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03-12-2020
Covid-19 Vaccines: Everything you need to know
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Behind the Headlines: Vaccine analysis


The UK has become the first country in the world to approve a Covid-19 vaccine candidate based on an independent review of large-scale trial data. While this is fantastic news and a vital step towards the country's economic and social recovery, scientists and public health officials are clear that this is the beginning, not the end, of that road. Health Secretary Matt Hancock has said current restrictions will not be loosened until phase 1 vaccination (approximately 30 million people) is complete. 


Speaking at the Downing Street briefing on 2nd December 2020, Jonathan Van-Tam called for the UK to be ‘patient and realistic’ about the speed with which this will happen: supply of the approved Pfizer BioNTech vaccine is limited and rollout will be challenging, not least because it must be stored at -70 degrees centigrade. If phase 1 is to be completed (as is hoped) by the spring, at least one additional vaccine candidate will need to come online before the New Year. 


Employers running routine asymptomatic testing to prevent workplace outbreaks will likely need to continue until at least April 2021; as will those preparing to kick off programmes in the wake of Christmas household mixing.


Vaccine candidates: the current UK situation


There are around 200 vaccines in development globally. To date, the UK Government has agreed access to a total of 357 million doses from 7 different producers. However, it is the trial results from the three ‘front-runners’ (Pfizer BioNTech, Oxford University AstraZeneca and Moderna) that have dominated the headlines in recent weeks.


Of these, the Pfizer BioNTech vaccine and the Oxford/Astra Zeneca vaccine have both been approved by the UK’s Medicines and Healthcare products Regulatory Agency (MHRA). Moderna’s vaccine candidate would not be available in the UK until the spring and as such there has been no formal request from the government for it to undergo emergency assessment. The four remaining candidates are still some way from approval: Novavax, GSK / Sanofi Pasteur and Janssen all have vaccines in phase 3 or 2/3 trials with interim results expected during Q1 2021, after which (assuming they are successful), approval could be sought. Valvena’s vaccine candidate is still in preclinical trials.


The UK has agreed access to 40 million doses of the Pfizer/BioNTech vaccine, which requires two shots, three weeks apart and gives protection 28 days after the first. 800,000 doses are currently being brought in from Belgium and, with rollout beginning next week, the first batch of recipients should be protected from Covid-19 by early-mid January. A further 10 million doses were scheduled to arrive by the end of the year, however this number was revised down to ‘several million’ during the Downing Street press conference yesterday evening. The remainder are due between January and June 2021, depending on availability - the US and EU regulators are also both likely to approve Pfizer's candidate in the coming weeks.


The Oxford vaccine requires two shots, at least four weeks apart, with protection from approximately 14 days after the second. The UK has pre-ordered 100 million doses and expects 4 million to be available pre-Christmas. The Wrexham lab in which the Oxford vaccines will be manufactured is currently gearing up to produce 150,000 doses per day.  The first recipients of the Oxford vaccines have already received their first doses.


Vaccine


Key data: the three front-runner vaccines


Pfizer and BioNTech vaccine BNT162b2
Status: 
Approved by MHRA, December 2nd 2020

What is it and how does it work?: A synthetic mRNA or ‘messenger’ vaccine. Instead of introducing a weakened or dead virus into the body to provoke an immune response, this candidate introduces a ‘messenger’ sequence, constructed from SARS-CoV-2's genetic code and encased in a fat bubble, which essentially uses the body’s own cells as a factory to produce the SARS-CoV-2 spike protein. This then triggers an immune response.

Dosage two doses, 3 weeks apart with protection from 28 days after first inoculation.  The UK has since decided on a second dose being given up to 12 weeks after the first dose.

Efficacy: 95%

Trial Data: Over 43,000 participants enrolled in the trial worldwide and efficacy was consistent across age, gender, race and ethnicity demographics. 170 Covid-19 cases were confirmed with 162 in the placebo group. Ten of the cases were severe, of which one was in the vaccinated group.

Trial press release can be found here

How many doses has the UK secured access to? 40 million

When will they be available? some before Christmas with the majority expected in the first half of 2021

Manufacturing: Germany and Belgium
Storage minus 70 degrees centigrade; 5 days at fridge temperature

Cost:  £15 / a dose


The University of Oxford AstraZeneca vaccine: ChAdOx1 nCoV-19

Status: Approved by MHRA, December 30th 2020 

What is it and how does it work? A vector-based vaccine developed using a weakened adenovirus that causes the common cold in chimpanzees. The virus is genetically altered so as to be impossible to grow in humans; 20% of its genetic instructions are then deleted and replaced with instructions from the SARS-CoV-2 spike protein. When the vaccine enters the body, it reproduces the spike protein to mimic a natural infection and provoke an immune response.

Dosage: Two full doses, at least 4 weeks apart or a half dose followed by a full dose 4 weeks later - protection from 14 days or more after receiving two doses of the vaccine
Efficacy: 
62-90% (70% average)

Trial data: Interim data combined from phase 2/3 trials reports 131 Covid-19 cases across 11,636 participants in the UK and Brazil. 30 cases were confirmed in participants who had been vaccinated but there were no hospitalised or severe cases of Covid-19 in any vaccine recipients. Efficacy in the group receiving two full doses was 62% - significantly lower than Pfizer's but potentially high enough for approval (for context, the US regulator's minimum requirement is 50%). Interestingly, approximately a third (2,741) of the UK trial participants, all under the age of 55, were mistakenly administered a half dose in the first instance, followed by a full dose the second time around - a mistake that seems to have resulted in an efficacy of 90% and could be down to a lower initial dose more closely mimicking the progress of a real infection. Confirmatory data is continuing to be gathered.

Trial press release can be found here

How many doses has the UK secured access to? 100 million
When will they be available: 
if approved, 4 million are expected to be available in December and a further 40 million by the end of March 2021

Manufacturing: capability currently being set up in 10 countries including the UK

Storage fridge at 2-8 degrees centigrade

Cost: approx. £3 per dose


Moderna and US National Institutes of Health mRNA-1273

Status: phase 3 trial complete

What is it and how does it work? An mRNA vaccine, as described above.

Efficacy: 94% (100% protection against severe disease)

Trial data: Primary analysis of the phase 3 data reports 196 Covid-19 cases in 30,000 US participants. Half were given the vaccine, half the placebo. Of the people who became symptomatically ill with Covid-19, 30 had serious illness and one person died however none of these 30 were in the vaccinated group. Efficacy seems consistent across and, race and ethnicity and gender demographics.

Trial press release can be found here.

How many doses has the UK secured access to? 7 million
When will they be available: spring 2021 at the earliest

Manufacturing: Switzerland and the US

Storage: -20 for up to 6 months; fridge for 30 days

Cost £25 / dose


FAQs


Who will get the vaccine first?

The Joint Committee on Vaccination and Immunisation (JCVI) has advised the Government that Phase 1 rollout (approximately 30 million people) should include those who are most likely to become severely ill or die from Covid-19. Vaccination will start with care home residents and workers, followed by frontline health workers and those who are 80+ ; next will be the age groups (in descending order) down to 65, then people aged 16-64 with underlying health conditions and finally the age groups (in descending order again) down to 50. 


Phase two is likely to focus on further reducing hospitalisation and ‘targeted vaccination of those at high risk of exposure and/or those delivering key public services.’ Although the JCVI will not be stipulating which occupations should be prioritised, this is considered to be a policy matter, they suggest this may include "first responders, the military, those involved in the justice system, teachers, transport workers and those essential to the pandemic response." It is therefore likely that the majority of non-health/care employees in the private sector will wait well into 2021 before being offered a vaccine.


Will a vaccine be available privately in the UK?

Although private healthcare companies are permitted to source vaccines from manufacturers, supply is likely to be a major issue in the short term. Pfizer is reported to have confirmed that it will not be selling its vaccine to individuals outside of any UK government roll out. In November, a ministerial source at the Department of Health is reported to have said “everyone will be offered a vaccine on the NHS for free. Even if private healthcare providers order licensed vaccines we have agreed priority over delivery.”

 

Will the vaccine confer long-term immunity and stop transmission?

As trials have only been running for several months it is not possible to state the length of time for which any of the vaccine candidates will offer immunity. 


While many scientists believe that vaccination will reduce transmission as well as disease severity, to date there is a lack of substantial evidence to support this belief*. In short it is possible that vaccinated people may still be able to carry and transmit the virus. Epidemiological studies into vaccination’s impact on transmission are likely to take place alongside vaccination programmes and their findings will be key to future decisions about the loosening of restrictions in the workplace and the wider community. 


*Pfizer BioNTech and Moderna have, thus far, only reported on the ability of their candidates to prevent severe disease and the Covid-19 cases in their trials were confirmed from symptomatic infections. However, UK based participants in the Oxford trial were swabbed weekly and observed a reduction in asymptomatic infections, on which basis there is an “early indication that [the] vaccine should reduce virus transmission.”  


Implications for workplace testing: Summary


There is a high risk of post-Christmas virus outbreaks and late winter lockdowns. The initial rollout of the Pfizer vaccine will not change this and some employers are planning start term asymptomatic testing from January in order to mitigate this risk and ensure that they stay operational during the late winter months. 


UK tier restrictions and social distancing are unlikely to change before phase 1 of a vaccine rollout is complete which, even assuming the Oxford vaccine is approved, is unlikely to be before April 2021. Given the sheer numbers of people involved, it may well be later. 


The majority of private sector working-age people will not be included in either the phase 1 or phase 2 rollouts and it is unlikely that employers seeking private vaccination will be able to access this in the short term.


Most employers requiring testing to remain operational are likely to continue with their programmes until at least April, with a view to extending further into Q2 should delays in rollout occur.


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