COVID-19 Vaccine Update: Hyderabad-Based Biological E Begins Clinical Trials of Coronavirus Vax
Biological E. Ltd (BE), a Hyderabad-based vaccines and pharmaceutical company, on Monday announced that it has initiated clinical trial of its Covid-19 subunit vaccine candidate in the country following approval from the Drugs Controller General of India (DGCI).
Hyderabad, November 16: Biological E. Ltd (BE), a Hyderabad-based vaccines and pharmaceutical company, on Monday announced that it has initiated clinical trial of its Covid-19 subunit vaccine candidate in the country following approval from the Drugs Controller General of India (DGCI). BE is making the vaccine in collaboration with Dynavax Technologies Corporation (Dynavax), a US-based vaccine focused biopharmaceutical company, and Baylor College of Medicine, a health sciences university in Houston.
The vaccine candidate includes an antigen in-licensed from BCM Ventures, Baylor College of Medicine's integrated commercialisation team, along with Dynavax's advanced adjuvant CpG 1018, BE said in a statement. BE's Phase 1/2 clinical trials will evaluate the safety and immunogenicity of the vaccine candidate consisting of the receptor binding domain of the spike protein of SARS-CoV-2 at three dose levels adjuvanted with CpG 1018 plus alum, in about 360 healthy subjects in the age range of 18 to 65 years, it said. COVID-19 Vaccine in India Update: Vaccinating 130 Crore People With Injectable Covaxin a Challenge, Says Bharat Biotech.
The vaccination schedule consists of two doses for each study participant, administered via intramuscular injection 28 days apart. The results of this clinical trial are expected to be available by February 2021. "The transition of our vaccine candidate into human trials is an important milestone, and exemplifies a successful transfer of technology with BE, that could lead to a safe, effective and affordable vaccine," said Dr Maria Elena Bottazzi, associate dean of the National School of Tropical Medicine at Baylor College of Medicine and co-director of Texas Children's Hospital Center for Vaccine Development. COVID-19 Vaccine Covishield May Get Emergency Use Authorisation From India in December 2020, Says Report.
"This vaccine represents an urgent biotechnology innovation for ensuring health equity and combating the Covid-19 pandemic," said Dr. Peter Hotez, professor and dean of the National School of Tropical Medicine at Baylor and co-director of Texas Children's Hospital Center for Vaccine Development. "We are very happy indeed to transition our potential vaccine candidate to clinical trials and offer one more potential option for the prophylaxis of Covid-19," said Mahima Datla, Managing Director, Biological E. Ltd.
"We are proud to contribute CpG 1018 to support development of an adjuvanted vaccine to prevent Covid-19. CpG 1018's potential to boost the immune response to produce more antibodies and longer lasting immunity may also minimise the dose of antigen needed, enabling vaccination of a greater number of people," said Ryan Spencer, Chief Executive Officer of Dynavax.
(The above story first appeared on LatestLY on Nov 16, 2020 05:17 PM IST. For more news and updates on politics, world, sports, entertainment and lifestyle, log on to our website latestly.com).