Study to Evaluate the Effectiveness of Legalon®

CompletedOBSERVATIONAL
Enrollment

362

Participants

Timeline

Start Date

August 8, 2022

Primary Completion Date

October 31, 2024

Study Completion Date

October 31, 2024

Conditions
Non-alcoholic Fatty Liver Disease (NAFLD)
Interventions
DRUG

Legalon® 140 mg

Legalon® 140 mg as per the Summary of Product Characteristics (SPC) and as per treating Investigator's decision

Trial Locations (1)

10400

Phramongkutklao Hospital, 315 Ratchawithi Rd, Thung Phaya Thai, Ratchathewi, Bangkok

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Meda Pharma S.p.A.

UNKNOWN

lead

Mylan Inc.

INDUSTRY