BENGALURU (Reuters) -The Indian drug regulator’s subject expert committee has recommended emergency use approval for Zydus Cadila’s three-dose COVID-19 vaccine, CNBC-TV18 reported https://twitter.com/CNBCTV18Live/status/1428622962400264200 on Friday, citing sources.
The committee added that Zydus needs to submit additional data for the 2-dose regimen of its vaccine, CNBC-TV18 said in a tweet.
The generic drugmaker, listed as Cadila Healthcare Ltd, applied for the authorisation of the vaccine ZyCoV-D on July 1, based on an efficacy rate of 66.6% in a late-stage trial of more than 28,000 volunteers nationwide.
If approved, Zydus Cadila’s vaccine will be the second home-grown shot to get emergency authorisation in India after Bharat Biotech’s Covaxin.
Zydus Cadila and India’s drug regulator did not immediately respond to a Reuters request for comment.
(Reporting by Shivani Singh in Bengaluru; Editing by Ramakrishnan M.)
