‘Enhanced immunity, no
serious adverse events’: Lancet releases Covaxin’s Phase 1 trial data
At a time when coronavirus vaccines are being
administered in various parts of the country, there is also a steep rise in
concerns regarding the side effects of the vax shot. But, there is a good news.
Phase 1 trial report of India’s first indigenous vaccine against COVID-19,
Covaxin, showed enhanced immune response without any serious side effects in
the participants.
Covaxin Was Given The Emergency Authorisation By The
Indian Government
The Indian government had given Covaxin emergency use
authorisation in clinical trial mode. The vaccine was developed by Bharat
Biotech in collaboration with the Indian Council of Medical Research (ICMR) and
the National Institute of Virology (NIV), Pune.
Covaxin, which is currently undergoing phase-3 trials,
had raised concerns among experts over its emergency approval earlier this
month by India’s drug regulator.
The vaccine, codenamed BBV152, was well tolerated in
all dose groups with no vaccine-related serious adverse events, noted the authors of the study funded by
Bharat Biotech.
Reported Adverse Events Are Mild And Moderate
According to the authors all adverse events were mild
and moderate, and were more frequent after the first dose, adding that one
adverse event was reported but was unrelated to the vaccine.
The randomised phase 1 trial to assess the safety
and immunogenicity of BBV152 was carried at 11 hospitals
across India.
Adults aged 18-55 years who were deemed healthy by the
investigator were eligible. Between July 13 and 30, last year, 827 participants
were screened, of whom 375 were enrolled.
Among the enrolled participants, 100 each were
randomly assigned to the three vaccine groups, and 75 were randomly assigned to
the control group.
The Doses Of Covaxin And The Mild Adverse Events You
Can Expect
Two intramuscular doses of vaccines were administered
14 days apart. “BBV152 led to tolerable safety outcomes and enhanced immune
responses. The vaccine was well tolerated in all dose groups with no
vaccine-related serious adverse events,” the authors of the study said.
So there will be mild adverse events… what are those?
According to the experts, the most common adverse event was pain at the
injection site, followed by headache, fatigue, and fever.
Covaxin is an inactivated vaccine developed by
chemically treating novel coronavirus samples to make them incapable of
reproduction.
This process leaves the viral proteins, including
the spike protein of the coronavirus which it uses to enter
the human cells, intact.
Given as two doses, three weeks apart, the viral
proteins in the vaccine activate the immune system and prepare people for
future infections with the actual infectious virus.
According to Bharat Biotech, the therapeutic can be
stored at room temperature for at least a week.
Source: https://www.thehealthsite.com/news
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