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Hypersensitivity, Immediate clinical trials

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NCT ID: NCT00580606 Completed - Hypersensitivity Clinical Trials

A Randomized, Double-Blind Placebo-Controlled Peanut Sublingual Immunotherapy Trial

Start date: December 2007
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and immune response to daily sublingual (under the tongue) immunotherapy (SLIT) with peanut extract in adults and children with peanut allergies.

NCT ID: NCT00461097 Completed - Hypersensitivity Clinical Trials

Oral Immunotherapy for Childhood Egg Allergy

Start date: May 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if oral immunotherapy (OIT) will desensitize a child with an allergy to egg and eventually lead to the development of tolerance to egg.

NCT ID: NCT00423787 Completed - Clinical trials for Type I Hypersensitivity

Efficacy and Safety/Tolerability of Ragweed MATA MPL

Start date: March 2007
Phase: Phase 3
Study type: Interventional

Ragweed MATAMPL has been developed by Allergy Therapeutics to provide pre-seasonal specific immunotherapy for patients with proven type I hypersensitivity to cross reacting ragweed pollens causing rhinitis and/or conjunctivitis with or without mild to moderate asthma bronchiale. The purpose of this study is to compare the efficacy of Ragweed MATAMPL versus placebo in ragweed-allergic subjects following 4 subcutaneous injections of study medication administered before the start of the 2007 ragweed pollen season

NCT ID: NCT00414141 Completed - Clinical trials for Type I Hypersensitivity

Efficacy and Safety/Tolerability of Grass MATA MPL

Start date: November 2006
Phase: Phase 3
Study type: Interventional

Grass MATA MPL has been developed by Allergy Therapeutics (UK) Ltd. to provide pre-seasonal specific immunotherapy for patients with proven type I hypersensitivity to cross reacting grass pollens causing rhinitis and/or conjunctivitis with or without mild to moderate asthma bronchiale. The purpose of this study is to compare the efficacy of Grass MATA MPL versus placebo in grass-allergic subjects following 4 subcutaneous injections of study medication administered before the start of the 2007 grass pollen season.

NCT ID: NCT00387478 Terminated - Clinical trials for Type I Hypersensitivity

Investigation of Efficacy and Safety of Tree MATAMPL,Tree MATA, and Placebo in Patients With Birch-Induced Seasonal Allergic Rhinitis

Start date: October 2006
Phase: Phase 2
Study type: Interventional

Tree MATAMPL has been developed to provide pre-seasonal specific immunotherapy for patients with hypersensitivity to Tree (birch, alder, hazel) pollen (hay fever). This novel formulation is designed to provide a vaccine that will be efficacious with only four escalating dose injections administered before the start of the pollen season. In this Study the Efficacy will be assessed by exposing allergic subjects to birch pollen in an environmental exposure chamber EEC. Patient symptomatic response to birch pollen and patient quality of life in the EEC will be determined.

NCT ID: NCT00325338 Completed - Clinical trials for Type I Hypersensitivity

Follow-up Investigation of Efficacy of Ragweed MATAMPL,and Placebo in Patients With Ragweed-induced Seasonal Allergic Rhinitis

Start date: May 2006
Phase: Phase 2
Study type: Interventional

Ragweed MATAMPL has been developed to provide pre-seasonal specific immunotherapy for patients with hypersensitivity to ragweed pollen (hay fever). This novel formulation is designed to provide a vaccine that will be efficacious with only four escalating dose injections administered before the start of the pollen season. In this Follow-up Study the Efficacy will be assessed by exposing allergic subjects to Ragweed pollen in an environmental exposure chamber EEC. Patient symptomatic response to pollen and patient quality of life in the EEC will be determined. Patients who previously completed two EEC portions of study Ragweed MATAMPL 204 and who had been treated with either Ragweed MATA MPL or Placebo before the 2005 ragweed season will be enrolled.

NCT ID: NCT00312312 Recruiting - Allergic Rhinitis Clinical Trials

Allergy Towards Grass and Bronchial Inflammation - Related to Immunotherapy and Exhaled Nitrogen Oxide

Start date: March 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the immunomodulatory effect of treatment of allergic rhinitis symptoms with specific immunotherapy by measurement of pulmonary inflammatory markers, and among others, exhaled nitric oxide.

NCT ID: NCT00258635 Completed - Clinical trials for Type I Hypersensitivity

Investigation of Safety+Efficacy of Different Doses of RagweedMATAMPL;Assessment of Residual Allergenicity Using Skin Prick Test

Start date: November 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the immunological differences between three RagweedMATAMPL treatment arms compared to placebo with respect to immunoglobulin levels. In addition, the study will assess the reduced allergenicity of modified Ragweed Pollen contained in RagweedMATAMPL compared to unmodified native allergen using skin prick testing.

NCT ID: NCT00241410 Completed - Clinical trials for Type I Hypersensitivity

Safety, Immunological Effect and Efficacy of the Combined Application of MPL and Grass Pollen Allergen

Start date: December 2005
Phase: Phase 1
Study type: Interventional

Safety and tolerability of different dose combinations of MPL and grass pollen allergen and to identify the highest combinations of MPL and grass pollen allergen which is safe. Pharmacodynamics and efficacy of MPL and grass pollen allergen.

NCT ID: NCT00133159 Completed - Clinical trials for Type I Hypersensitivity

Different Doses of Tyrosine Adsorbed Grass Pollen Allergoid With Monophosphoryl Lipid A (MPL) in Patients Sensitized to Grass Pollen

Start date: September 12, 2005
Phase: Phase 2
Study type: Interventional

Allergen-specific immunotherapy (SIT), the administration of gradually increasing quantities of an allergen extract to an allergic patient, is a curative approach which directly treats the underlying allergic disease. GrassMATAMPL has been developed to provide pre-seasonal specific immunotherapy for patients with an allergy to grass pollen (hay fever). The purpose of this double-blind Phase IIb study is to assess the tolerability and immunogenicity of different doses of GrassMATAMPL in volunteers allergic to grasses and rye pollen.