Central Drug Authority approves two more US-based vaccines for India


Two more US-based COVID vaccines have been approved by the Central Drug Authority this week for use in India, boosting the arsenal to vaccinate the deeper population of the country faster.

India’s Ambassador to the US, Taranjit Singh Sandhu, was happy to announce the news and praise the great collaboration of the India-US healthcare model.

“Models of what India-United States healthcare collaboration can achieve for global good!” Sandhu said.

Indian companies working with Texas Children’s, Baylor College of Medicine’s National School of Tropical Medicine; Dr. Peter Hotez, Prof and Dean of the National School of Tropical Medicine at Baylor and Co

Director of the Texas Children’s Hospital Center for Vaccine Development; NovaVax; Merck and Ridgeback Bio, tweeted the Indian diplomat.

During his visit to Houston in October, Sandhu had met Professor Hotez and held discussions on this issue.

In June this year, the ambassador visited the Novavax facility in Maryland. He also spoke to the CEO of Sanisure Thomas Hook.

Sanisure supplies components for the SII – Novavax collaboration. These have been part of a continuous outreach that the ambassador had with vaccine manufacturers and pharma companies.

Corbevax, a protein sub-unit Covid-19 vaccine, whose technology was created and engineered in collaboration with Texas Children’s Hospital and Baylor College of Medicine has received Emergency Use Authorization (EUA) approval from the Drugs Controller General of India (DCGI). The vaccine is being launched in India with other underserved countries to follow, Texas Children’s Hospital said in a statement.

“This announcement is an important first step in vaccinating the world and halting the pandemic. Our vaccine technology offers a path to address an unfolding humanitarian crisis, namely the vulnerability the low- and middle-income countries face against the delta variant,” Hotez said.

“Widespread and global vaccination with our Texas Children’s-Baylor-BE vaccine would also forestall the emergence of new variants. We have previously missed that opportunity for the alpha and delta variant. Now is our chance to prevent a new global wave from what might follow,” he said.

Dubbed “the world’s Covid-19 vaccine”, it uses a traditional recombinant protein-based technology that will enable its production at large scales making it widely accessible to inoculate the global population, the statement said.

Corbevax after completing two Phase III clinical trials involving more than 3,000 subjects was found to be safe, well-tolerated and immunogenic. It demonstrated superior immune response in comparison with the Covishield vaccine when assessed for Neutralising Antibody (nAb) Geometric Mean Titers (GMT) against the Ancestral-Wuhan strain and the globally dominant Delta variant.