This study will assess the efficacy and safety of ACT-129968 in adolescent, adult and elderly patients with seasonal allergic rhinitis, due to mountain cedar pollen.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
630
daily tablets
matching placebo tablets and capsules
daily capsules
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
The mean change in Daytime Nasal Symptom Score
Time frame: baseline to end of treatment period (2 weeks)
The mean change in other daytime/nighttime symptom scores of allergic rhinitis
Time frame: baseline to end of treatment period (2 weeks)
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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