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Switching to TAF from NUCs Combination with Viral Suppression for Multiple Drug-Resistant Chronic Hepatitis B

Switching to TAF from NUCs Combination with Viral Suppression for Multiple Drug-Resistant Chronic Hepatitis B

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300068651
Enrollment
Unknown
Registered
2023-02-27
Start date
2023-02-27
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

Chronic Hepatitis B

Interventions

Multiple Drug-Resistant Chronic Hepatitis B with NUCs Combination treatment group:TAF

Sponsors

Third Hospital of Hebei Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Chronic HBV infected patients confirmed by liver biochemistry, serology, transient liver elastography, and/or liver pathology Male or female adult (age >18 years) Compensated liver function Treated with NUCs combination( ETV+ADV; ETV+TDF; LDT+ADV; LDT+TDF; LAM+ADV; LAM+TDF) HBV resistant HBV DNA < 69IU/ml ALT< 10 ULN Patient is able to give written informed consent prior to study start and to comply Medication compliance ranges from 80% to 120%.

Exclusion criteria

Exclusion criteria: Evidence of decompensated liver disease Evidence of primary hepatic carcinoma Coinfected with HCV or HIV Evidence of other autoimmune or metabolic liver diseases (except non-alcoholic fatty liver disease) Other malignant tumor(except those cured) Current abuse of illegal drugs or alcohol, sufficient in the investigator's opinion to prevent adequate compliance with study therapy or to increase the risk of hepatotoxicity or pancreatitis Women who are pregnant or breastfeeding Other serious medical conditions that might preclude completion of this study or that require chronic administration of prohibited medications Moribund state including advanced/pre-terminal liver cancer or other non-hepatic cancers

Design outcomes

Primary

MeasureTime frame
HBV-DNA;

Secondary

MeasureTime frame
ALT;HBsAg HBsAb HBeAg HBeAb HBcAb;creatinine;Ca;P;TC?TG?HDL?LDL;GLU;

Countries

China

Contacts

Public ContactNan Yuemin

the third hospital of Hebei medical university

nanyuemin@163.com+86 18533112266

Outcome results

None listed

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