Clinical Trial Search

Primary: Number of Participants With the Composite Primary Outcome — 46; 37 Participants — p=0.42

Primary: Number of CMV Seropositive Subjects With Appearance or Increase of Anti-CMV Tegument Protein IgG Antibodies in Serum. — 5; 2 Participants

Primary: Number of Subjects With Any Cytomegalovirus (CMV) Congenital Infection — 24; 20; 4; 58 Participants

Primary: Number of Participants From Each Arm Who Received Influenza Vaccine — 33; 37; 8 Participants

Primary: Number of Patients With Late CMV Disease — 0; 0 Participants

Primary: Number of Participants With Clinically Significant CMV Reactivation or CMV Disease — 62; 89; 78; 32 Participants

Primary: Time to Engraftment (Days) Stratified by CMV DNaemia Occurring Before or After Neutrophil's Engraftment — 17; 19 days

Primary: Number of Participants With a Complete Response — 8; 50 Participants

Primary: Number of Participants With Clinically Significant CMV Infection Through Week 24 Post-Transplant — 155; 78 Participants

Primary: Change in Best Ear Hearing Assessments at 6 Months. — 3; 5; 37; 36 participants

Primary: Complete Response — 20; 57 Participants

Primary: Number of Participants With Non-Relapse Mortality — 0 Participants

Primary: Clinically Significant CMV Viremia for Hematopoietic Cell Transplantation/HCT Participants in the Interventional Cohort Only — 5; 0; 31; 0 Participants

Primary: Number of Ears That Had (1) Improved Hearing or no Change in Hearing (2) Worsened Hearing. — 27; 20; 1; 6 Ears — p=0.0859

Primary: Virological Response on Treatment Week 6 — 5 Participants

Primary: Number of Participants With Clinically Significant CMV Infection — 13; 4; 6; 4 Participants

Primary: Percentage of Patients Who Developed Cytomegalovirus (CMV) Disease up to Month 12 Post-transplant — 43.6; 23.9 Percentage of patients — p=<=0.0002

Primary: Proportion of Patients Developing Cytomegalovirus (CMV) Disease Within 6 Months of Liver Transplantation Under Valcyte Prophylaxis — 3 participants

Primary: Number of Participants With Adverse Events — 1; 31; 1; 22 Participants

Primary: Serum IL-6 Level — -0.79; -0.79 pg/mL

Primary: Number of Participants With Local and Systemic Adverse Events During Seven-Day Follow-Up Period — 11; 14; 13; 5 Participants

Primary: The Prevalence of CMV Shedding in Saliva, Urine and Vaginal Secretions of CMV Seropositive Women in Pregnancy — 27; 4; 16; 20 Participants

Primary: a) CMV Viral Load — 100; 97.6; 86.36; NA percentage of agreement

Primary: Cellular Immune Response in Vaccine Recipients — 14 participants

Primary: Concentrations of Antibodies Against Anti-Glycoprotein B (gB) Immunoglobulin G (IgG) — 5091.4; 5495.1; 2587.2 EL.U/mL

Primary: Change in %CD38+ Human Leukocyte Antigen-D-related (HLA-DR)+ CD8+ T Cells From Baseline to Week 8. — 1.3; -4.0 percentage of activated T cells

Primary: Number of Participants With Solicited Local and Systemic Adverse Reactions (ARs) — 33; 59; 40; 12 Participants

Primary: Percentage of Participants With Active Cytomegalovirus (CMV) Infection Within 12 Months — 14.1; 42.6 percentage of participants

Primary: Percentage of Participants Who Achieved Confirmed Clearance of Plasma CMV Deoxyribose Nucleic Acid (DNA) at Week 8 — 68.3 percentage of participants

Primary: The Number of Participants Who Have Completed >90% of Their Recommended Cytomegalovirus (CMV) Monitoring Tests in the DBS and Control Arms in the ITT Population — 27; 15…