GMCs of Anti-Pneumococcal PS Antibodies Reported in This Study, Compared With Those Published for 4-Dose Schedules of PCV Used in Efficacy Trials in Finland (FinOM Trial) and the United States ...
Advancement to Stage 2 of Infant Study Supported by Review of Stage 1 Safety and Tolerability Data -- -- Company Expects to ...
Vaxcyte has advanced to the Phase II trial’s second and final stage (Stage 2) assessing its 31-valent pneumococcal conjugate ...
The Committee for Medicinal Products for Human Use (CHMP) has recommended that Capvaxive be used to prevent invasive disease ...
Vaxcyte's new pneumococcal vaccine may only have phase ... which targets 20 common serotypes, but at the highest dose tested generated stronger protection on 18 out of 20 of them – and for ...
The dosage of tetracycline was 1 gm ... Those in whom the diagnosis of pneumococcal pneumonia could not be substantiated were subsequently excluded. The criteria for the diagnosis of pneumococcal ...
“Invasive pneumococcal disease and pneumococcal pneumonia remain critical public health challenges worldwide,” said Dr. Paula Annunziato, senior vice president, infectious diseases and ...
The PCV was well tolerated. Conclusion: The pneumococcal antibody concentrations at 13 months were comparable with those noted previously with the 4-dose schedule. The results suggest that the ...
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