Leronlimab (PRO 140) in Patients With Nonalcoholic Steatohepatitis

PHASE2CompletedINTERVENTIONAL
Enrollment

87

Participants

Timeline

Start Date

December 1, 2020

Primary Completion Date

December 29, 2021

Study Completion Date

December 29, 2021

Conditions
Nonalcoholic Steatohepatitis (NASH)
Interventions
DRUG

Placebo

Placebo will be administered subcutaneously every week for 13 weeks.

DRUG

leronlimab 700 mg

700 mg leronlimab will be administered subcutaneously every week for 13 weeks.

DRUG

leronlimab 350 mg

350 mg leronlimab will be administered subcutaneously every week for 13 weeks.

Trial Locations (7)

30501

Center for Advanced Research & Education, Gainesville

32751

Meridien Research, Maitland

33016

Floridian Clinical Research, Miami Lakes

34761

Sensible Healthcare, LLC, Ocoee

75126

Care United Research LLC, Forney

78215

American Research Corporation, San Antonio

92118

Southern California Research Center, Coronado

Sponsors

Lead Sponsor

All Listed Sponsors
lead

CytoDyn, Inc.

INDUSTRY

NCT04521114 - Leronlimab (PRO 140) in Patients With Nonalcoholic Steatohepatitis | Biotech Hunter | Biotech Hunter