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Safety, Clinical Tolerability and Immunogenicity of gpASIT+TM Administered Subcutaneously to Hay Fever Patients Either Alone or in Presence of DnaK Immunoregulating Adjuvant.

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Trial Profile

Safety, Clinical Tolerability and Immunogenicity of gpASIT+TM Administered Subcutaneously to Hay Fever Patients Either Alone or in Presence of DnaK Immunoregulating Adjuvant.

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 07 Nov 2021

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At a glance

  • Drugs ABT 011 (Primary) ; DnaK
  • Indications Allergic rhinitis; Grass pollen hypersensitivity
  • Focus Adverse reactions
  • Sponsors BioTech Tools

    • Most Recent Events

    • 23 May 2014 According to ClinicalTrials.gov record, status changed from active, no longer recruiting to completed.
    • 01 Aug 2012 Planned End Date changed from 1 Jun 2012 to 1 Apr 2013 as reported by ClinicalTrials.gov.
    • 01 Aug 2012 Status changed from recruiting to active, no longer recruiting as reported by ClinicalTrials.gov.

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