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Terminated Phase 3 Interventional

A 52-week, Placebo-controlled Study to Evaluate the Efficacy and Safety of 2 Doses of CHF6001 DPI (Tanimilast), as add-on to Maintenance Triple Therapy in Subjects With COPD and Chronic Bronchitis (PILASTER)

ClinicalTrials.gov ID: NCT04636801

Public ClinicalTrials.gov record NCT04636801. 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 Oct 20, 2026, 11:43 PM EDT

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

Official title

A 52-week, Randomized, Double-blind, Placebo-controlled, Parallel-group, Study to Evaluate the Efficacy and Safety of Two Doses of CHF6001 DPI add-on to Maintenance Triple Therapy in Subjects With Chronic Obstructive Pulmonary Disease (COPD) and Chronic Bronchitis

Brief summary

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

The purpose of the study is to evaluate the efficacy and safety of two doses of CHF6001 (Tanimilast), as add-on to maintenance triple therapy in the target patient population.

Study identification

NCT ID
NCT04636801
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Chiesi Farmaceutici S.p.A.
Industry
Enrollment
4,710 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 Years and older
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 14, 2021 (Actual)
Primary completion
Oct 31, 2025 (Actual)
Completion
Oct 31, 2025 (Actual)
Last update posted
Dec 17, 2025

2021 – 2025

United States locations

U.S. sites
15
U.S. states
7
U.S. cities
12
Facility City State ZIP Site status
Chiesi Clinical Trial - Site 840402 Sheffield Alabama 35660-4020 —
Chiesi Clinical Trial - Site 840480 Northridge California 91324-6200 —
Chiesi Clinical Trial - Site 840487 Cutler Bay Florida 33189-1230 —
Chiesi Clinical Trial - Site 840404 Hollywood Florida 33021 —
Chiesi Clinical Trial - Site 840407 Miami Florida 33144-2100 —
Chiesi Clinical Trial - Site 840444 Miami Florida 33144 —
Chiesi Clinical Trial - Site 840437 Miami Florida 33165-2075 —
Chiesi Clinical Trial - Site 840403 Miami Florida 33175-3598 —
Chiesi Clinical Trial - Site 840463 Orlando Florida 32822-5806 —
Chiesi Clinical Trial - Site 840401 Peachtree Corners Georgia 30071-2656 —
Chiesi Clinical Trial - Site 840478 New Windsor New York 12553-7754 —
Chiesi Clinical Trial - Site 840483 Philadelphia Pennsylvania 19140 —
Chiesi Clinical Trial - Site 840474 Kerrville Texas 78028-9640 —
Chiesi Clinical Trial - Site 840409 Plano Texas 75025 —
Chiesi Clinical Trial - Site 840481 San Antonio Texas 78229 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 432 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04636801, 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 Dec 17, 2025 · Synced Oct 20, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04636801 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →