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Terminated Phase 2 Interventional Results available

A Phase 2, Randomized Dose-ranging Study to Evaluate the Efficacy of Tralokinumab in Adults With Idiopathic Pulmonary Fibrosis

ClinicalTrials.gov ID: NCT01629667

Public ClinicalTrials.gov record NCT01629667. 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 4, 2026, 12:53 PM EDT

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

Brief summary

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

To study the safety and effectiveness of multiple-doses of tralokinumab on pulmonary function in adults with mild to moderate idiopathic pulmonary fibrosis (IPF). IPF is a chronic, progressive, irreversible, and usually fatal lung disease of unknown cause.

Study identification

NCT ID
NCT01629667
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
MedImmune LLC
Industry
Enrollment
409 participants

Conditions and interventions

Interventions

Biological · Other

Eligibility (public fields only)

Age range
50 Years to 79 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 30, 2012
Primary completion
Apr 30, 2015
Completion
Dec 31, 2015
Last update posted
May 14, 2017

2012 – 2016

United States locations

U.S. sites
21
U.S. states
17
U.S. cities
21
Facility City State ZIP Site status
Research Site Phoenix Arizona
Research Site La Jolla California
Research Site Sacramento California
Research Site Tampa Florida
Research Site Winter Park Florida
Research Site Atlanta Georgia
Research Site Honolulu Hawaii
Research Site Chicago Illinois
Research Site Louisville Kentucky
Research Site Ann Arbor Michigan
Research Site Rochester Minnesota
Research Site Chesterfield Missouri
Research Site Summit New Jersey
Research Site Durham North Carolina
Research Site Hershey Pennsylvania
Research Site Philadelphia Pennsylvania
Research Site Charleston South Carolina
Research Site Nashville Tennessee
Research Site McAllen Texas
Research Site McKinney Texas
Research Site Salt Lake City Utah

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 24 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01629667, 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 14, 2017 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01629667 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →