Janssen Presented Results of RSV Vaccine in P-IIb CYPRESS Study for Lower Respiratory Tract Disease Due to Respiratory Syncytial Virus at IDWeek 2021

October 4, 2021 Auto Bot Clinical Trials, Janssen, P-IIb, respiratory syncytial virus 0

Shots:

  • The P-IIb CYPRESS study evaluates the efficacy & safety of RSV vaccine vs PBO in a ratio (1:1) in 5782 patients aged ≥65 with LRTD caused by RSV
  • The study met its 1EPs & 2EPs i.e., 80% efficacy against RSV-associated LRTD & 70% against any symptomatic RSV-associated ARI. The vaccine showed robust humoral & cellular immune responses & a substantial increase in RSV neutralizing Abs 14 days after vaccination & was generally well-tolerated
  • The company also initiates the P-III EVERGREEN study of RSV vaccine vs PBO in ~23000 adults aged ≥60yrs. for the same indication across North America, EU, Asia & Southern Hemisphere based on the results from the P-IIb CYPRESS study

Click here to­ read full press release/ article | Ref: J&J | Image: Clinical Trials Arena

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