Stopped: The reason is: emerging pre-clinical toxicology findings.
This is a Phase IIa, double blind, randomized, parallel group, placebo controlled multi centre study to evaluate the effect of AZD8154 (administered via nebulizer daily \[QD\]) on allergen-induced inflammation in subjects with mild allergic asthma challenged with an inhaled allergen. Approximately 36 subjects who meet all eligibility criteria will be randomized (1:1) to receive either AZD8154 or placebo.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Maximal percentage decrease in forced expiratory volume in 1 second (FEV1) 3-7 hours post-allergen challenge
Timeframe: At day 9
Area under the curve (AUC) of time adjusted percent decrease in FEV1 in late asthmatic response (LAR) 3-7hr
Timeframe: At day 9