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Clinical Trial Summary

A randomized, controlled pilot trial to evaluate the efficacy and safety of subcutaneous Abatacept in treating interstitial lung disease associated with the anti-synthetase syndrome.


Clinical Trial Description

This is a proof of concept study to evaluate the efficacy, safety and tolerability of abatacept in Syn-ILD in a multi-center randomized, placebo-controlled 6-month (24-week) pilot study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03215927
Study type Interventional
Source University of Pittsburgh
Contact
Status Active, not recruiting
Phase Phase 2
Start date June 1, 2017
Completion date July 30, 2023

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