CanSino Phase 3 Covid-19 vaccine trial expected to begin this month

ISLAMABAD: Falling Covid-19 infection numbers in Pakistan will not affect a Phase 3 clinical trial for a potential vaccine being developed by China's CanSino Biologics, which is expected to begin this month, according to officials running the trial.

Pakistan's drug regulator last month gave the go-ahead for the country's first Phase 3 clinical trial for CanSino's candidate, Ad5-nCoV, which will be led by the government-run National Institute of Health (NIH) along with pharmaceutical company AJM - the local representative of CanSino.

"We are planning to launch the project on September 20, or at the latest within this month," Hassan Abbas Zaheer, who is heading the trial for AJM, told Reuters.

The Ad5-nCoV vaccine and placebo injections are due to be received in Pakistan next week.

Daily positive cases in Pakistan peaked at more than 6,000 in June, but have since fallen sharply, with only 426 confirmed new cases detected on September 8 - taking its total to 299,659 and 6,359 deaths.

Zaheer said the low positive rates did not indicate COVID-19 was no longer present in the country, and the potential for people vaccinated in the trial to be infected was still adequate for testing their immunity.

"We feel people are still getting infected but not getting tested, so the virus is still there," he said.

Pakistan, a country of more than 220 million people, has been testing between 20,000 to 30,000 daily.

Aamer Ikram, Executive Director of the NIH, told Reuters that officials believed the prevalence of the virus in Pakistan was low, despite the low testing rate, but researchers had a plan in place for the trial.

"We have been strategizing with CanSino on how to make sure people who are more exposed to the virus are recruited for volunteers, so we will be targeting front-line workers who have more chances of exposure."

The Ad5-nCoV trial will recruit around 8,000 volunteers, most of whom will be health workers. They will be recruited over a four-month period and be followed for 12 months after receiving the vaccine or placebo.