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A Study to Evaluate the Safety, Tolerability, Pharmacokinetics (PK), and Immunogenicity of APG777 in Adults With Asthma
Sponsor: Apogee Therapeutics, Inc.
Summary
This is a multicenter, randomized, double-blind, placebo-controlled study to evaluate the safety, tolerability, PK, and immunogenicity of APG777 in adult participants with mild-to-moderate asthma. The duration of the study will be approximately 52 weeks (364 days) for each participant and will consist of a Screening Period, Treatment Period, and Follow-up Period.
Official title: A Phase 1b, Multicenter, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Immunogenicity of APG777 in Adults With Mild-to-Moderate Asthma
Key Details
Gender
All
Age Range
18 Years - 65 Years
Study Type
INTERVENTIONAL
Enrollment
31
Start Date
2025-03-27
Completion Date
2027-03
Last Updated
2026-02-17
Healthy Volunteers
No
Conditions
Interventions
APG777
APG777 subcutaneous injection
Placebo
Matching placebo subcutaneous injection
Locations (11)
Investigational Site
La Jolla, California, United States
Investigational Site
Long Beach, California, United States
Investigational Site
San Jose, California, United States
Investigational Site
Torrance, California, United States
Investigational Site
Normal, Illinois, United States
Investigational Site
Kansas City, Missouri, United States
Investigational Site
Edmond, Oklahoma, United States
Investigational Site
Philadelphia, Pennsylvania, United States
Investigational Site
Pittsburgh, Pennsylvania, United States
Investigational Site
Bradford, West Yorkshire, United Kingdom
Investigational Site
Manchester, United Kingdom