31
Participants
Start Date
January 3, 2018
Primary Completion Date
January 31, 2020
Study Completion Date
January 31, 2020
Valganciclovir
Subjects with IPF currently tolerating pirfenidone treatment who have evidence of prior EBV or CMV infection will be randomized to valganciclovir or placebo for 12 weeks.
Placebo
Subjects with IPF currently tolerating pirfenidone treatment who have evidence of prior EBV or CMV infection will be randomized to valganciclovir or placebo for 12 weeks.
Vanderbilt University Medical Center, Nashville
Collaborators (1)
Genentech, Inc.
INDUSTRY
Vanderbilt University Medical Center
OTHER