DUBAI (Reuters) - An experimental coronavirus vaccine developed by China National Pharmaceutical Group (Sinopharm) has 86% efficacy, the health ministry of the United Arab Emirates said on Wednesday, citing an interim analysis of late-stage clinical trials.
While the positive data comes soon after last month's upbeat results from Western rivals, such as Pfizer Inc, Moderna, AstraZeneca Plc and from Russia, neither the UAE nor Sinopharm have released detailed data from the pivotal study.
In July, the Gulf Arab state started Phase III clinical trials of the vaccine, developed by Beijing Institute of Biological Product, a unit of Sinopharm's China National Biotec Group (CNBG).
In September, it authorised emergency use of the vaccine for certain groups, the first such international clearance for a vaccine developed in China.
The analysis also shows "99% seroconversion rate of neutralizing antibody and 100% effectiveness in preventing moderate and severe cases of the disease", the ministry said in a statement carried by the state news agency.
"The analysis shows no serious safety concerns," it said.
It also said it had officially registered the vaccine, without elaborating, and that 31,000 volunteers across 125 nationalities participated in the UAE trial.
It did not say what, if any, side effects it identified, how many participants have become ill or how many volunteers were given the vaccine or a placebo.
CNBG could not be immediately reached for comment.
The vaccine, which uses an inactivated virus unable to replicate human cells to trigger immune responses, requires two doses, past trial data has showed.
The UAE trial is a partnership between CNBG, Abu Dhabi-based artificial intelligence company Group 42 (G42) and the Abu Dhabi Department of Health.
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