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NCT03572491

Preventive Effectiveness, Safety and Immunogenicity of a Allantoic Split Inactivated Seasonal Influenza Vaccine

Completed Phase 3 Last updated 28 June 2018
What this trial tests

Phase 3 trial testing influenza vaccine in Human Influenza in 2,000 participants. Completed in 21 May 2018.

Timeline
18 September 2017
Primary endpoint
21 May 2018
21 May 2018

Quick facts

Lead sponsorResearch Institute for Biological Safety Problems
PhasePhase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeprevention
Enrollment2,000
Start date18 September 2017
Primary completion21 May 2018
Estimated completion21 May 2018
Sites1 location across Kazakhstan

Drugs / interventions tested

Conditions studied

Sponsor

Research Institute for Biological Safety Problems

Who can join

18 and older, any sex, with Human Influenza. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The study is Multicenter, phase 3, Open-Label trial that explored the preventive effectiveness, safety and immunogenicity of single dose a allantoic split inactivated seasonal influenza vaccine in healthy adults.

Publications & conference data

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

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Other trials of influenza vaccine

Trials testing the same drug.

Other recruiting trials for Human Influenza

Currently open trials in the same condition.

Other Research Institute for Biological Safety Problems 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/NCT03572491.

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