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