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NCT05178303CompletedPhase 4

Composition for Treating Cirrhosis and Liver Cancer (SB-1121)

Composition for Treating Cirrhosis and Liver Cancer

Source: ClinicalTrials.gov · Last updated 6 Nov 2026

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Brief summary (registry, in English)

The composition treats cirrhosis and hepatocellular carcinoma (Hcc) at an early stage. The product is extracted from herbs, including Adenosma glutinosum extract, Eclipta prostrata extract, Phyllanthus urinaria extract, Impatiens balsamina extract, Ascorbic acid, pyridoxine 5-phosphate, L-Arginine hydrochloride, Pregnenolone acetate. These components have participated in repairing and regenerating new liver parenchyma, preventing fibrosis cell generation, preventing liver cancer cell growth at an early stage. The composition supplements precursors which help the body strengthen antibodies and reduce the risk of inflammation, restore physiological and biochemical functions of liver cells after chronic inflammation.

Status (registry)
Completed
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
24 (actual)
First submitted
1 Dec 2021
Start date
30 Nov 2015
Primary completion date
10 Oct 2025
Lead sponsor
Nguyen Thi Trieu, MD
NCT number
NCT05178303

What you commit to

  • Study type: Interventional · Phase 4
  • Participants enrolled: 24
  • From 30 Nov 2015 to the primary completion date, 10 Oct 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Unstable cancer patients.

Other

  • Decompensated cirrhosis.

Who the study is looking for

  • All patients with underlying medical conditions who have been taking medications for these conditions.
  • Patients with AIDS, HIV, HBV, HCV, and patients with co-infections.
  • The cancer patients are stable.
  • Patients with congenital or acquired immunodeficiency.

Age in the registry: 18 years to 80 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Saigon Biopharma Company LimitedHo Chi Minh CityVietnamUnknown status

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This page is information, not medical advice. Discuss any trial with your doctor.