120
Participants
Start Date
June 1, 2025
Primary Completion Date
April 1, 2028
Study Completion Date
August 14, 2028
Maraviroc
Product will be administered for 300 mg immediately preceding the lung transplant surgery and then will be administered every 12 hours. There will be 7 total doses. The first 3 will be 300 mg doses and the remaining 4 will be 150 mg doses. Maraviroc will be given oral (PO) or by feeding tube (PFT) in crushed format depending on the route availability.
Placebo
Placebo in 300 and 150 mg formulations Product will be administered every 12 hours for 3 days. The placebo will be matched in appearance and taste to the Maraviroc and is available in PO and liquid (PFT) formulations.
University of California, San Francisco, San Francisco
National Heart, Lung, and Blood Institute (NHLBI)
NIH
University of California, San Francisco
OTHER