Phase 1 Study Evaluating Safety and Pharmacokinetics of ASY202 in Adults With Asthma
Start Date
5/26/2026
Completion Date
12/1/2026
Summary
This is a phase 1 study, randomized, double-blind, placebo-controlled, 2 treatment, 2 period crossover study to evaluate the pharmacokinetics, safety, and tolerability of a single inhaled dose of ASY202 in adults with stable asthma. Following screening, eligible participants will be enrolled and randomized to one of two treatment sequences. Participants will receive a single inhaled dose of ASY202 and a single inhaled dose of placebo, each administered once during separate study periods. During each treatment period, subjects will stay in the clinical research unit for safety monitoring and PK assessments, including serial blood sampling, spirometry, vital signs, clinical laboratory tests, and ECGs. Each period will include post dose assessments for up to 24 hours. Participants will return for their next treatment period after a washout interval to ensure complete clearance of study medication. All subjects will receive both treatments over the course of the study. A follow-up visit will occur after the last dose to assess ongoing safety and tolerability.
Eligibility Criteria
Age Range: 18 years to 55 years
Interventions
ASY202
Placebo
Conditions
Locations
Sun City Clinical Research
Glendale, Arizona 85304
United States
CenExel- Anaheim Clinical trials LLC
Anaheim, California 92801
United States
Worldwide Clinical Trials- Early Phase Research Unit
San Antonio, Texas 78217
United States