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Support to Research and Development at the International AIDS Vaccine Initiative

Development Objective

The Project Development Objective is to support the International AIDS Vaccine Initiative (IAVI) in the optimization and testing of one HIV vaccine candidate.

Key Details

Project Details

  • P161232

  • Closed

  • Robert Oelrichs

  • International AIDS Vaccine Initiative

  • World

  • August 22, 2016

  • (as of board presentation)

    February 10, 2017

  • February 27, 2017

  • US$ 2.00 million

  • International AIDS Vaccine Initiative

  • Other

  • 2017

  • US$ 1.80 million

  • B

  • Not Applicable

  • September 30, 2018

  • BANK APPROVED

  • August 11, 2022

  • Notes

Finances

Financing Plan (US$ Millions)

No data available.
Financier Commitments
Free-standing TFs for HDNVP 1.80

Total Project Financing (US$ Millions)

Product Line IBRD/IDA
IBRD Commitment N/A
IDA Commitment N/A
IBRD + IDA Commitment N/A
Lending Instrument
Grant Amount 1.80
Total Project Cost** 2.00

Summary Status of World Bank Financing (US$ Millions) as of July 31, 2025

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No data available.
Financier Approval Date Closing Date Principal Disbursed Repayments Interest, Charges & Fees

Detailed Financial Activity as of July 31, 2025

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No data available.
Period Financier Transaction Type Amount (US$)

Footnotes

Ratings

IMPLEMENTATION RATINGS

Name Review Date
Progress towards achievement of PDO Satisfactory 2018-09-26
Overall Low 2018-09-26
Overall Implementation Progress (IP) Satisfactory 2018-09-26

COMPLETION RATINGS

INDICATORIMPLEMENTATION COMPLETION & RESULTS REPORT: 04-11-2019
OutcomesHighly Satisfactory
Risk to Development Outcome
Bank PerformanceHighly Satisfactory
Borrower Performance
Government Performance
Implementing Agency

INDEPENDENT EVALUATION RATINGS

No data available.

Results Framework

PROJECT DEVELOPMENT OBJECTIVE INDICATORS

INDICATORBASELINECURRENTTARGET
  • Vector has been optimizedValueNoYesYes
    DateJuly 4, 2016June 30, 2017June 30, 2017
    Comment
  • Vector testing has been initiatedValueNoYesYes
    DateJuly 4, 2016June 30, 2017June 30, 2017
    Comment
  • VSVdG-Env.BG505.1 vaccine vector has been evaluatedValueNoNoYes
    DateSeptember 6, 2017June 30, 2018June 30, 2018
    Comment
  • Additional viral vectors have been developedValueNoNoYes
    DateSeptember 6, 2017September 28, 2019June 30, 2018
    Comment

INTERMEDIATE RESULTS INDICATORS

INDICATORBASELINECURRENTTARGET
  • Five genetically modified VSVdG-Env.BG505 vaccines have been isolated and characteristics have been analyzedValueNoYesYes
    DateFebruary 10, 2017June 30, 2017June 30, 2017
    Comment
  • VSVdG-Env.BG505 mutants have been isolated after serial passage under conditions that select for viruses with increased replicativefitness. Mutant virus characteristics have been analyzed.ValueNoYesYes
    DateFebruary 10, 2017June 30, 2017June 30, 2017
    Comment
  • Candidate vaccines have been produced for a preclinical study.ValueNoYesYes
    DateFebruary 10, 2017June 30, 2017June 30, 2017
    Comment
  • A decision to test new VSVdG-Env.BG505 vaccines or revise a macaque study to evaluate the requirement for three doses have been made.ValueNoYesYes
    DateFebruary 10, 2017June 30, 2017June 30, 2017
    Comment
  • Preclinical study in non-human primates has been commenced.ValueNoYesYes
    DateFebruary 10, 2017June 30, 2017June 30, 2017
    Comment
  • Determination of construction feasibility and replicative capacity of VSVdG-Env.BG505 with Env in position 2, 3 or 5ValueNoNoYes
    DateJune 20, 2017April 2, 2018June 30, 2018
    Comment
  • VSVdG-Env.BG505 position 1 vector with Matrix protein (M) modifications that will dampen the innate immune response rescuedValueNoNoNo
    DateJune 20, 2017January 1, 2018September 28, 2018
    Comment
  • VSVdG-Env.BG505.1 vector with M modifications evaluated for genetic stability and replicative capacityValueNoNoNo
    DateJune 20, 2017September 28, 2018September 28, 2018
    Comment
  • Initiate VSVdG-Env.BG505 position 1 vector vaccine rescue in Early Development LaboratoryValueNoNoNo
    DateJune 20, 2017September 28, 2018September 28, 2018
    Comment
  • Feasibility of VERO-CD4/CCR5 cell line also expressing VSV glycoprotein G is demonstratedValueNoNoYes
    DateJune 20, 2017December 29, 2017June 30, 2018
    Comment
  • Conduct serial passage of VSV New Jersey vector to improve replicative capacity and fitness of the virusValueNoNoYes
    DateJune 20, 2017December 29, 2017June 30, 2018
    Comment
  • Evaluate VSV New Jersey vector for improved fitness and utility as a vaccine platformValueNoNoYes
    DateJune 20, 2017September 28, 2018June 30, 2018
    Comment
  • Initiate VERO CD4/CCR5 VSV G expressing cell line in Early Development LaboratoryValueNoNoNo
    DateSeptember 6, 2017September 28, 2018September 28, 2018
    Comment
  • Organize and facilitate meeting in conjunction with UHC Forum in December in Tokyo on Japanese investments in global health R&DValueNoNoYes
    DateSeptember 6, 2017January 1, 2018June 30, 2018
    Comment