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Moderna's Spikevax Receives TGA's Provisional Approval to Treat COVID-19 in Patients Aged 12-17 Years

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Moderna's Spikevax Receives TGA's Provisional Approval to Treat COVID-19 in Patients Aged 12-17 Years

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  • TGA has provisionally approved the use of Moderna’s Spikevax (elasomeran) in individuals aged ≥12yrs. The decision follows the provisional approval granted by the TGA to Spikevax on Aug 09- 2021 for use in individuals aged ≥18yrs.
  • Provisional approval for this group follows the data supporting the efficacy & safety of the vaccine. The recommended dose and dose interval is like that of the adult population – 2 full doses given 28 days apart
  • The vaccine has received regulatory approval in this age group in several jurisdictions- including the UK- Canada- the EU- and Switzerland. TGA has secured 25M doses of Spikevax to diversify Australia's vaccine portfolio as well as provide access to a booster or variant vaccine

  | Ref: TGA | Image: Moderna

Click here to­ read the full press release 

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This content piece was prepared by our former Senior Editor. She had expertise in life science research and was an avid reader. For any query reach out to us at connect@pharmashots.com

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