LONDON, July 15 (Reuters) - The world's second vaccine
against malaria was launched on Monday as Ivory Coast began a
routine vaccine programme using shots developed by the
University of Oxford and the Serum Institute of India.
The introduction of the World Health Organization
(WHO)-approved R21 vaccine comes six months after the first
malaria vaccine, called RTS,S and developed by British drugmaker
GSK, began being administered in a routine programme in
Cameroon.
Some 15 African countries plan to introduce one of the two
malaria vaccines this year with support from the Gavi global
vaccine alliance.
Ivory Coast has received a total of 656,600 doses of the
Oxford and Serum shot, which will initially vaccinate 250,000
children aged between 0 and 23 months across the West African
country. The vaccine has also been approved by Ghana, Nigeria,
Burkina Faso and the Central African Republic.
The rollout of a second vaccine is the latest milestone in
the global fight against malaria and should help address a
problem that emerged well before either of the two shots was
launched: demand for them is likely to far outstrip supply for
several years.
Experts say having safe and effective malaria vaccines is
important to meet demand. The shot is meant to work alongside
existing tools - such as bed nets - to combat malaria, which in
Africa kills nearly half a million children under the age of
five each year.
The Serum Institute of India, which manufactures the
vaccine, has produced 25 million doses for the initial rollout
of the shot and "is committed to scaling up to 100 million doses
annually", the company said on Monday about the launch in Ivory
Coast.
Serum said it is offering the vaccine for less than $4 per
dose, in keeping with its aim to deliver low-cost vaccines at
scale.
Results from a large trial in February showed the vaccine
prevented around three-quarters of symptomatic malaria cases in
young children the first year after they got the shots.
Experts told Reuters at that time that comparing the two
malaria vaccines head-to-head was difficult because of the many
variables involved in the trials, but overall their performance
was similar - a conclusion endorsed by WHO.