Study of ACT-129968 in Adult Patients With Seasonal Allergic Rhinitis
Completed · Phase 2 · Has a placebo group
Conditions studied: Seasonal Allergic Rhinitis
In brief
This study will assess the efficacy and safety of different doses of ACT-129968 in adult patients with seasonal allergic rhinitis, due to mountain cedar pollen.
Key facts
- Study ID
- NCT01241214
- Run by
- Idorsia Pharmaceuticals Ltd.
- People needed
- 579
- Starts
- 2010-11-01
- Expected to finish
- 2011-02-01
- Last updated by the study team
- 2019-05-15
Who can join
Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Males and females aged 18 to 70 years.
- Clinical history of symptomatic seasonal allergic rhinitis associated with mountain cedar pollen for the last two years.
- Adequate exposure to mountain cedar pollen.
- Positive skin prick test to mountain cedar allergen within 12 months of screening.
- Sufficient nasal symptom score during a run-in period.
You may not qualify if…
- Non-allergic rhinitis.
- Bacterial or viral respiratory tract infection.
- Chronic respiratory disorders.
- Asthma requiring treatment other than inhaled short-acting Beta2-agonists.
- Ocular infections or surgery, nasal obstruction, nasal biopsy or surgery, sinus surgery or perforation.
- Smoking within the last year.
- Ongoing or recent treatment for seasonal allergic rhinitis.
- Initiation of allergen immunotherapy within 6 months of screening.
Where it is running
- Clinical Investigative Site 7905 — Austin, Texas, United States
- Clinical Investigative Site 7907 — Kerrville, Texas, United States
- Clinical Investigative Site 7903 — New Braunfels, Texas, United States
- Clinical Investigative Site 7901 — San Antonio, Texas, United States
- Clinical Investigative Site 7902 — San Antonio, Texas, United States
- Clinical Investigative Site 7904 — San Antonio, Texas, United States
- Clinical Investigative Site 7906 — San Antonio, Texas, United States
Full record on ClinicalTrials.gov
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