Last updated on September 2016

Study to Evaluate the Safety and Tolerability of GBT440 Administered to Subjects With IPF

Brief description of study

This study is a randomized, double-blind, placebo-controlled trial in which eligible IPF subjects will be randomized to receive GBT440 or Placebo orally daily.

Clinical Study Identifier: NCT02846324

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Tatiana Blue

New York, NY United States
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Lisa Weaver

Salt Lake City, UT United States
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Marla Watson

Kansas City, KS United States
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Ashley Warden

Charleston, SC United States
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Cori Fratelli

Denver, CO United States
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Sharonda Keazor

Birmingham, AL United States
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Edwinia Battle

Falls Church, VA United States
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Francine McGonagle

Philadelphia, PA United States
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Sandy Ditta

New Orleans, LA United States
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Recruitment Status: Open

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