CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 160 enrolled
Drug / intervention
Pamrevlumab +3 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01890265
NCT01890265Phase 2Completed

A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety and Efficacy of FG-3019 in Patients With Idiopathic Pulmonary Fibrosis

Kyntra Bio·interventional·Posted Jul 1, 2013·Updated Sep 4, 2020

In Brief

A Phase 2 clinical trial evaluating Pamrevlumab, Placebo, and 2 other interventions for Idiopathic Pulmonary Fibrosis. Completed, enrolled 160 participants across 42 sites in 7 countries.

Detailed Summary

To evaluate the safety and tolerability of pamrevlumab in participants with IPF, and the efficacy of pamrevlumab in slowing the loss of forced vital capacity (FVC) and the progression of IPF in these participants.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustralia, Bulgaria, Canada, India, New Zealand, South Africa, United States
Collaborators--

Timeline

Phase 2CompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedJul 1, 2013
Enrollment StartJul 30, 2013
Primary CompletionNov 16, 2017
TodayJul 2, 2026
Enrollment to primary: 4.3 yearsPosted 13.0 years ago

Interventions

Pamrevlumabdrug

Solution for infusion

Placebodrug

Solution for infusion

Sub-Study: Pirfenidonedrug

Pirfenidone concomitant therapy will not be provided by the Sponsor.

Sub-Study: Nintedanibdrug

Nintedanib concomitant therapy will not be provided by the Sponsor.