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ACTIVE NOT RECRUITING
NCT06920901
PHASE1

A Study to Evaluate the Safety, Tolerability, Pharmacokinetics (PK), and Immunogenicity of APG777 in Adults With Asthma

Sponsor: Apogee Therapeutics, Inc.

View on ClinicalTrials.gov

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

DRUG

APG777

APG777 subcutaneous injection

DRUG

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