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Active, not recruiting Phase 2 Interventional

A Study to Assess the Effects of Dexpramipexole in Participants With Eosinophilic COPD

ClinicalTrials.gov ID: NCT06533553

Public ClinicalTrials.gov record NCT06533553. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 7:56 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-label Phase II Study to Assess the Pharmacodynamic (PD) Effects of Dexpramipexole in Participants With Eosinophilic Chronic Obstructive Pulmonary Disease (COPD)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is an open-label Phase II study assessing the PD of dexpramipexole 150 mg twice daily (BID) in participants with eosinophilic COPD. This study will help characterize the profile and duration of reductions of blood absolute eosinophil counts (AEC).

Study identification

NCT ID
NCT06533553
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Areteia Therapeutics
Industry
Enrollment
30 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 Years to 80 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 8, 2024
Primary completion
Sep 30, 2025
Completion
Nov 30, 2025
Last update posted
May 13, 2025

2024 – 2025

United States locations

U.S. sites
23
U.S. states
15
U.S. cities
22
Facility City State ZIP Site status
Research Site US-10001-017 Conway Arkansas 72032
Research Site US-10001-008 Newport Beach California 92663
Research Site US-10001-022 Northridge California 91324
Research Site US-10001-016 Westminster California 92683
Research Site US-10001-030 Orlando Florida 32803
Research Site 10001-032 Champaign Illinois 61820
Research Site US-10001-021 Hammond Indiana 46324
Research Site US-10001-033 Des Moines Iowa 50266
Research Site US-10001-020 Baltimore Maryland 21224
Research Site US-10001-024 Farmington Hills Michigan 48336
Research Site US-10001-005 Saint Charles Missouri 63301
Research Site US-10001-001 St Louis Missouri 63110
Research US-10001-010 Charlotte North Carolina 28277
Research Site US-10001-025 Charlotte North Carolina 28293
Research Site US-10001-007 Gastonia North Carolina 28054
Research Site US-10001-004 Columbus Ohio 43215
Research Site US-10001-002 DuBois Pennsylvania 15801
Research Site US-10001-013 Philadelphia Pennsylvania 19140
Research Site US-10001-023 East Providence Rhode Island 02914
Research Site US-10001-012 Rock Hill South Carolina 29732
Research Site US-10001-009 Corsicana Texas 75110
Research Site US-10001-038 Houston Texas 77030
Research Site 10001-026 McKinney Texas 75069

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06533553, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 13, 2025 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06533553 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →