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Rotavirus infection

1 published article · Updated continuously

Clinical Trial Landscape

Clinical Trials for Rotavirus infection

5 trials tracked for Rotavirus infection: 3 in phase 3 or 4 and 1 with published results. The most-cited published study has 14 citations.

5Trials tracked
3Phase 3 & 4
0Recruiting
1With published results
Phase distribution
Phase 4 2 Phase 3 1 Phase 2 1 Phase 1 1
  1. Phase 4 The Effects of Increased Inoculum on Oral Rotavirus Vaccine Take and Immunogenicity Completed · 14 cited
  2. Phase 4 Safety and Immunogenicity of Sequential Rotavirus Vaccine Schedules Completed
  3. Phase 3 This Study Will Evaluate the Immunogenicity, Reactogenicity and Safety of the Routine Infant Vaccines Pediarix®, Hiberix® and Prevenar 13® When Co-administered With GlaxoSmithKline (GSK) Biologicals' Liquid Human Rotavirus Vaccine (HRV) as Compared to GSK's Licensed Lyophilized Vaccine Completed
  4. Phase 2 Safety and Immune Response of a Rotavirus Vaccine in HIV-infected and Uninfected Children Born to HIV-infected Mothers Completed
  5. Phase 1 A Phase 1 Dose Escalation Study to Examine the Safety of the P2-VP8 Rotavirus Vaccine Completed

Showing the 5 most-cited and recently-updated of 5 trials. Browse the full registry →

Trial data sourced from ClinicalTrials.gov. Counts describe the research landscape and are not a treatment recommendation. Informational only — not medical advice.

What the trials found For clinicians

Rotavirus infection: what the trials found

Rotarix administration demonstrates significant immunogenicity in infants. Evidence shows high rates of successful vaccine take, defined as either positive fecal vaccine-strain virus shedding or rotavirus-specific plasma IgA seroconversion 1.

The Rotarix vaccine is associated with robust seroprotection and antibody responses. Specifically, subjects demonstrated anti-polyribosyl ribitol phosphate (Anti-PRP) antibody concentrations above the 0.15 µg/mL cut-off, as well as significant seroprotection at the 1.0 µg/mL threshold 3. Furthermore, Rotarix elicited statistically significant seroprotective responses to Anti-PT, Anti-FHA, and Anti-PRN antibodies (p=<.0001) 3.

Safety profiles for Rotarix have been established in large cohorts; studies observed a range of solicited systemic reactions within 8 days post-vaccination across various study arms 2.

Recent results — preliminary, needs further review

  • RotaTeq showed varying responder rates as measured by serum Anti-rotavirus IgA ELISA and Serum Neutralizing Antibodies (SNA) G1, G2, G3, G4 and P1 (p=<0.001) 4.
  • The P2-VP8 subunit rotavirus vaccine showed no statistically significant difference in maximum severity of adverse events or local/systemic reactogenicity across study arms 5.

For the clinician treating this condition

  • Rotarix provides consistent seroprotection and high rates of successful vaccine take via IgA seroconversion or fecal shedding [1, 3].
  • Rotarix is associated with a documented profile of solicited systemic reactions within the first week of administration 2.

AI synthesis of 5 cited trials, updated Jul 5, 2026. Informational only — not medical advice; trial data sourced from ClinicalTrials.gov. How we use AI.

HCP Mode — summaries include clinical detail, trial data, and statistical outcomes.
Patient Mode — summaries use plain language, avoiding clinical jargon.