Chandigarh based the Post Graduate Institute of Medical Education and Research (PGIMER) has administered the first dose of Oxford Covid-19 vaccine — Covishield — to three candidates on Friday, PGI Chandigarh Director Jagat Ram said.

The clinical trials of Oxford vaccine has started at PGI Chandigarh after the institute administered first dosage of the vaccine to three volunteers on Friday, Jagat Ram said.

Ram said that two females and a male were given dosage of 0.5 ml.

“Two females aged 57 and 26 years and a 33-year-old male were administered the vaccine candidate at the institute,” he added.

The PGIMER is one of the seventeen sites where phase II trials of the ‘Covishield’ vaccine developed by Oxford University and being mass-produced by Pune based Serum Institute of India (SII) is being conducted.

A source privy to the development confirmed that the candidates will be monitored for 28 days after the 0.5 ml dose of vaccine and then the second dose will be given followed by a monitoring of 28 days.

After that a blood sample will be taken and they will be observed for a span of six months.

Besides, the candidates have been asked to note any development of symptoms like fever in their personal diary.

18 candidates have been found eligible till now to undergo the trial.

The institute plans to take 100 candidates into the phase II study while it has made commitment for 253 candidates to Indian Council of Medical Research (ICMR).

The trials started after the institute received safety approval pending from the Data Safety and Monitoring Board (DSMB) for the first 100 candidates selected to undergo the trials last week.

The institute had earlier claimed to start the trials by the first week of September.

However, it was initially delayed due to pending safety approvals of the candidates from DSMB.

Later, the trials were suspended pan-India by Central Drugs Standard Control Organisation (CDSCO) after COVID-19 vaccine trials were put on hold in the United Kingdom (UK) as one of the participants there reported a severe adverse reaction following administration of a booster dose.

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