This Phase II, double-blind, placebo-controlled, randomized, parallel-group study is designed to evaluate the efficacy, safety and tolerability of MEMP1972A when administered to patients by intravenous (IV) infusion for the treatment of allergen-induced asthma.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
29
Unnamed facility
Calgary, Alberta, Canada
Unnamed facility
Edmonton, Alberta, Canada
Unnamed facility
Vancouver, British Columbia, Canada
Unnamed facility
Hamilton, Ontario, Canada
Late airway response (LAR) area under the concentration-time curve (AUC) (percent decline in forced expiratory volume in 1 second [FEV1] over time)
Time frame: Between 3 and 7 hours after allergen challenge at Day 86 after the first dose
Maximum percent decline in FEV1
Time frame: Immediately prior to the allergen challenge to between 3 and 7 hours after allergen challenge on Day 86 after the first dose
Change in methacholine challenge PC20 relative to the pre-allergen challenge PC20
Time frame: Day 87
Maximum percent decline in FEV1 and early airway response (EAR) AUC (percent decline in FEV1 over time)
Time frame: Between 0 and 3 hours after post-treatment allergen challenge
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Unnamed facility
Ste. Foy, Quebec, Canada
Unnamed facility
Saskatoon, Saskatchewan, Canada
Unnamed facility
Stockholm, Sweden