Could a flavonoid combo reverse liver scarring and prevent cancer in hepatitis b?
NCT ID NCT07084948
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This completed phase 4 trial tested whether adding SB Flavon (a blend of flavonoids, vitamin C, and L-arginine) to standard Tenofovir therapy can reverse advanced liver scarring (cirrhosis) and prevent liver cancer in 134 people with chronic hepatitis B. The study measured liver stiffness and cancer development over time. While the approach is promising, the results need confirmation in larger trials.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- SB Flavon (a blend of flavonoids, ascorbic acid, and L-arginine) plus Tenofovir
- What this could lead to
- If successful, this combination could help reverse advanced liver scarring and lower the risk of liver cancer in people with chronic hepatitis B.
- What could go wrong
- This is a single completed phase 4 trial with 134 participants. The results may not apply to all patients, and the supplement-like nature of SB Flavon means larger, more rigorous studies are needed to confirm benefits.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
134 people
The number who actually took part.
- Started
-
Nov 2015
- Finished
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Apr 2026
- Lead sponsor
-
An individual researcher
The lead sponsor is a named person rather than an organisation.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 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. Exclusion Criteria: * Unstable cancer patients. * Decompensated cirrhosis.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Saigon Biopharma Company Limited
Hồ Chí Minh, Ho Chi Minh City, 700000, Vietnam
-
Saigon Biopharma LLC
Wilmington, Delaware, 19801-6601, United States
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