DCGI gives nod for Vaccine’s phase-II/III trials on kids aged between 5 and 18

The DCGI’s permission was given based on the recommendations by the Subject Expert Committee (SEC) on C-19.


Last Updated on September 4, 2021 by The Health Master

The Drugs Controller General of India (DCGI) yesterday granted permission to Hyderabad-based Biological E to conduct phase-II/III clinical trials of its ‘Made in India’ C-19 vaccine on children aged between five and 18 years with certain conditions, sources said.

The phase-II and -III clinical trials have to be conducted as per approved protocol titled ‘A Prospective, Randomised, Double-blind, Placebo-controlled, Phase-II/III Study to Evaluate Safety, Reactogenicity, Tolerability and Immunogenicity of Corbevax Vaccine in Children and Adolescents,’ a source said.

The DCGI’s permission was given based on the recommendations by the Subject Expert Committee (SEC) on C-19.

So far, indigenously developed Zydus Cadila’s needle-free C-19 vaccine ZyCoV-D has received Emergency Use Authorisation from the drug regulator, making it the first vaccine to be administered in the age group of 12-18 years in the country.

Picture: Pixabay

Meanwhile, the data of phase-II/III clinical trials of Bharat Biotech’s Covaxin in the age group two-to-18 years is underway.

India’s drug regulator in July granted permission to the Serum Institute of India (SII) for conducting phase-II/III trials of Covovax on children aged two-to-17 years with certain conditions.

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Biological E’s anti-coronavirus shot, Corbevax, which is an RBD protein sub-unit vaccine, is currently undergoing phase-II/III clinical trials on adults, sources had said earlier.

Biological E will supply 30 crore doses of Corbevax to the central government by December, as announced by the Union Health Ministry in June. The ministry finalised arrangements with the Hyderabad-based vaccine manufacturer to reserve 30 crore vaccine doses, an official statement had said.

The Biological E C-19 vaccine candidate has been supported by the Government of India from the pre-clinical stage to the phase-III studies. The Department of Biotechnology (DBT) has not only provided financial assistance in terms of grant-in-aid of over Rs 100 crores, but has also partnered with Biological E to conduct all animal challenge and assay studies through its Research Institute Translational Health Science Technology Institute (THSTI), Faridabad, a Health Ministry statement had stated.

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