This document summarizes an innovative malaria vaccine in development. It uses a whole organism approach with Plasmodium berghei that has shown over 90% protection in early trials. The vaccine aims to address current limitations like lack of efficacy, safety concerns, and inability to prevent the most common parasite, P. vivax. It has received over $2 million in funding and prizes. Clinical trials are expected to begin by late 2015 with the goal of market entry by 2025. Near term, a cryopreservation technology for vaccine storage and delivery is targeting market entry by 2016 with projected annual revenues of $100,000.
2. Company
Research
spin-off of IMM
founded in 2013
Faculdade de Medicina da
Universidade de Lisboa,
Centro Hospitalar Lisboa-Norte,
1649 – 028
Lisboa, Portugal
MCRC Lisboa
NIPC: 513226478
3. Scientific advisory board
Prof. Dr. Robert W. Saurwein
Prof. Chris J. Janse
Prof. Sangeeta N. Bhatia
Dr. Shahid M. Khan
Dr. Inigo A-Barturen
Business development
advisorsFounders
4. Validation
Phase I funding
100 thousand US$
(November 2010)
Phase II funding
1.2 million US$
(November 2013)
Supplement to
Phase II funding
320 thousand US$
(December 2014)
1st
IBERIAN project to receive
Phase II funding by BMGF
5. Business development
1st
prize in BES
innovation contest
(December 2013)
80 thousand US$
Honorable mention in
2013 BGI IUL-MIT
competition
Finalist of the 6th
Universal Biotech
innovation Prize
Finalist of the XII
EVERIS Foundation
7. Problem
MALARIA
2.5 billion people at risk
of contracting malaria
700 thousand deaths
every year
12 billion US$ in lost
GDP of endemic countriesNO EFFECTIVE VACCINE
AVAILABLE
Photo credit: Antonio M. Mendes
Most advanced
candidate only affords
~36% protection against
a single parasite species
8. 4.5 billion
US$ global
market
Humanitarian market:
(estimated value: 3 billion US$)
Private market:
(estimated value: 700 million US$)
Tourist & military
market:
(estimated value: 800 million US$)
Market potential
Photo credit: NYtimes
9. Do not target the most prevalent
parasite, P. vivax
Serious safety
concerns
Vaccine Approaches
Extremely high
dosages
Whole
organism
vaccines
Shown to confer
>90% sterile
protection against a
new infection in
Phase I/IIa trialsMandatory high biosafety BSL3
production facilities
11. Phase I/IIa Clinical trials
Submission of
authorization
request to
regulatory
authorities
Efficacy studies in non-human
primate model
Pharmacological studies in
rabbit model
Expected start
date: End of 2015