Vaccine description | |
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Target | SARS-CoV-2 |
Vaccine type | Viral vector |
Clinical data | |
Trade names | Convidecia |
Other names | PakVac |
Routes of administration | Intramuscular, Nebulizer |
ATC code | |
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COVID-19 pandemic |
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COVID-19 portal |
AD5-nCOV, trade-named Convidecia, is a single-dose[2] viral vector vaccine for COVID-19 that is also used as an inhaled booster. It was developed by CanSino Biologics, with Phase III trials conducted in Argentina,[3] Chile,[4] Mexico,[5] Pakistan,[6] Russia,[7] and Saudi Arabia[8] with 40,000 participants.
In February 2021, global data from Phase III trials and 101 COVID cases showed that the intramuscular version of the vaccine had a 65.7% efficacy in preventing moderate symptoms of COVID-19, and 91% efficacy in preventing severe disease.[9] It has similar efficacy to the Janssen vaccine, another one-shot adenovirus vector vaccine with 66% efficacy in a global trial.[10][2] Convidecia is similar to other viral vector vaccines like AZD1222, Gam-COVID-Vac, and Ad26.COV2.S.[11] Its single-dose regimen and normal refrigerator storage requirement (2° to 8 °C) could make it a favorable vaccine option for many countries.[10] It is currently under evaluation for emergency use listing by the WHO.[12] On May 19 2022, WHO issued EUL for the vaccine.[13]
A Phase I study published in The Lancet showed two doses of a nebulised version of Convidecia (inhaled through the mouth) resulted in neutralising antibody responses similar to the existing one-dose injection.[14]
Convidecia and the Pakistani version called PakVac are approved for use by some countries in Asia,[15][16][17] Europe,[18][19] and Latin America.[20][21][22] Production capacity for Ad5-NCov should reach 500 million doses in 2021. Manufacturing will take place in China,[23] with filling and finishing of the vaccine additionally also taking place in Malaysia,[17] Mexico,[24] and Pakistan.[25]
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