A Study to Assess the Efficacy and Safety of Namilumab in Participants With Chronic Pulmonary Sarcoidosis
Status: Recruiting
Conditions: Sarcoidosis
Location:
Kinevant Study SiteCity/State:
Birmingham, Alabama
Palo Alto, California
Valencia, California
Denver, Colorado
Gainesville, Florida
Augusta, Georgia
Chicago, Illinois
Iowa City, Iowa
Kansas City, Kansas
New Orleans, Louisiana
Baltimore, Maryland
Minneapolis, Minnesota
Rochester, Minnesota
Greenville, North Carolina
Cincinnati, Ohio
Cleveland, Ohio
Philadelphia, Pennsylvania
Pittsburgh, Pennsylvania
Charleston, South Carolina
Rock Hill, South Carolina
Dallas, Texas
Houston, Texas
Charlottesville, Virginia
Falls Church, Virginia
Contact Information:
Gary Barrera
650-303-7132
[email protected]
This is a randomized, double-blind, placebo-controlled study with an OLE.
Participants will be randomized to receive namilumab or placebo in the 26-week Double-blind Treatment Period of the study. Namilumab, or placebo, will be administered subcutaneously (SC) every 4 weeks through Week 22 after the initial dosing period.
All participants, who complete the 26-week Double-blind Treatment Period, may be eligible to participate in the 28-week OLE.
Further details are in the protocol.
