This is a multicenter, randomized, double-blind, placebo-controlled study designed to demonstrate the safety and efficacy of MILR1444A compared with placebo in reducing the airway reaction to an inhaled aeroallergen solution in adult patients with mild allergic asthma. The study will randomize approximately 24 patients at five study centers. In the event of patient discontinuation from the study, additional patients may be enrolled at the discretion of the Sponsor.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
29
Repeating subcutaneous injection
Repeating subcutaneous injection
Late asthmatic response (LAR)
Time frame: Day 92
Early asthmatic response (EAR)
Time frame: Day 92
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.