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Clinical, Multi-centre, Randomised, Double-blind Placebo-controlled Subcutaneous Immunotherapy Trial With Depigmented, Polymerized Extract of Parietaria Judaica Pollen on Patients With Hypersensitivity to This Pollen

NCT00916760 Phase 3 COMPLETED

The objective of this trial is to assess the clinical efficacy of the modified extract (depigmented and polymerized with glutaraldehyde) of the subcutaneous injection of Parietaria Judaica pollen in the treatment of patients affected by allergic rhinitis/rhinoconjunctivitis ( with or without episodic asthma) induced by hypersensitivity to grass pollen, evaluating the score regarding symptoms and consumption of the medication.

Details

Lead sponsorLaboratorios Leti, S.L.
PhasePhase 3
StatusCOMPLETED
Enrolment153
Start date2008-02
Completion2013-02

Conditions

Interventions

Primary outcomes

Countries

Spain