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Covid-19: Zydus seeks DCGI approval to undertake clinical trials for antibody cocktail

It is the only Indian company to have developed a neutralizing monoclonal antibody-based cocktail for the treatment of Covid-19

Published on: May 27, 2021, 11:47:16 IST
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Pharmaceutical major Zydus Cadila has sought national drugs controller’s permission to initiate phase 1/3 human clinical trials for its monoclonal antibodies to treat Coronavirus disease (Covid-19), the company announced on Thursday.

Representational Image. (File photo)
Representational Image. (File photo)

It is the only Indian company to have developed a neutralizing monoclonal antibody-based cocktail for the treatment of Covid-19.

“At this juncture, there is a critical need to explore safer and more efficacious treatments to combat Covid. It is important to look at different stages of the disease progression and look at options that can reduce a patient’s suffering and discomfort. We believe that ZRC-3308 has the potential to address these concerns and provide a safe treatment,” said Sharvil Patel, managing director, Cadila Healthcare Ltd.

Monoclonal antibodies are laboratory-made proteins that mimic the immune system’s ability to fight off harmful pathogens such as viruses.

It’s biological therapy, ZRC-3308, is a cocktail of two SARS-CoV-2-neutralizing monoclonal antibodies (mAbs) that the company says can emerge as one of the main treatments for mild Covid-19 because they significantly reduced viral load in mild patients and their rate of hospitalisation.

According to the company, the monoclonal antibodies of ZRC-3308 have been specifically designed to provide protection for a much longer period of time than the currently approved products.

“The enhanced design would also help in preventing any further tissue damage, thereby reducing the risk of severe disease. ZRC-3308 has demonstrated the ability to neutralise SARS-CoV-2 both in vitro and in animal studies,” said the company in a statement.

“In animal studies, ZRC-3308 reduced damage to the lungs in both prophylactic and therapeutic settings. It has been found to be safe and well tolerated in animal toxicology studies. Zydus is currently seeking permission to initiate phase 1/3 human clinical trials from the drugs controller General of India.”

This Monday, Roche India had launched its monoclonal antibodies for Covid-19 treatment in Indian market.

 
ABOUT THE AUTHOR
Rhythma Kaul

Rhythma Kaul is the national health editor of the Hindustan Times. She has been reporting on public health, medicine, and medical research, with a particular focus on how government decisions and health system reforms shape people’s lives. Rhythma has over 25 years of journalistic experience. She joined Hindustan Times in 2008, and has since covered everything from pandemics and infectious diseases to cutting‑edge medical research and climate‑related health challenges. Her stories routinely track the work of the Ministry of Health and Family Welfare, department of pharmaceuticals, and key national health programmes, making complex medical science and policy accessible to a wide audience. One of her prominent news breaks has been the 2012 Baby Falak case: A two-year-old brutally battered baby girl was admitted to AIIMS-Delhi with severe head injuries, multiple fractures, human bite marks, and burns. The police investigation revealed this to be a case of multi-state human-trafficking racket. She was profiled by The Wall Street Journal for breaking this story. Rhythma holds a Master’s degree from Jawaharlal Nehru University, Delhi. Prior to Hindustan Times, she worked with the India Today Group. Rhythma can be contacted at rhythma.kaul@hindustantimes.com. Her X handle is @RamblingBrook.

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