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After obtaining the requisite clearance from the Central Drugs Laboratory, Dr. Reddy's Laboratories and RDIF have begun adaptive phase 2/3 clinical trials for the Sputnik V vaccine in India. The trial is a multicenter and randomised controlled safety and immunogenicity study.
Gemcovac-19 is the first approved mRNA based Covid-19 vaccine developed with the use of genetically engineered mRNA which instructs the cells to make the S-protein found on the surface of the Covid-19 virus, causing the body to create antibodies.
Company has conducted phase-2/3 trials of vaccine candidates to evaluate its safety, immunogenicity and tolerability on 4,000 participants, for first indigenously developed HGCO19, mRNA vaccine for Covid-19.
Gennova's synthetic, self-replicating India's first homegrown mRNA vaccine is in Phase III Clinical Trials for the treatment of COVID-19 is currently under final clinical trial stages.
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Corbevax is in phase-3 trials and likely to complete all the studies by end of November which is when company is expecting licence. The licence for children should follow one month later.
Corbevax is an RBD protein based sub-unit vaccine against the coronavirus infections. Corbevax is based on a protein antigen technology that binds to the Angiotensin Converting Enzyme-2 (ACE2) receptor on the host cell membrane.
Currently, phase 2/3 clinical trials of the second indigenously developed Corbevax, an RBD protein sub-unit vaccine to be administered in adults aged 18 years to 80 years, is underway and the results are likely to be declared this month.
Corbevax is an RBD protein sub-unit vaccine that has been developed with supported from the Department of Biotechnology and its PSU Biotechnology Industry Research Assistance Council (BIRAC).
BBIL’s BBV87 vaccine is an inactivated whole virion vaccine based on strain derived from an East, Central, South African (ECSA) genotype. IVI is advancing clinical development of BBV87 to evaluate safety and immunogenicity of 2-dose regimen of BBV87 Chikungunya vaccine.
Phase 1 trial of the adenoviral intranasal vaccine, BBV154 in healthy volunteers of age groups ranging from 18 to 60 years was well tolerated, the science and technology ministry said in a release on Friday.