Rotavirus, Live

drug
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Also known as RotateqRotaviruslive

Summary

Rotavirus, Live (CHEMBL6068358) is an approved vaccine component; indicated across 2 conditions including rotavirus infection.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Vaccine component
  • Indications: 2 conditions
  • Clinical trials: 11

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL6068358
NameRotavirus, Live
TypeVaccine component
Max phase4

Also known as: Rotateq, Rotavirus, live, ROTAVIRUS, LIVE

Targets

Targets

No target linkage available.

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

2 indications (2 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
Rotavirus infection4MONDO:0005194EFO:0002622

1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 11.

Phase distribution

PhaseTrials
PHASE37
PHASE42
PHASE21
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00740935PHASE4COMPLETEDImpact of Systematic Infants Vaccination Against Rotavirus on Gastroenteritis Hospitalization: a Prospective Study in Brest District, France.
NCT02847026PHASE4COMPLETEDFractional Inactivated Poliovirus Vaccine Booster and Rotavirus Study
NCT06736041PHASE3ACTIVE_NOT_RECRUITINGStudy of a 4-Dose Regimen of a 21-valent Pneumococcal Conjugate Vaccine in Healthy Infants From Approximately 2 Months of Age
NCT06824181PHASE3ACTIVE_NOT_RECRUITINGStudy of Mixed Vaccination Schedules With a 21-valent Pneumococcal Conjugate Vaccine and a 20-valent Pneumococcal Conjugate Vaccine in Healthy Infants From Approximately 2 Months of Age
NCT06824194PHASE3ACTIVE_NOT_RECRUITINGStudy of the Safety of a 21-valent Pneumococcal Conjugate Vaccine in Healthy Infants From Approximately 2 Months of Age
NCT01341639PHASE3COMPLETEDSafety, Tolerability, and Immunogenicity of V419 in Healthy Infants When Given at 2, 3, 4 and 12 Months (V419-007)
NCT01839175PHASE3COMPLETEDConcomitant Administration of a New Hexavalent Vaccine With a Meningococcal Serogroup C Conjugate Vaccine in Healthy Infants During Primary Series Immunisation Followed by Booster Vaccination
NCT02193061PHASE3COMPLETEDRandomized, Controlled Single-blind Clinical Study to Assess Vaccine Interchangeability Between RV5 and RV1 Using Seven Combined Anti-rotavirus Prevention Programs
NCT04481191PHASE3COMPLETEDImmunogenicity and Safety of Concomitant and Non-Concomitant Administration of RotaTeq® (V260) and Inactivated Poliomyelitis Vaccine in Healthy Chinese Infants (V260-074)
NCT00880698PHASE2COMPLETEDSafety and Immune Response of a Rotavirus Vaccine in HIV-infected and Uninfected Children Born to HIV-infected Mothers
NCT00836498PHASE1TERMINATEDA Study of the Safety and Immune Response to RotaTeq™ Vaccine in the Elderly (V260-027)

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).