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项与 Parietaria pollen allergy immunotherapy(Laboratorios LETI SL) 相关的临床试验Prospective, Open Uncontrolled Study to Evaluate the Safety of Depigoid With Two Pollen Combinations (Grasses/Olea and Grasses/Parietaria)2000DPP/ml in Patients With Allergic Rhinitis or Rhinoconjunctivitis With or Without Seasonal Asthma.
The primary objective of this study is to evaluate the safety and tolerance of a rush build up administration of Depigoid forte pollen and the first maintenance dose administered 4 weeks later.
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
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.
100 项与 Parietaria pollen allergy immunotherapy(Laboratorios LETI SL) 相关的临床结果
100 项与 Parietaria pollen allergy immunotherapy(Laboratorios LETI SL) 相关的转化医学
100 项与 Parietaria pollen allergy immunotherapy(Laboratorios LETI SL) 相关的专利(医药)
100 项与 Parietaria pollen allergy immunotherapy(Laboratorios LETI SL) 相关的药物交易