Novavax COVID-19 vaccine
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Vaccine description | |
---|---|
Target disease | SARS-CoV-2 |
Type | Subunit |
Clinical data | |
Trade names | Covovax[1][2] |
Licence data | US Daily Med:link |
Routes of administration |
Intramuscular |
Identifiers | |
ATC code | None |
DrugBank | DB15810 |
UNII | UK9AK2IN1P |
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The Novavax COVID-19 vaccine, codenamed NVX-CoV2373, is a subunit COVID-19 vaccine candidate developed by Novavax and the Coalition for Epidemic Preparedness Innovations (CEPI), that is undergoing trials in India under the brand name Covovax.[1][6] It requires two doses[7] and is stable at 2 to 8 °C (36 to 46 °F) refrigerated temperatures.[8]
Contents
Medical uses
The vaccine is given in two doses administered 21 days apart.[9]
Efficacy
Variant | Two doses | One dose | ||
---|---|---|---|---|
Symptomatic | Hospitalization | Symptomatic | Hospitalization | |
Others circulating previously | 96% (74–99%)[lower-alpha 2] | 100%[lower-alpha 3][lower-alpha 2] | 83% (74–90%)[lower-alpha 2] | Not reported |
Alpha | 86% (71–94%)[11] | 100%[lower-alpha 3][11] | Not reported | |
Beta | 51% (−1 to 76%)[12] | Not reported | Not reported | Not reported |
Gamma | Not reported | Not reported | Not reported | Not reported |
Delta | Not reported | Not reported | Not reported | Not reported |
UK Trial
On 28 January 2021, Novavax reported that preliminary results from the United Kingdom trial showed that its vaccine candidate was more than 89% effective.[13][8] However, interim results from a trial in South Africa showed a lower effectiveness rate against the Beta variant (lineage B.1.351), at around 50–60%.[7][14]
On 12 March 2021, Novavax announced their vaccine candidate was 96.4% effective in preventing the original strain of COVID-19 and 86% effective against the Alpha variant.
On 30 June 2021, a study in the The New England Journal of Medicine funded by Novavax, showed that the vaccine had an overall efficacy of 83.4% two weeks after the first dose and 89.7% one week after the second dose. A post hoc analysis showed an efficacy of 86.3% against the B.1.1.7 (Alpha) variant and 96.4% against "non-B.1.1.7 strains" , majority of which were the "prototype strains" (original strain).[11][15]
South Africa Trial
On 28 January 2021, Novavax reported that interim results from a trial in South Africa showed a lower effectiveness rate against the Beta variant (lineage B.1.351), at around 50–60%.[7][14]
On 12 March 2021, Novavax announced their vaccine candidate proved 55% effective against the Beta variant in people without HIV/AIDS. It was also 100% effective at preventing severe illness.[16][clarification needed]
US and Mexico trial
On 14 June 2021, Novavax announced overall 90.4% efficacy in the Phase 3 U.S. & Mexico trial that involved nearly 30,000 people ages 18 years and older.[17] From the total 77 COVID-19 cases found in the trial participants, 14 occurred in the vaccine group, while 63 occurred in the placebo group.[18]
Chemistry
The formulation includes a saponin-based adjuvant.[19][20][21]
Manufacturing
NVX-CoV2373 has been described as both a protein subunit vaccine[19][20][22] and a virus-like particle vaccine,[23][24] though the producers call it a "recombinant nanoparticle vaccine".[21]
The vaccine is produced by creating an engineered baculovirus containing a gene for a modified SARS-CoV-2 spike protein. The spike protein was modified by incorporating two proline amino acids in order to stabilize the pre-fusion form of the protein; this same 2P modification is being used in several other COVID-19 vaccines.[25] The baculovirus then infects a culture of Sf9 moth cells, which create the spike protein and display it on their cell membranes. The spike proteins are then harvested and assembled onto a synthetic lipid nanoparticle about 50 nanometers across, each displaying up to 14 spike proteins.[19][20][21]
It is stable at refrigerated temperatures of 2 to 8 °C (36 to 46 °F).[8]
Novavax signed an agreement with Serum Institute of India for mass scale production for developing and low-income countries.[26] It has also been reported, that the vaccine will be manufactured in Spain[27] and in Poland by the Mabion company.[28]
On 26 May 2021, Serum Institute of India said that it has started the production of the Novavax COVID-19 vaccine candidate (branded as Covovax in India) after receiving permission from the Indian government.[29]
History
In January 2020, Novavax announced development of a vaccine candidate, codenamed NVX-CoV2373, to establish immunity to SARS-CoV-2.[30] Novavax's work is in competition for vaccine development among dozens of other companies.[31]
In March 2020, Novavax announced a collaboration with Emergent BioSolutions for preclinical and early-stage human research on the vaccine candidate.[32] Under the partnership, Emergent BioSolutions was supposed to manufacture the vaccine at large scale at their Baltimore facility.[33] However, following production issues with the Johnson & Johnson and Oxford–AstraZeneca vaccines at its Baltimore plant and to decrease the burden on the plant, Novavax subsequently partnered with a different manufacturer in a new agreement overseen by the U.S. government.[34]
Trials have also taken place in the United Kingdom.[35][36] The first human safety studies of the candidate, codenamed NVX-CoV2373, started in May 2020 in Australia.[37][38]
In July 2020, the company announced it might receive US$1.6 billion from Operation Warp Speed to expedite development of its coronavirus vaccine candidate by 2021 – if clinical trials show the vaccine to be effective.[39][40] A spokesperson for Novavax stated that the $1.6 billion was coming from a "collaboration" between the Department of Health and Human Services and Department of Defense,[39][40] where Gen. Gustave F. Perna has been selected as COO for Warp Speed. In late September, Novavax entered the final stages of testing its coronavirus vaccine in the UK. Another large trial was announced to start by October in the US.[41]
Clinical trials
In December 2020, Novavax started the PREVENT-19 (NCT04611802) phase III trial in the US and Mexico, funded by NIAID and BARDA.[42][43]
On 24 February 2021, Novavax partnered with Takeda Pharmaceutical Company in Japan, where its COVID-19 vaccine candidate is known as TAK-019.[44]
On 3 May 2021, Novavax initiated a pediatric expansion for the phase 3 clinical trial, with 3,000 adolescents 12–17 years old.[45]
Authorizations
In February 2021, the European Medicines Agency (EMA) started a rolling review of the Novavax COVID-19 vaccine (NVX‑CoV2373).[3]
Society and culture
Economics
On 2 February 2021, Canadian Prime Minister Justin Trudeau announced that Canada has signed a tentative agreement for Novavax to produce millions of doses of its COVID-19 vaccine at a National Research Council facility in Montreal once it is approved for use by Health Canada, making it the first COVID-19 vaccine to be produced domestically in that country.[46] During the initial vaccination stages of the COVID-19 pandemic Canada's program was hampered due to relying solely on vaccines imported from Europe, India, and later the United States.
On 16 March 2021, Philippine vaccine czar Carlito Galvez Jr. announced a purchase agreement for the Novavax vaccine of 30 million doses for the national vaccination program that shall be produced by the Serum Institute of India, being the first Southeast Asian country to procure the said vaccine.[47]
On 29 March 2021, the UK government announced that their order for 60 million doses of the Novavax vaccine, which will be manufactured in the UK by FUJIFILM Diosynth Biotechnologies, will also be filled and finished in the UK by GlaxoSmithKline.[48]
On 24 June 2021, Singapore's Health Minister Ong Ye Kung announced an advance purchase agreement signed for supplies of Novavax vaccine with promising results shown, which will arrive by end-2021.[49]
Notes
- ↑ A vaccine is generally considered effective if the estimate is ≥50% with a >30% lower limit of the 95% confidence interval.[10]
- ↑ 2.0 2.1 2.2 28 September 2020 to January 2021, United Kingdom.[11] According to Nextstrain, during this period, the Alpha variant completely replaced the previously dominant lineage B.1.282 by the end of October.
- ↑ 3.0 3.1 No cases detected.
References
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- ↑ Clinical trial number NCT04611802 for "A Study Looking at the Efficacy, Immune Response, and Safety of a COVID-19 Vaccine in Adults at Risk for SARS-CoV-2" at ClinicalTrials.gov
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