DCGI panel to hold discussion on intranasal "Five Arms" booster dose iNCOVACC on Nov 15: Sources
It has now announced that iNCOVACC (BBV154) has received approval under Restricted Use in Emergency Situation for ages 18 and above.;
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New Delhi: The Subject Expert Committee (SEC) members of the Drugs Controller General of India (DCGI) are going to meet on November 15 and hold a discussion on intranasal "Five Arms" booster dose - iNCOVACC (BBV154), official sources told the media agency.
"Developed by the Bharat Biotech International Limited (BBIL), the five arms heterologous intranasal booster dose means, "Arm 1: 2 covaxin - booster covaxin, Arm 2: 2 covaxin - booster I/N vaccine, Arm 3: 2 Covishield- booster Covishield, Arm 4: 2 Covishield- booster I/N vaccine, Arm 5: 2 intranasal- booster intranasal," they explained.
DCGI has already given emergency use authorization (EUA) to BBIL for the intranasal vaccine.
BBIL had in September this year, applied for DCGI's approval for market authorization of its "Five Arms" intranasal heterologous booster dose. It has now been announced that iNCOVACC (BBV154) has received approval under Restricted Use in Emergency Situation for ages 18 and above.
"We are proud to announce the approval of iNCOVACC, a global game changer in Intra Nasal vaccines technology and delivery systems. Despite the lack of demand for COVID-19 vaccines, we continued product development in intranasal vaccines to ensure that we are well-prepared with platform technologies for future infectious diseases. We thank the Ministry of Health, the CDSCO, the Dept of Biotechnology Govt of India, and Washington University St. Louis for their support and guidance. iNCOVACC has been designed for efficient distribution and easy administration," BBIL's Chairman and Managing Director, Dr Krishna Ella, had said in a statement.
Read also: Bharat Biotech Covaxin 50 million doses set to expire early 2023 due to poor demand
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