Stopped: Sponsor Decision - terminated due to changes in company priorities and not related to safety concerns.
Study JSP-CP-012 is designed as a proof of concept, parallel-group, single dose, double blind, placebo-controlled study using an allergen challenge model. A single dose proof of concept approach at a dose level shown to be biologically active should inform the impact of briquilimab on allergic asthma as compared to placebo while minimizing exposure to participants, in a new indication.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
To evaluate the safety and tolerability of briquilimab in mild-to-moderate asthmatic participants
Timeframe: From signing the informed consent form (ICF) through end of trial (EOT) visit (up to 4.5 months)
To compare the effect of treatment with briquilimab vs placebo on the allergen-induced LAR
Timeframe: 3-7 hours after allergen challenge between Briquilimab and Placebo at week 6
To compare the effect of treatment with briquilimab vs placebo on the allergen-induced LAR
Timeframe: 3-7 hours after allergen challenge between Briquilimab and Placebo at week 6