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Clinical Research of Licartin Combined With TACE in the Treatment of Unresectable Hepatocellular Carcinoma

N

Naval Military Medical University (Second Military Medical University)

Status and phase

Completed
Phase 4

Conditions

Unresectable Hepatocellular Carcinoma

Treatments

Procedure: Transcatheter arterial chemoembolization
Drug: Licartin

Study type

Interventional

Funder types

Other

Identifiers

NCT00829465
EHBH-RCT-2008-013

Details and patient eligibility

About

Liver cancer is a highly invasive malignancy and the rate of surgical resection is no more than 28%. After diagnosis, the average survival rate of patient is less than 50% in 6 month, less than 24% in 1 year and 5% in 5 year. The TACE treatment, under the theoretical basis of blood supply of Liver cancer, is obviously better than the other non-surgical therapy, in terms of tumor regression, AFP decrease, survival time and the evaluation of the quality of life. However, its overall effect is not yet satisfactory. As a result, concerning the research of drug for liver cancer and improving the overall efficacy of the treatment of liver cancer has a very real and important clinical significance and social value. Licartin (Iodine-131-Labeled Metuximab) injection is a antibody drug with new target and the only drug that China own the intellectual property rights. It has specific high affinity with HAb18G/CD147, the liver cell membrane antigen. Labeled 131I is taken to the liver tissue, owning high-dose concentration and releasing β particles to liver cancer cells to and kill cancer cells.

The Second Military Medical University, Eastern Hepatobiliary Surgery Hospital, planed to use the treatment of Licartin combined with TACE for the patients of unresectable hepatocellular carcinoma and evaluate the difference of tumor size, AFP change, TTP, the overall survival rate between different treatment group.

Full description

Liver cancer is a highly invasive malignancy and the rate of surgical resection is no more than 28%. The TACE treatment, under the theoretical basis of blood supply of Liver cancer, is obviously better than the other non-surgical therapy, in terms of tumor regression, AFP decrease, survival time and the evaluation of the quality of life. Licartin injection is a antibody drug with new target and the only drug that China own the intellectual property rights. It has specific high affinity with HAb18G/CD147, the liver cell membrane antigen. Labeled 131I is taken to the liver tissue, owning high-dose concentration and releasing β particles to liver cancer cells to and kill cancer cells.

The Second Military Medical University, Eastern Hepatobiliary Surgery Hospital, planed to use the treatment of Licartin combined with TACE for the patients of unresectable hepatocellular carcinoma and evaluate the difference of tumor size, AFP change, TTP, the overall survival rate between different treatment group.

Enrollment

400 patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. the participation is entirely voluntary, good at compliance, sign the informed consent form in person;
  2. diagnosed to be hepatocellular carcinoma by clinical method, imaging method and tumor markers; and the surgeons determine who can not undergo surgery;
  3. confirmed to recurrent after surgery by pathology;
  4. KPS score of physical state ≥ 60 points;
  5. liver function is Child-Pugh A or B class

Exclusion criteria

  1. General situation is poor and liver function Child-Pugh is C class;
  2. there is a serious heart, kidney and blood system diseases in patients;
  3. poor compliance;
  4. there is allergy history of biological agents or in a state of allergy;
  5. pregnancy and breast-feeding women

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

400 participants in 2 patient groups

control
Active Comparator group
Treatment:
Procedure: Transcatheter arterial chemoembolization
therapy
Experimental group
Treatment:
Drug: Licartin
Procedure: Transcatheter arterial chemoembolization

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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