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Clinical trialNCT04636814TerminatedPhase 3Interventional

A 52-week, Placebo- and Active- Controlled (Roflumilast, Daliresp® 500µg) Study to Evaluate the Efficacy and Safety of Two Doses of CHF6001 DPI (Tanimilast) as add-on to Maintenance Triple Therapy in Subjects With COPD and Chronic Bronchitis. (PILLAR)

SponsorChiesi Farmaceutici S.p.A.Enrollment3,973Chronic Obstructive Pulmonary Disease
View the registry record on ClinicalTrials.gov

Summary

The registered summary isn't in our current data snapshot. Read it on the ClinicalTrials.gov record ↗. Why? →

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

460 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Argentina
  • Chiesi Clinical Trial - Site 32502

    Buenos Aires, Argentina

  • Chiesi Clinical Trial - Site 32510

    Buenos Aires, Argentina

  • Chiesi Clinical Trial - Site 32515

    Buenos Aires, Argentina

  • Chiesi Clinical Trial - Site 32565

    Buenos Aires, Argentina

  • Chiesi Clinical Trial - Site 32514

    Ciudad Autonoma Buenos Aires, Argentina

  • Chiesi Clinical Trial - Site 32567

    Ciudad Autonoma Buenos Aires, Argentina

  • Chiesi Clinical Trial - Site 32507

    Ciudad Autónoma de Buenos Aire, Argentina

  • Chiesi Clinical Trial - Site 32563

    Concepción del Uruguay, Argentina

  • Chiesi Clinical Trial - Site 32503

    Córdoba, Argentina

  • Chiesi Clinical Trial - Site 32509

    Córdoba, Argentina

  • Chiesi Clinical Trial - Site 32501

    Florida, Argentina

  • Chiesi Clinical Trial - Site 32562

    Mar del Plata, Argentina

  • Chiesi Clinical Trial - Site 32505

    Mendoza, Argentina

  • Chiesi Clinical Trial - Site 32511

    Mendoza, Argentina

  • Chiesi Clinical Trial - Site 32513

    Mendoza, Argentina

  • Chiesi Clinical Trial - Site 32506

    Quilmes, Argentina

  • Chiesi Clinical Trial - Site 32553

    Rosario, Argentina

  • Chiesi Clinical Trial - Site 32508

    San Juan Bautista, Argentina

  • Chiesi Clinical Trial - Site 32512

    San Miguel de Tucumán, Argentina

  • Chiesi Clinical Trial - Site 32551

    San Miguel de Tucumán, Argentina

  • Chiesi Clinical Trial - Site 32561

    San Miguel de Tucumán, Argentina

  • Chiesi Clinical Trial - Site 32564

    San Miguel de Tucumán, Argentina

  • Chiesi Clinical Trial - Site 32566

    San Rafael, Argentina

  • Chiesi Clinical Trial - Site 32556

    Santa Fe, Argentina

Austria
  • Chiesi Clinical Trial - Site 40502

    Feldbach, Austria

  • Chiesi Clinical Trial - Site 40504

    Grieskirchen, Austria

  • Chiesi Clinical Trial - Site 40501

    Linz, Austria

  • Chiesi Clinical Trial - Site 40503

    Linz, Austria

  • Chiesi Clinical Trial - Site 40505

    Wels, Austria

Bosnia and Herzegovina
  • Chiesi Clinical Trial - Site 70553

    Banja Luka, Bosnia and Herzegovina

  • Chiesi Clinical Trial - Site 70555

    Bihać, Bosnia and Herzegovina

  • Chiesi Clinical Trial - Site 70554

    Bijeljina, Bosnia and Herzegovina

  • Chiesi Clinical Trial - Site 70557

    Foca, Bosnia and Herzegovina

  • Chiesi Clinical Trial - Site 70556

    Gradiska, Bosnia and Herzegovina

  • Chiesi Clinical Trial - Site 70560

    Mostar, Bosnia and Herzegovina

  • Chiesi Clinical Trial - Site 70562

    Mostar, Bosnia and Herzegovina

  • Chiesi Clinical Trial - Site 70559

    Sarajevo, Bosnia and Herzegovina

  • Chiesi Clinical Trial - Site 70561

    Sarajevo, Bosnia and Herzegovina

  • Chiesi Clinical Trial - Site 70551

    Travnik, Bosnia and Herzegovina

  • Chiesi Clinical Trial - Site 70558

    Trebinje, Bosnia and Herzegovina

420 more sites on the registry record.ClinicalTrials.gov ↗

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study — it may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
12 Jul 2021
Primary completion
23 Dec 2025
Completion
23 Dec 2025
Last update posted
2 Feb 2026
Registered enrollment
3,973
Registry id
NCT04636814

Cross-registrations

EU-CTR / CTIS (EudraCT)2023-510174-13-00EU-CTR / CTIS (EudraCT)2020-003648-97

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 12 Jul 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.