Phase III Study of PI-88 in Post-resection Hepatocellular Carcinoma (PATHWAY)

Progen Pharmaceuticals

Status and phase

Terminated

Phase 3

Conditions

Primary Liver Cancer

Hepatocellular Carcinoma

Cancer

Liver Cancer

Hepatoma

Treatments

Drug: placebo

Drug: PI-88

Study type

Interventional

Funder types

Industry

Identifiers

NCT00568308

PR88302

Details and patient eligibility

About

The purpose of this study is to determine if PI-88 is effective and safe in patients who have had surgery to remove primary liver cancer.

Full description

Primary liver cancer (hepatocellular carcinoma or HCC) is the fifth most common cancer worldwide. Surgery to remove the tumour remains the principal form of treatment for liver cancer, however recurrence of the disease after surgery is common and survival after recurrence is poor. At the moment there is no recommended standard treatment for HCC immediately after the tumour has been removed surgically. PI-88 is a new experimental drug which blocks the growth of new blood vessels in tumours to stop the tumour growing (starves it of food) and also stops tumour cells spreading. Previous experience with PI-88 has shown it has been well tolerated and has shown some benefit in delaying the time it takes for the hepatocellular carcinoma to reappear after surgery. The purpose of this study is to determine if PI-88 is effective and safe in patients who have had surgery to remove primary liver cancer.

Enrollment

600 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Key Inclusion Criteria:

Histologically-proven primary hepatocellular carcinoma with curative resection performed in the 4 - 6 weeks prior to randomisation.
ECOG performance status 0 to 2
Child Pugh classification A or B

Key Exclusion Criteria:

Any evidence of tumour metastasis or co-existing malignant disease
Any prior recurrence of HCC or any liver resection prior to the most recent procedure
History of prior HCC therapy