The European Medicines Agency has begun evaluating an application for the use of a booster dose of Moderna’s (Nasdaq: MRNA) coronavirus vaccine, Spikevax.
The USA-based firm wants to offer the booster for administration at least six months after a second dose, in people aged 12 years and older.
The regulator’s human medicines committee (CHMP) is expected to carry out an accelerated assessment of data submitted by Moderna, including results from an ongoing clinical trial.
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