Ozmosi | APG-808 Drug Profile
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APG-808

Alternative Names: APG-808, APG808, APG 808
Clinical Status: Active
Latest Update: 2025-12-06
Latest Update Note: Clinical Trial Update

Product Description

APG808, has been engineered to bind to and block IL-4Ra[EC1] to modulate dysregulated immune activity and to FcRn with high affinity to extend antibody half-life and potentially requiring less frequent dosing. IL-4Ra is a protein receptor that interacts with IL-13 and IL-4 as part of the body's natural inflammatory response. In COPD, this inflammatory signaling occurs more frequently and can trigger an exaggerated immune response. IL-4Ra is a well-established target for the treatment of COPD. (Sourced from: https://apogeetherapeutics.com/pipeline/)

Mechanisms of Action: IL4A Inhibitor

Novel Mechanism: Yes

Modality: Antibody

Route of Administration: N/A

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Company: Apogee Therapeutics
Company Location: Eastern America
Company Founding Year: 2022
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for APG-808

Countries in Clinic: Australia

Active Clinical Trial Count: 1

Recent & Upcoming Milestones

  • Clinical Outcomes Reported - Apogee Therapeutics presented P1 Asthma results on 2025-05-12 for APG-808
  • Clinical Outcomes Reported - Apogee Therapeutics announced they will present P1 Asthma results in 1H25 for APG-808
  • Clinical Outcomes Reported - Apogee Therapeutics presented P1 Healthy Volunteers results on 2024-12-02 for APG-808

Highest Development Phases

Phase 1: Asthma

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

ACTRN12624000238572

ACTRN12624000238572

P1

Completed

Asthma

2024-12-19

2026-02-15

Treatments