41
Participants
Start Date
June 22, 2021
Primary Completion Date
February 13, 2025
Study Completion Date
February 13, 2025
CVL-871 1.0 mg
CVL-871 1.0 mg, oral (tablet), once per day for 12 weeks (stepped up-titration of dose days 1-7)
CVL-871 3.0 mg
CVL-871 3.0 mg QD oral (tablet), once per day for 12 weeks (stepped up-titration of dose days 1-21)
Placebo
Placebo QD, oral (tablet), once per day for 12 weeks
Staten Island, New York, Staten Island
Abington, Pennsylvania, Abington
Fairfax, Virginia, Fairfax
Charleston, South Carolina, Charleston
Decatur, Georgia, Decatur
Orlando, Florida, Orlando
Miami, Florida, Miami
Miami, Florida, Miami
Wellington, Florida, Wellington
Delray Beach, Florida, Delray Beach
Columbus, Ohio, Columbus
Little Rock, Arkansas, Little Rock
Scottsdale, Arizona, Scottsdale
San Diego, California, San Diego
Santa Ana, California, Santa Ana
New Haven, Connecticut, New Haven
Plymouth, Massachusetts, Plymouth
Calgary, Alberta, Calgary
Victoria, British Columbia, Victoria
Toronto, Ontario, Toronto
Lead Sponsor
AbbVie
INDUSTRY