Carian mengenai topik US FDA

It needed more data from an ongoing trial of a third vaccine dose in younger children in order to move forward with emergency use authorisation.

Many scientists tracking the data believe it's the right time for the move.

The US FDA authorisation of the vaccine for kids aged five to 11 paves the way for the innoculation of 28 million children in the US.

The panel's vote is an important regulatory step in getting the vaccine into the arms of millions of children.

Biogen said the main goal of the current study will be to evaluate how well Aduhelm slows the progress of Alzheimer's in dosed patients.

The objective of the discussion with the US FDA is to enroll a larger safety database, which increases the likelihood of detecting rarer events.

Our actions in the next few months will shape Malaysia's trajectory towards recovery.

A rundown of the most important stories you need to know for the day, from the newsroom of Astro AWANI.

The US agency will analyze data from clinical trials of several vaccines using these viral vectors to look for clues.

The FDA stopped short of committing to issuing new regulations, however.

There is also concern that longer gaps between doses could provide the ideal environment for the virus to mutate further.

Scientists must agree upon at what point a variant has strayed too far from the unaltered virus and requires a new vaccine.

Healthcare workers and elderly people are expected to be the main recipients of a first round of 2.9 million doses.

Some want more time, despite assurances from experts that they trust the vaccine vetting process carried out by the US FDA.

The US FDA will immediately begin evaluating the results of the COVID-19 vaccine clinical trials conducted by Pfizer/BioNTech.