The federal government
has said it is targeting to commence local manufacturing of COVID-19 vaccines
in the next 12 months.
This is
just as the federal government yesterday said it has concluded the training of
about 40,739 health workers across the nation for the phase two vaccine roll
out.
The
Director General of the National Agency for Food and Drug Administration and
Control (NAFDAC), Prof. Mojisola Adeyeye, who revealed government’s planned
local manufacturing of COVID-19 vaccines while speaking on ARISE News Channel’s
‘The Morning Show,’ also said the agency has commenced clinical trials on three
local herbal medicinal products for the treatment of the virus.
Adeyeye
said the government was concerned about the absence of medicine security and
its implications for the healthcare needs of the people.
She said
the federal government was particularly worried about current challenges posed
by inadequate supply of the vaccines to take care of millions of Nigerians,
adding that the government was working diligently to start local manufacturing
of the vaccine.
When asked
to give update on the plan to establish a factory in Nigeria that would
undertake local manufacturing of COVID-19 vaccines, Adeyeye said: “In terms of
local manufacturing, the federal government is working assiduously to ensure
that there will be local manufacturing of vaccines within a year.”
According
to Adeyeye, with less than two per cent of the country’s population vaccinated
so far, the federal government was conscious of the constraints posed by lack
of drug security.
Adeyeye
further said NAFDAC has initiated a process to develop herbal medicine products
in the country by setting up the Herbal Medicine Product Development Committee
to advance the development of herbal medicine.
She added
that the purpose was to bring herbal medicine practitioners and researchers
together so as to subject their products to scientific investigation.
She
described the development of herbal medicine as a very complicated process.
According
to Adeyeye, NAFDAC undertakes a rigorous process in approving herbal medicines
for the listing by inspecting the premises of the practitioner to ensure that
it meets the required hygienic standards
She also
said the agency runs a number of relevant tests before approving herbal
medicine products for listing.
In
addition, Adeyeye disclosed that NAFDAC has so far commenced clinical trials on
three herbal medicine products with a view to confirming their efficacy for the
treatment of COVID-19.
“Since the
outbreak of COVID-19, we have approved 45 herbal medicines for listing for
temporal approval but you cannot say that they cure COVID-19. Out of these numbers,
two or three herbal medicine products have started clinical trials,” she said.
Adeyeye
said listing a product only means that it is now safe for consumption but does
not confirm how efficacious such a medicine would be until it is subjected to
clinical trials.
“It does
not confirm how efficacious such herbal drug is until it is subjected to
clinical trials. To do clinical trial, it has to be well designed. It is not
just that I gave it to 10 people in my village and it worked, but you have to
do it in such a way that it will attract recognition across the world. That
clinical trial stage is what is going on now,” she said.
Adeyeye
also spoke of the Central Bank of Nigeria assisted initiative known as the
Research and Development Intervention Scheme which provides funds to assist
local production of medicine.
“It cost a
lot of money, that is why the CBN is helping to put some money into this
intervention scheme for those who are successful during the grant review
process,” she added.
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