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Terminated Phase 3 Interventional Results available

Zephyrus II: Efficacy and Safety Study of Pamrevlumab in Participants With Idiopathic Pulmonary Fibrosis (IPF)

ClinicalTrials.gov ID: NCT04419558

Public ClinicalTrials.gov record NCT04419558. 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 Jul 21, 2026, 6:56 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

Zephyrus II: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Efficacy and Safety Study of Pamrevlumab in Subjects With Idiopathic Pulmonary Fibrosis (IPF)

Study identification

NCT ID
NCT04419558
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Kyntra Bio
Industry
Enrollment
372 participants

Conditions and interventions

Interventions

  • Pamrevlumab Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
40 Years to 85 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
Sep 29, 2020
Primary completion
Sep 3, 2023
Completion
Sep 3, 2023
Last update posted
Aug 11, 2024

2020 – 2023

United States locations

U.S. sites
23
U.S. states
18
U.S. cities
23
Facility City State ZIP Site status
UAB Lung Health Center Birmingham Alabama 35294
UC San Francisco San Francisco California 94143
National Jewish Health Denver Colorado 80206
Yale University New Haven Connecticut 06520
St. Francis Medical Center Clearwater Florida 33765
Pulmonary Disease Specialists d/b/a PDS Research Kissimmee Florida 34741
TGH/USF Center for Advanced Lung Disease and Lung Transplant Tampa Florida 33606
Emory University/The Emory Clinic Atlanta Georgia 30324
University of Iowa Iowa City Iowa 52242
The University of Kansas Medical Center Kansas City Kansas 66160
University of Maryland Medical Center Baltimore Maryland 21201
The General Hospital Corporation d/b/a Massachusetts General Hospital Boston Massachusetts 02114
Spectrum Health Grand Rapids Michigan 49504
University of Minnesota Minneapolis Minnesota 55455
Mayo Clinic Rochester Minnesota 55905
Duke University Medical Center Durham North Carolina 27710
PulmonIx, LLC Greensboro North Carolina 27403
Ohio State University Columbus Ohio 43221
Penn State Milton S Hershey Medical Center Hershey Pennsylvania 17033
University of Pennsylvania Philadelphia Pennsylvania 19104
Low Country Lung and Critical Care, PA Charleston South Carolina 29406
The University of Vermont Burlington Vermont 05405
University of Wisconsin Clinical Research Madison Wisconsin 53706

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 134 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04419558, 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 Aug 11, 2024 · Synced Jul 21, 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 protocol, eligibility criteria, and contact information for NCT04419558 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →