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Second Generation Vaccines: The next stage of coronavirus recovery

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The news that the European Union isn’t planning to renew its COVID-19 vaccine contract with AstraZeneca comes as little surprise to anyone who has followed the mess of recriminations, lawsuits, delivery delays and back and forth over concerns about safety and efficiency which have plagued the rollout of the Anglo-Swedish firm’s vaccine, writes Louis Auge.

Just last week, Europe’s medicines regulator (EMA) said it was reviewing reports of a rare nerve condition in people who had received the vaccine; the UK’s medicines regulator has already promised an alternative vaccine to most adults under the age of 40 years old, while some EU member states, such as Denmark, have given up entirely on the AstraZeneca jab.

Seeking to avoid a repeat of its early-stage vaccine rollout struggles, the EU recently inked a massive deal with Pfizer to make clear that jettisoning AstraZeneca won’t damage the bloc’s ability to provide booster doses as necessary. According to the new agreement—the largest COVID-19 vaccine deal so far—the EU will secure up to 1.8 billion doses of the Pfizer-BioNTech jab between now and 2023.

"[The contract] will secure the doses necessary to give booster shots to increase our immunity against the virus. It will provide vaccines adapted to escape variants that no longer respond to the vaccines,” European Commission President Ursula von der Leyen said of the deal. “It should enable us to vaccinate, if necessary and safe, children and teenagers. And it will consolidate Europe's leadership in mRNA technologies.”

The costly deal—reports have suggested that the total agreement is worth €35 billion, with each individual dose costing as much as €4 higher than in previous agreements with Pfizer—underscores the pattern of wealthy nations dipping into their deep pockets to secure vaccines for their populations at any cost.

Pfizer’s mRNA vaccine is one of the most effective COVID-19 jabs currently on the market, but it is also one of the most expensive and logistically difficult to manage. Vaccines using mRNA technology are typically three to four times more expensive than the AstraZeneca shot, which is currently being manufactured on a not-for-profit basis, and initiallyneeded to be stored at low temperatures. For this reason, alternatives to the AstraZeneca vaccine have remained out of reach for many countries, especially developing nations—sparking concerns that a two-tiered society may emerge in the wake of the pandemic.

“If wealthy countries say they are only going to have 'gold standard' with the most expensive vaccines,” explained Dr. Peter Drobac at Oxford Saïd Business School, “and then say AstraZeneca is not good enough for us in the global north, but it is good enough for the global south, it could reduce uptake of the vaccine and hamper efforts to vaccinate the world.” It is encouraging, then, that several companies are already making progress on the much-needed second generation of Covid vaccines, developing a number of promising candidates which may overcome the cost and storage roadblocks which many developing countries are facing.

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Massachusetts-based Akston Biosciences, for example, has embarked on a Phase I/II clinical trial of its vaccine candidate AKS-452 at one of the Netherlands’ largest hospitals. AKS-452 has already shown “robust protection” in primate trials, and has several major advantages: the vaccine retains its potency for at least four months at 25°C, is shelf-stable for shorter periods at 37°C, and can be produced rapidly with standard, low-cost manufacturing techniques. According to Akston Biosciences, a single 2,000 litre production line could produce more than one billion doses in a year.

Akston Biosciences is hoping to first get AKS-452 approved in the EU, but the vaccine candidate could quickly become a vital boost to vaccine rollouts in the developing world. Indeed, the fact that AKS-452 does not require refrigeration or special handling makes it an ideal solution for the over 1 billion people living in sub-Saharan Africa, where electricity can be unreliable or wholly unavailable.

Hopes are also rising after Pennsylvania-based Inovio released very encouraging results from a mid-stage clinical trial for its vaccine candidate, INO-4800, which is the only nucleic acid-based vaccine which is stable at room temperature and even higher temperatures. The firm now plans to file preliminary results with the Food and Drug Administration (FDA).

“Our Phase two results validate our initial Covid-19 Phase one results in a larger population, which show that INO-4800 continues to be generally safe, well-tolerated and immunogenic in all studied age groups,” Inovio’s Dr. Laurent M. Humeau announced this week.

As harrowing footage from India’s second wave brings home the reality of the devastation beyond the first world, the injustice of current vaccine distribution patterns can feel like a knife to the heart. While wealthy countries like those in the EU may have the funds to lock up billions of doses of Covid-19 vaccines, less than 10% of India’s population is currently inoculated against Covid-19— this despite the fact that domestically produced jabs have been exported in their millions beyond Indian shores.

With their substantially lower barriers to distribution, the coming second generation of vaccines may ultimately prove to be the real watershed moment in the global fight against COVID-19. After all, no country will truly be safe until transmission of the virus is brought down all over the world.

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EU Reporter publishes articles from a variety of outside sources which express a wide range of viewpoints. The positions taken in these articles are not necessarily those of EU Reporter.

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