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Clinical trial

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

NCT01506375 is registered in ClinicalTrials.gov with BioTech Tools S.A. as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
Safety, Clinical Tolerability and Immunogenicity of gpASIT+TM Administered Subcutaneously to Hay Fever Patients Either Alone or in Presence of DnaK Immunoregulating Adjuvant
Lead sponsor
BioTech Tools S.A.
Phase
Phase 2
Overall status
Completed
Start date
November 30, 2011
Completion date
April 30, 2013
Enrollment
24 (actual)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

hay fever