ClinicalTrials.gov record
Terminated Phase 3 Interventional

Extension Trial on Efficacy / Safety of L-CsA + SoC in Treating BOS in Post Single or Double Lung Transplant (BOSTON-3)

ClinicalTrials.gov ID: NCT04039347

Public ClinicalTrials.gov record NCT04039347. 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 May 20, 2026, 11:44 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

A Phase III, Extension Clinical Trial to Demonstrate Efficacy and Safety of Liposomal Cyclosprine A Via the PARI Investigational eFlow® Device and SoC in Treating Bronchiolitis Obliterans in Patients Post Single or Double Lung Transplant

Study identification

NCT ID
NCT04039347
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Zambon SpA
Industry
Enrollment
164 participants

Conditions and interventions

Interventions

  • Liposomal Cyclosporine A 10 mg Drug
  • Liposomal Cyclosporine A 5 mg Drug

Drug

Eligibility (public fields only)

Age range
18 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
Mar 11, 2020
Primary completion
Feb 24, 2026
Completion
Feb 24, 2026
Last update posted
Apr 6, 2026

2020 – 2026

United States locations

U.S. sites
20
U.S. states
12
U.S. cities
17
Facility City State ZIP Site status
Banner - University Medical Center Phoenix Arizona 85006
David Geffen School of Medicine at UCLA Los Angeles California 90095
UCSF San Francisco California 94143
UCSF Center for Advanced Lung Disease Stanford California 94305
University of Florida Dept of Pulmonary Medicine Gainesville Florida 32610
Indiana University Indianapolis Indiana 46202
UK Albert B. Chandler Hospital Lexington Kentucky 40508
University of Maryland Baltimore Maryland 21201
Johns Hopkins University Hospital Baltimore Maryland 21287
Barnes-Jewish Hospital St Louis Missouri 63110
Columbia University Medical Center New York New York 10032
Duke University Durham North Carolina 27710
Cleveland Clinic Cleveland Ohio 44195
OSU Wexner Medical Center Columbus Ohio 43210
Temple University Hospital Philadelphia Pennsylvania 19140
University of Pittsburgh Medical Center Pittsburgh Pennsylvania 15232
Baylor University Medical Center Dallas Texas 75246
University of Texas Southwestern Medical Center Dallas Texas 75390
Baylor College of Medicine Houston Texas 77030
Houston Methodist Hospital Houston Texas 77030

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 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04039347, 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 Apr 6, 2026 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04039347 live on ClinicalTrials.gov.

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