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Safety, clinical tolerability and immunogenicity of increasing doses of gpASIT+TM administered subcutaneously to hay fever patients. A Phase IIa dose-escalation study.

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Safety, clinical tolerability and immunogenicity of increasing doses of gpASIT+TM administered subcutaneously to hay fever patients. A Phase IIa dose-escalation study.

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 07 Nov 2021

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At a glance

  • Drugs ABT 011 (Primary)
  • Indications Seasonal allergic rhinitis
  • Focus Adverse reactions
  • Sponsors BioTech Tools

    • Most Recent Events

    • 10 Jan 2018 Results assessing the tolerability of grass pollen allergy immunotherapy in patients with seasonal allergic rhinitis, were published in the Allergy.
    • 05 Jun 2014 New source identified and integrated (ClinicalTrials.gov: NCT02156791)
    • 05 Jun 2014 According to the ClinicalTrials.gov record, status changed from recruiting to completed.

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