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A Randomized, Double Blind, Comparative, Phase I Study To Evaluate The Safety, Tolerability And Immunogenicity Of Three Formulations (15µg Without Adjuvant, 7.5µg With Adjuvant And 3.75µg With Adjuvant) Of Monovalent H1N1 Influenza A (2009) Virus Vaccine In Healthy Adults. - H1N1Adults

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Trial Profile

A Randomized, Double Blind, Comparative, Phase I Study To Evaluate The Safety, Tolerability And Immunogenicity Of Three Formulations (15µg Without Adjuvant, 7.5µg With Adjuvant And 3.75µg With Adjuvant) Of Monovalent H1N1 Influenza A (2009) Virus Vaccine In Healthy Adults. - H1N1Adults

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 21 Jan 2019

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At a glance

  • Drugs Influenza A virus vaccine-H1N1 (Primary) ; Adjuvants
  • Indications Influenza A virus H1N1 subtype
  • Focus Adverse reactions; Pharmacodynamics
  • Sponsors Panacea Biotec

Most Recent Events

  • 13 Feb 2010 New trial record

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