Texas Children’s Hospital and Baylor College of Medicine today announced Corbevax — a protein sub-unit COVID-19 vaccine — has received approval from the Drugs Controller General of India to launch in that nation.
The vaccine has been developed in Houston by Dr. Peter Hotez, the dean of the National School of Tropical Medicine at Baylor College of Medicine and co-director of the Center for Vaccine Development at Texas Children’s Hospital and Dr. Maria Elena Bottazzi.
Hotez called the approval “an important first step in vaccinating the world and halting the pandemic.”
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Bottazzi and Hotez led efforts at Texas Children’s Hospital to develop the “initial construct and production process of the vaccine antigen.” After the vaccine was found to be “safe, well tolerated and immunogenic,” the Drugs Controller General of India granted emergency use authorization.
Corbevax completed two Phase III clinical trials with more than 3,000 subjects. The trials suggested a better immune response to the Ancestral-Wuhan strain of the virus as well as the delta variant compared to Covishield, which was developed by Oxford-AstraZeneca. None of the subjects showed severe adverse reactions to the vaccine; and adverse effects in the study were half of those from Covishield.
See here for the background. Vaccine supply isn’t a problem in the US and Europe but it is a problem in many parts of the world. We know very well that the more opportunities this virus gets to spread and mutate, the more chances it has to turn into something worse and more dangerous. Hopefully Corbevax can help close that gap. Kudos to all involved. Here’s the Texas Children’s Hospital page about Corbevax and its development, and CultureMap has more.