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Clinical Program of Licartin Combined with ADV-TK for Prevention of Hepatocellular Carcinoma Recurrence after Liver Transplantation

Clinical Program of Licartin Combined with ADV-TK for Prevention of Hepatocellular Carcinoma Recurrence after Liver Transplantation

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-09000387
Enrollment
Unknown
Registered
2009-04-23
Start date
2009-05-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Hepatocellular carcinoma

Interventions

Group B:Conventional therapy after liver transplantation+ first therapy of intravenous injection with Licartin at the first weekend, the third weekend, sixth weekend of post-liver transplantation, tot
Group D:Control group: conventional therapy after liver transplantation and receive placebo at the time of therapy.
Group C:Injection of ADV-TK into peritoneum tissues around the liver during the liver transplantation operation and at week 3 and week 5 of post-operation.Intravenous injections of Licartin after each
Group A:Injection of ADV-TK into peritoneum tissues around the liver during the liver transplantation operation. The second and third injections of ADV-TK were administerted at week 3 and week 5 of po

Sponsors

Fourth Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients are entirely voluntary, good compliance, sign the informed consent form; 2. Age between 18 to 70 years old; 3. Tumor size exceeds the Milan criteria, but without extra-liver organ metastasis and large blood vessel invasion; 4. Disgnosis of hepatocellular carcinoma after surgery by pathology; 5. Without surgical contraindication to liver transplant operation.

Exclusion criteria

Exclusion criteria: 1. Allergic reactions to adenovirus, Ganciclovir, or the same kinds of biological agents; 2. Allergic reactions to biological agents, hypersensitiveness; 3. Poor compliance.

Design outcomes

Primary

MeasureTime frame
No recurrence survival time or (and) No progress survival;Overall survival time;Recurrence rate;One-year survival rate;

Secondary

MeasureTime frame
Recurrence rate;

Countries

China

Contacts

Public ContactZhi-Nan Chen
znchen@fmmu.edu.cn+86 029 84773243

Outcome results

None listed

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