Close
CDMO Safety Testing 2026
Novotech

Oxford University resume Covid-19 vaccine trial

Note* - All images used are for editorial and illustrative purposes only and may not originate from the original news provider or associated company.

Subscribe

- Never miss a story with notifications

- Gain full access to our premium content

- Browse free from any location or device.

Media Packs

Expand Your Reach With Our Customized Solutions Empowering Your Campaigns To Maximize Your Reach & Drive Real Results!

โ€“ Access the Media Pack Now

โ€“ Book a Conference Call

โ€“ Leave Message for Us to Get Back

Related stories

BeOne Signs $2B Trispecific Antibody Deal with Huahui Health

BeOne Medicines has entered into a high-value agreement with...

Glass vs Polymer: Choosing the Right Material for Parenteral Packaging

In the pharmaceutical industry, material selection plays a critical...
- Advertisement -

Oxford University on Saturday, 13th Sep. 2020 announced resuming coronavirus vaccine trials, the study which was suspended following a reported side-effect in a UK patient. Oxford University, developing this vaccine with pharmaceutical company AstraZeneca confirmed the restart across all of its UK clinical trial sites after regulators gave the go-ahead following the pause on Sunday, 6th Sep. 2020.

โ€œThe independent review process has concluded and following the recommendations of both the independent safety review committee and the UK regulator, the MHRA, the trials will recommence in the UK,โ€ it said.

With around 18,000 people received it’s vaccine so far and around 30,000 volunteers being recruited in the US, their vaccine stands as a strongest contenders among the dozens of Covid-19 vaccines in various stages of testing around the world. The restart was also welcomed by British health secretary Matt Hancock, stating in a tweet that it was โ€œgood news for everyoneโ€ and that the trial is โ€œback up and runningโ€. The university said in large trials such as this โ€œit is expected that some participants will become unwell and every case must be carefully evaluated to ensure careful assessment of safetyโ€.

Latest stories

Related stories

BeOne Signs $2B Trispecific Antibody Deal with Huahui Health

BeOne Medicines has entered into a high-value agreement with...

Glass vs Polymer: Choosing the Right Material for Parenteral Packaging

In the pharmaceutical industry, material selection plays a critical...

FDA Advances Real-Time Clinical Trials With AstraZeneca, Amgen

The U.S. Food and Drug Administration has unveiled a...

Subscribe

- Never miss a story with notifications

- Gain full access to our premium content

- Browse free from any location or device.

Media Packs

Expand Your Reach With Our Customized Solutions Empowering Your Campaigns To Maximize Your Reach & Drive Real Results!

โ€“ Access theMedia Pack Now

โ€“ Book a Conference Call

โ€“ Leave Message for Us to Get Back

Translate ยป