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TimeSquare Weekly > Blog > Business > Malaria Vaccine Rollout in Africa: A Cautionary Tale
Business

Malaria Vaccine Rollout in Africa: A Cautionary Tale

Time Square Weekly Editorial Team
Last updated: 2024/07/05 at 8:33 AM
Time Square Weekly Editorial Team
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Malaria Vaccine Rollout in Africa: A Cautionary Tale
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Discovering a Milestone in Global Health: The Long Road to a Malaria Vaccine


Imagine if a Malaria Vaccine Had Come Sooner


What if Malaria Shots Arrived 9 Years Ago?


143,000 Lives Saved – The Impact of an Earlier Malaria Vaccine

That’s how many children’s lives could have been spared from preventable deaths.


By Stephanie Nolen

Stephanie Nolen interviewed more than 30 scientists, health officials, and other key players in the development of the malaria vaccines to report this article.

July 5, 2024


Nurses in countries from Sierra Leone to Cameroon are packing a new vaccine into the coolers they tote to villages for immunization clinics: a shot to protect against malaria, one of the deadliest diseases for children.

Babies and toddlers in eight countries in the region recently started to get the vaccine as part of their routine childhood shots. Seven other African countries are eagerly awaiting its arrival.


This is a milestone in global health.

But it’s also a cautionary tale about a system that is ill-equipped to deliver critical tools to the people who need them most.

It took decades and at least a billion dollars to reach this point. Even now, only a fraction of the children whose lives are at risk will get the vaccine this year, or next year, or the year after.

It’s been clear for some time what went wrong, but almost none of those issues have been fixed. That means that the next desperately needed vaccine stands every chance of running into those same problems.

Take, for example, a new vaccine for tuberculosis that started clinical trials a few months ago. If it works as well as hoped, it could save at least a million lives a year. We’ll know by 2028 if it stops tuberculosis infections. But if it follows the same trajectory, it will be at least 2038 before it’s shipped to clinics.

“Children are receiving the vaccine, and for that, I am the happiest man in the world. But on the other hand, I cannot avoid being dismayed at this inexcusably long delay.”

— Dr. Joe Cohen, co-inventor of the first malaria vaccine


The U.S. Army started work on a malaria vaccine back in the 1980s, hoping to protect soldiers deployed to the tropics. It teamed up with the drug company GlaxoSmithKline, and together they produced promising prototypes. But the military lost interest after a few years, and that left GSK with a problem.

The people who desperately needed a malaria vaccine were in villages in sub-Saharan Africa. They would not be able to pay for a product that would cost millions of dollars to develop.

GSK needed an altruistically minded partner. It found one in the nonprofit global health agency PATH, and by the late 1990s they had a vaccine to test. The Bill & Melinda Gates Foundation put up more than $200 million to test it.

The clinical trials were complex because this was a whole new type of vaccine — the first ever against a parasite — delivered to children in places with limited health systems. The process took more than a decade.

Finally, in 2014, results showed this vaccine cut severe malaria cases by about a third.

This was a successful result, but not as much protection as scientists had hoped to see. Still, GSK and PATH planned a production facility to make millions of doses. Gavi, the organization that procures vaccines for low- and middle-income countries, with funds from donors, would buy them.

Then the Gates Foundation pulled its support.

There was a shake-up in the malaria division, and the leadership reoriented toward a new goal: eliminating the disease.

The new malaria team said the vaccine didn’t work well enough to justify pouring millions more dollars into it. It would be better, they said, to wait for a more effective shot in the future, and in the meantime to fund other strategies, such as genetically modifying mosquitoes.

“If you go from very enthusiastic to very unenthusiastic and you’re the Gates Foundation, people pay attention.”

— Dr. Robert Newman, former director, Global Malaria Program, W.H.O.


The decision was driven by researchers who were looking at data. They didn’t factor in that the idea of a vaccine, even one with limited efficacy, would be so important to African parents — and African governments, which would come to see this as a classic example of a paternalistic donor ignoring their priorities. More than 300,000 children died of malaria that year.

The foundation’s announcement shoved the vaccine into limbo — in ways the foundation today says it did not anticipate.

“In hindsight, we could have communicated more often and more clearly about our decisions and listened more clearly to what the impact of those might have been on other institutions and their decisions.”

— Dr. Chris Elias, president of global development at the Bill & Melinda Gates Foundation


GSK and PATH tried to push the vaccine forward. The company submitted a 250,000-page dossier to the European Medicines Agency, which can approve products not relevant in Europe but of humanitarian benefit. In 2015, the agency said the vaccine was safe (with some issues it wanted GSK to continue to study), and PATH began hunting for new financial partners to replace Gates.


Then came a second shock.

The World Health Organization evaluates new vaccines to decide what’s safe and well made, so that countries and Gavi know what to order.

The malaria vaccine needed this sign-off, and since the European agency, a stringent regulator, had approved it, GSK and PATH assumed the W.H.O. would do so swiftly, too.

Two groups met to consider the vaccine for the W.H.O.: an external advisory committee that evaluates vaccines, and a panel of malaria experts.

The malaria specialists, who had seen African hospital wards full of children dying of the disease, said, “Yes, let’s go.”

But the vaccine experts said: No.

They argued that a small increase in cases of meningitis in children who got the shot hadn’t been sufficiently explained. If this small-chance issue turned out to be an actual problem, it could undermine African parents’ confidence in all childhood vaccines, with catastrophic consequences.

Second, they feared that countries might struggle to deliver the vaccine. It came in four doses, none delivered on the usual childhood immunization schedules; the last dose came a year after the third, and without it, the vaccine offered little protection.

In the end, there was a compromise: The W.H.O. announced what it called a pilot implementation, in Kenya, Malawi, and Ghana, that would cost close to $100 million.

“I think that was the right thing. It meant a delay, which was unfortunate. But everyone, including GSK, knew a larger rollout was coming, and they should be ready. Did they act accordingly? I’m afraid not.”

— Dr. Pedro Alonso, former director, Global Malaria Program, W.H.O.


When GSK heard that instead of triumphantly shipping malaria shots to Africa, it would have to put the vaccine through another evaluation, executives ordered that the production facility and the vaccine ingredients be directed to more lucrative products.

“All the manufacturing plans that GSK had put in place were derailed. They stopped manufacturing because they did not want to continue to assume the risk of keeping a facility going for several years at huge expense for a vaccine that they weren’t sure was ever going to see the light of day.”

— Dr. Ashley Birkett, former director of the PATH Malaria Vaccine Initiative


Two years later, the W.H.O. had scraped together funding. GSK restarted a small production line to make enough of the vaccine for the study.

At Gavi, however, board members representing Africa were demanding answers.

When was Africa going to get a vaccine for malaria?

Gavi turned to MedAccess, an organization that provides funding to reduce the financial risk for private companies working on medical products for low-income nations. With MedAccess’ support, Gavi offered a deal to protect GSK from financial risk, saying, in essence, we’ll fund you to start producing, and if the vaccine isn’t approved, we’ll cover the loss.

GSK agreed and kept the production line open.

In the end, the news was good. Data from the pilot showed no safety risk, and the W.H.O. approved the vaccine for Gavi to buy in bulk and ship to Africa. It was December 2021.

But then GSK told Gavi that after all the agony of winning approval, it could produce only 12 million doses of its vaccine each year, tens of millions fewer than anxious countries were hoping for.

Produced by Antonio de Luca

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Time Square Weekly Editorial Team July 5, 2024 July 5, 2024
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