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A 12-week, Multicenter, Randomized, Double-blind, Placebo-Controlled Clinical Trial for the Evaluation of the Efficacy and Safety of KBL982 on Improving Alcoholic Liver Dysfunction

A 12-week, Multicenter, Randomized, Double-blind, Placebo-Controlled Clinical Trial for the Evaluation of the Efficacy and Safety of KBL982 on Improving Alcoholic Liver Dysfunction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0006987
Enrollment
105
Registered
2022-02-09
Start date
2021-11-05
Completion date
Unknown
Last updated
2025-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Dietary Supplement : - KBL982: twice a day - Placebo: twice a day

Sponsors

Kobiolabs
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Males and females aged over 19 years, under 75 years at the screening examination 2) Participants who have fully understand the information provided about the study voluntarily decided to participate and agree to comply with precautions

Exclusion criteria

Exclusion criteria: 1) Patients with cirrhosis or liver cancer according to abdominal ultrasonography based on visit 2 2) Those who have received chemotherapy or are being treated for malignant tumors other than basal cell carcinoma and squamous cell carcinoma (restrained non-invasive lesions) or those who have been cured of cancer for less than 5 years. 3) In Visit 1, a positive factor for HBs Ag or HCV Ab test. 4) Uncontrolled thyroid disease patients. 5) A person who complains of severe gastrointestinal symptoms such as heartburn and indigestion and has a problem in eating food for human application tests. 6) Those who are sensitive or allergic to food ingredients for this human application test. 7) A person who is pregnant or has plans to become pregnant during the human body application test. 8) Those who participated in other interventional clinical trials (including human application trials) within 1 month of visit 1, or who plan to participate in other interventional clinical trials (including human application trials) after the start of this human application trial. 9) A person who determines that the tester is inappropriate for this human body application test.

Design outcomes

Primary

MeasureTime frame
Gamma-Glutamyl Transferase

Secondary

MeasureTime frame
Aspartate Aminotransferase, Alanine Transaminase

Countries

Korea, Republic of

Contacts

Public ContactWoolim Jung

Neonutra

123dnfla@neonutra.com+82-70-7722-4034

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026