Clinical Trials Logo

Ragweed Allergy clinical trials

View clinical trials related to Ragweed Allergy.

Filter by:
  • None
  • Page 1

NCT ID: NCT05346718 Recruiting - Allergic Rhinitis Clinical Trials

Threshold Concentrations for Ragweed and Birch Pollen in Seasonal Allergic Rhinitis

UBAMBI
Start date: September 1, 2022
Phase: N/A
Study type: Interventional

The ragweed Ambrosia artemisiifolia is spreading in northern Europe due to climate change. The pollen are considered highly allergenic and might trigger allergy symptoms at much lower concentrations than e.g. grass or birch pollen. This study aims to determine threshold concentrations for ragweed and birch pollen in patients with seasonal allergic rhinitis. Participants will be exposed in an allergen challenge chamber that was technically modified to maintain very low and stable pollen concentrations for several hours. The study design is adaptive, where the pollen concentrations are escalated or de-escalated based on interim analysis of resulting allergic symptoms.

NCT ID: NCT02396680 Completed - Rhinoconjunctivitis Clinical Trials

Ragweed-SPIRE Follow-On Study

Start date: April 2015
Phase: N/A
Study type: Observational

The purpose of this study is to determine the efficacy of Ragweed-SPIRE 12 months after the initial dose.

NCT ID: NCT01448603 Completed - Rhinoconjunctivitis Clinical Trials

ToleroMune Ragweed Follow up Study

Start date: October 2011
Phase: N/A
Study type: Observational

Ragweed is the primary cause of autumn allergies. The ragweed season begins in mid-August. In the third National Health and Nutrition Examination Surveys54.3% of the population had positive test responses to one or more allergens, with the prevalence for short ragweed being 26.2% The purpose of this observational follow-on study is to further evaluate rhinoconjunctivitis symptoms on exposure to ragweed allergen in the EEC among subjects who completed all dosing visits and the post treatment challenge (PTC) visit in study TR002 approximately one year after the start of treatment.

NCT ID: NCT01398137 Completed - Ragweed Allergy Clinical Trials

Ragweed Observational Study

Start date: July 2011
Phase: N/A
Study type: Observational

This is an observational to evaluate Total Rhinoconjunctivitis Symptom Score and rescue medication usage (as measured by Rescue Medication Score as a Combined Score to inform the design of a phase III field study with ToleroMune Ragweed.

NCT ID: NCT01361412 Completed - Ragweed Allergy Clinical Trials

Identification of Potential Biomarkers of Response to Peptide Immunotherapy for Ragweed Allergy

Start date: March 2011
Phase: Phase 2
Study type: Interventional

The aim of the study is to identify changes in potential biomarkers after peptide immunotherapy for that may subsequently be developed as biomarkers that correlate with clinical efficacy.

NCT ID: NCT01198613 Completed - Ragweed Allergy Clinical Trials

ToleroMune Ragweed Exposure Chamber Study

Start date: September 2010
Phase: Phase 2
Study type: Interventional

It is believe that ragweed is the primary cause of autumn allergies and 87% of patients with ragweed allergy suffer rhinoconjunctivitis. ToleroMune Ragweed is a novel, synthetic, allergen-derived peptide desensitising vaccine, currently being developed for the treatment of ragweed allergy. This study will look at the efficacy, safety and tolerability of two doses of ToleroMune Ragweed in ragweed allergic subjects following challenge with ragweed in an EEC.