial in Tanzania. The goals are to establish the safety and efficacy of DAR-901 in preventing infection with TB. The 1 mg dose was selected during the current Phase I dose-escalation trial of DAR-901 in the US being conducted by Dartmouth and Aeras. The 1 mg dose corresponds to the dose of SRL 172 used in the DarDar Trial. All subjects will be screened by the T-spot® IGRA (Oxford Immunotec, Oxford, England) for evidence of TB infection. All screened subjects will have a structured interview to identify risk factors for TB infection (=positive IGRA). IGRA-positive subjects will be referred for further evaluation and will not be entered in the immunization phase of the trial. It is estimated that 1000 adolescents will need to be screened to identify a total of 650 IGRA-negative adolescents in the immunization phase of the trial. Subjects will be and randomized 1:1 to DAR-901 or saline control at 0, 2 and 4 months. Doses will be administered by intradermal (ID) injection in the deltoid area. IGRA testing will be repeated before dose 2, at 14 months, and again at 24 months. This three year study began in the first quarter of 2016 in Dar es Salaam, is funded by GHIT-Japan and will be directed by Geisel School of Medicine at Dartmouth (PI, F. von Reyn) with collaborators at Muhimbili University of Health and Allied Sciences (MUHAS) in Tanzania and Tokyo Medical and Dental University in Japan.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tuberculosis
Keywords
Vaccine

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
625 (Actual)

8. Arms, Groups, and Interventions

Arm Title
DAR-901
Arm Type
Active Comparator
Arm Description
0.1 mL intradermal injection of 1 mg DAR-901
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
0.1 mL intradermal injection of sterile saline for human use
Intervention Type
Biological
Intervention Name(s)
DAR-901
Intervention Type
Biological
Intervention Name(s)
Sterile saline placebo
Primary Outcome Measure Information:
Title
New Infection With Mycobacterium Tuberculosis
Description
New infection with TB is based on conversion of IGRA
Time Frame
3 years
Secondary Outcome Measure Information:
Title
Persistent New Infection With M. Tuberculosis
Description
New positive IGRA that is also positive on repeat ≥3 mos later
Time Frame
3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
13 Years
Maximum Age & Unit of Time
15 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Negative IGRA at baseline - Exclusion Criteria: Pregnancy, serious underlying disease -
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
C Fordham von Reyn, MD
Organizational Affiliation
Dartmouth-Hitchcock Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Muhimbili University of Health and Allied Sciences
City
Dar es Salaam
Country
Tanzania

12. IPD Sharing Statement

Citations:
PubMed Identifier
33004239
Citation
Munseri P, Said J, Amour M, Magohe A, Matee M, Rees CA, Mackenzie T, Tvaroha S, Bailey-Kellogg C, Maro I, Wieland-Alter W, Adams LV, Horsburgh CR, Nakamura K, Arbeit RD, Pallangyo K, von Reyn CF. DAR-901 vaccine for the prevention of infection with Mycobacterium tuberculosis among BCG-immunized adolescents in Tanzania: A randomized controlled, double-blind phase 2b trial. Vaccine. 2020 Oct 27;38(46):7239-7245. doi: 10.1016/j.vaccine.2020.09.055. Epub 2020 Sep 29.
Results Reference
derived
PubMed Identifier
32811463
Citation
Rees CA, Pineros DB, Amour M, Munseri P, Said J, Magohe A, Matee M, Pallangyo K, von Reyn CF. The potential of CBC-derived ratios (monocyte-to-lymphocyte, neutrophil-to-lymphocyte, and platelet-to-lymphocyte) to predict or diagnose incident TB infection in Tanzanian adolescents. BMC Infect Dis. 2020 Aug 18;20(1):609. doi: 10.1186/s12879-020-05331-w.
Results Reference
derived

Learn more about this trial

DAR-901 TB Booster Vaccine to Prevent TB in Adolescents

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