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Johnson & Johnson Reports EUA Submission to the US FDA for Supporting the Booster of its Single Shot COVID-19 Vaccine Candidate

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Johnson & Johnson Reports EUA Submission to the US FDA for Supporting the Booster of its Single Shot COVID-19 Vaccine Candidate

Shots:

  • The submission is based on the P-III ENSEMBLE 2 study that evaluates the booster dose COVID-19 vaccine in adults aged ≥18yrs with COVID-19
  • The results demonstrated a 94% protection against symptomatic COVID-19 in the US for booster dose @56 days after primary dose & 100% protection against severe/critical COVID-19 @14 days post-booster vaccination
  • The company also submits the data from the P-I/IIa study which showed a substantial increase in Ab levels 9-fold at 1wks. when a booster of COVID-19 vaccine was given 6mos. after the single shot & continues to increase to a 12-fold at 4wks. The single-shot vaccine showed durable immune responses & was well-tolerated

Ref: J&J | Image: Nguoi Lad Dong

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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