Good news! UK adds India-made Covaxin to its list of approved COVID-19 vaccines

India's indigenously-made 'Covaxin', one of the vaccines being used nationwide in the inoculation campaign against the COVID-19 pandemic, is on the UK's list of approved COVID-19 vaccines for international travellers from Monday.

It will benefit more fully vaccinated Indians planning travel to the UK without the need for a pre-departure PCR test or self-isolation at the address declared on their compulsory Passenger Locator Forms.

Like other fully vaccinated travellers, including those vaccinated with Covishield, they are required to pre-book a PCR or Lateral Flow Test on arrival in England, to be taken before the end of day 2.

"From 4am on Monday 22 November, the government will recognise vaccines on the World Health Organisation's Emergency Use Listing (WHO EUL) at the border," the UK's Department for Transport (DfT) confirmed.

"As a result, Sinovac, Sinopharm Beijing and Covaxin will be added to our existing list of approved vaccines for inbound travel, benefitting more fully vaccinated passengers," it said.

Earlier this month, the Bharat Biotech manufactured Covaxin - the second most used formulation in India - had received its WHO EUL status, resulting in the UK announcing plans to include it on its list of approved COVID vaccines from November 22.

The WHO Emergency Use Listing process includes a review of the quality, safety and efficacy data performed by WHO experts and many countries such as the United States, Spain, Sweden, Switzerland and Iceland recognise this categorisation.

Meanwhile, travellers who aren't fully vaccinated against COVID-19 are required to undergo a pre-departure test and 10-day quarantine at a declared address in Britain.

From Monday, the UK government said it is also simplifying travel rules for all under-18s coming to England from a non-red-list country, who will be treated as fully vaccinated at the border, regardless of their individual vaccination status.

For those who want to know about India’s Covaxin,

Here are some Q&A.

https://www.bmj.com/content/373/bmj.n997

Q: Who developed Covaxin?

Covaxin was developed by Indian pharmaceutical company Bharat Biotech in collaboration with the Indian Council of Medical Research, a government funded biomedical research institute, and its subsidiary the National Institute of Virology.

Bharat Biotech has brought to market 16 original vaccines, including for rotavirus, hepatitis B, Zika virus, and chikungunya.1 The company reportedly spent $60-$70m (£43-£50m; €50-€58m) developing Covaxin.

Q: How does Covaxin work?

The vaccine is similar to CoronaVac (the Chinese vaccine developed by Sinovac) in that it uses a complete infective SARS-CoV-2 viral particle consisting of RNA surrounded by a protein shell, but modified so that it cannot replicate.4

Covaxin comes as a two-dose regimen, recommended to be taken 28 days apart.

Q: What peer reviewed data are available for the vaccine?

Covaxin’s phase I trial to assess safety and immunogenicity is published.5 All 375 subjects who received the vaccine had notably elevated antibody response.

The phase II trial result has not yet been published in a peer reviewed journal, but a preprint has been posted on MedRxiv.7 The provisional data indicate enhanced immune response and tolerable safety outcomes.

Since November, 25 800 participants have been enrolled in ongoing phase III trials. Bharat Biotech released interim efficacy data on 3 March 2021, which showed a clinical efficacy of 81%.

Q: Why did India choose to develop its own vaccine?

With the goal of vaccinating 300 million people every quarter, costs are mounting. Doctors say it may take two years to vaccinate the entire population.9 The first round of immunisations has been subsidised by the government and is free for India’s 30 million health workers, older people, and frontline workers.

Each dose of Covaxin costs 295 rupees (£2.93 versus £19-£28 for the Moderna vaccine11 and £26.70 for the Pfizer/BioNTech12). Moreover, Bharat Biotech is providing the first 1.65 million doses at no cost to the government. This makes the Indian vaccine the cheapest purchased by any country in the world at 206 rupees per shot for the 5.5 million doses the government currently has on order. The government has capped the price of the vaccine sold in the private market, with private hospitals able to charge up to 250 rupees.

Covaxin does not require storage at sub-zero temperatures, which would be hard to maintain in India’s climate and with the frequent power cuts in rural areas. Covaxin is available in multi-dose vials and is stable at the 2-8°C that ordinary refrigeration can achieve.

Bharat Biotech says it has a stockpile of 20 million doses of Covaxin for India and is in the process of manufacturing 700 million doses at its four facilities in two cities by the end of the year. It says it can provide 300 million shots annually.

Q: When was Covaxin approved for public use?

The Central Drugs and Standards Committee (CDSCO), India’s top drug regulator, issued an emergency approval for Covaxin on 3 January 2021, even though phase III clinical trials are still ongoing and phase II studies are unpublished.14 The regulator cited the need for protection against the potential spread of the UK variant. No peer reviewed evidence is available to show that the vaccine would be effective against this strain, although a preprint indicates promising results.

The vaccine is currently being administered in India to people over 60 and those over 45 with comorbidities, as well as to health workers. At the time of writing, India had administered more than 100 million vaccinations, although it is not clear how many are Covaxin (most are Covishield, India’s version of the Oxford-AstraZeneca vaccine manufactured in Pune by the Serum Institute of India).

Q: Which other countries have ordered Covaxin?

Bharat Biotech has signed deals with Ocugen, a US based biopharmaceutical company, to produce the vaccine for the US market, and Precisa Medicamentos to supply to Brazil, pending regulatory approval there.

How has Covaxin been received by the medical community?
The emergency approval before phase III trials were completed triggered widespread criticism from the scientific community in India.

With nearly 14 million coronavirus infections at the time of writing, India has the second highest number of reported cases globally after the US, but the approval came at a time when cases were dropping.

The CDSCO said the vaccine had been approved for “restricted use in an emergency situation” and that it would be deployed in a “clinical trial mode.” This vague terminology, with no official clarification, has left doctors and scientists puzzled, though one doctor The BMJ spoke to said it implied that safety data would be collected.

The All India People’s Science Network, which represents numerous scientific organisations, described the approval of Covaxin as “hasty,” while the All India Drug Action Network, a group of non-government organisations working to increase access to essential medicines, said it was “shocked” and “baffled” by the decision. In the interest of “public welfare and transparency” the group urged regulators to make the data public.

To compound this anxiety, one participant in the phase III trials died. The hospital at which the trial took place, the People’s College of Medical Sciences and Research Centre in Bhopal, has been accused of not following proper procedures while screening candidates for the trials.

However, 45 doctors—including two former directors of the All India Institute of Medical Science—labelled the criticisms of Covaxin as “irresponsible.”17 They called the vaccine India’s “gift to humanity.”

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