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NCT05161845

Clinical Trial of Measles, Mumps and Rubella Combined Vaccine, Live

Completed Phase 4 Last updated 14 August 2023
What this trial tests

Phase 4 trial testing Measles, Mumps and Rubella Combined Vaccine, Live in Immunotoxicity in 1,068 participants. Completed in 1 October 2022.

Timeline
23 December 2021
Primary endpoint
4 April 2022
1 October 2022

Quick facts

Lead sponsorShanghai Institute Of Biological Products
PhasePhase 4
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeprevention
Enrollment1,068
Start date23 December 2021
Primary completion4 April 2022
Estimated completion1 October 2022
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Shanghai Institute Of Biological Products

Who can join

Adults 8 Months to 12 Months, any sex, with Immunotoxicity or Vaccine. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To evaluate the immunogenicity, lot-to-lot consistency and safety of three consecutive batches of Measles, Mumps and Rubella Combined Vaccine, Live.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Immunotoxicity

Currently open trials in the same condition.

Other Shanghai Institute Of Biological Products trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05161845.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing