A Study of ThermoDox™ in Combination With Radiofrequency Ablation (RFA) in Primary and Metastatic Tumors of the Liver

Completed · Phase 1

Conditions studied: Hepatocellular Carcinoma, Liver Neoplasms

In brief

The purpose of this study is to determine the maximum tolerated dose (MTD) of ThermoDox when used in combination with radiofrequency ablation (RFA) in the treatment of primary and metastatic tumors of the liver.

Key facts

Study ID

NCT00441376

Run by

Imunon

People needed

30

Starts

2007-02-01

Expected to finish

2009-12-01

Last updated by the study team

2019-02-07

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Be 18 years of age or older.
• Are willing to sign an informed consent form, indicating that they are aware of the investigational nature of this study that is in keeping with the policies of the institution.
• Have a diagnosis of metastatic liver cancer (MLC) or primary hepatocellular cancer (HCC) confined to the liver.
• Be an appropriate candidate for receiving RFA as a medically indicated treatment.
• Have an echocardiogram revealing an Ejection Fraction (EF) ≥ 50%.
• Willing to return to the study site for their imaging scans.
• Have life expectancy of ≥ 3 months.
• Have ECOG performance status of 0-2 or Karnofsky score of 60-100% (see Appendix II).
• Have no more than Childs-Pugh Class B liver disease.
• Subjects must have no prior doxorubicin exposure.
• No single lesion should be > 7 cm in maximum diameter.
• Subjects must agree to receive no other systemic therapy from the time of study enrollment until a minimum of 21 days after their ThermoDox infusion

You may not qualify if…

• Have serious medical illnesses including, but not limited to, congestive heart failure, myocardial infarction or cerebral vascular accident within the last six months, or life threatening cardiac arrhythmias.
• Are pregnant or breast feeding. In women of childbearing potential, a negative pregnancy test (serum) is required at baseline, 1 month and each 3 month follow-up visit.
• Are not practicing an acceptable form of birth control (i.e. diaphragm, cervical cap, condom, surgical sterility or birth control pills. Woman whose husband has undergone a vasectomy must use a second form of birth control).
• Have known serious allergic reactions (anaphylaxis) to any of the drugs or liposomal components or imaging agents to be used in this study.
• Have portal or hepatic vein invasion/thrombosis.
• Have PT or PTT > 1.5 times the institution's upper normal limit (UNL), except in subjects who are therapeutically anticoagulated for non-related medical conditions such as atrial fibrillation.
• Have platelet count > 75,000/mm3, absolute neutrophil count > 1500/mm3, or Hgb > 10 (unless the hemoglobin value has been stable, the subject is cardiovascularly stable, asymptomatic and judged able to withstand the RFA
• Have serum creatinine ≤ 2.0 mg/dl (or calculated CrCl ≤ 60mL/min).
• Have contraindications to receiving doxorubicin HCl.
• Are being treated with other investigational agents (within a minimum of 30 days or 5 half-lives of the investigational agent).
• Have other concurrent malignancy (subjects with benign or non aggressive malignant tumors-e.g.: squamous cell cancer of the skin-may be included), evidence of extrahepatic cancer from their primary malignancy, or ongoing, medically significant active infection.
• Documented HIV positive.
• NYHA class III or IV cardiovascular disease or LVEF < 50%.
• Evidence of hemachromatosis.
• Are on any of the medications listed in section 6.3, which could have an adverse effect when combined with the study drug, and who cannot stop the medication for the duration of the study and 30 days beyond the treatment.

Where it is running

• Northshore Hospital - Long Island Jewish Health System — Manhasset, New York, United States

Full record on ClinicalTrials.gov

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