A Phase II Study of an Anti-Tumor Immunotherapy Regimen Comprised of Pegylated Interferon-Alpha 2b and HyperAcute Melanoma Vaccine for Subjects With Advanced Melanoma

Status unconfirmed · Phase 2

Conditions studied: Melanoma

In brief

The purpose of this study is to determine the safety of giving subjects with advanced, recurrent or refractory melanoma the HyperAcute® Melanoma vaccine with a variant of a drug, called Interferon (PEG-Intron®) that is specially formulated to be given on a weekly basis (instead of daily). The study vaccine (HyperAcute®-Melanoma) is made from three types of human melanoma cell lines (grown in the laboratory) in which the genes have been slightly changed. This clinical study will try to discover the safety of the study vaccine combined with PEG-Intron®, its side effects and the potential benefits, if any.

Key facts

Study ID

NCT00746746

Run by

Ochsner Health System

People needed

30

Starts

2008-06-01

Expected to finish

2011-06-01

Last updated by the study team

2011-01-13

Who can join

Age: 19 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 19 years or older
• Histological diagnosis of melanoma
• AJCC Stage IIIC (any T, N1b, N2b, N3, M0) or Stage IV (any T, and N, M1), metastatic, progressive, refractory, recurrent or high risk of recurrence melanoma.
• Expected survival of more than 6 months
• Adequate organ function
• Measurable or non-measurable disease
• Must have negative serologies for Hepatitis B and C and HIV prior to entering study
• Must be more than 4 weeks since major surgery, radiotherapy, chemotherapy or biotherapy/targeted therapies
• Male and female subjects of child producing potential must agree to use contraception or avoidance pregnancy measures while enrolled on the study and for one month after the last immunization.

You may not qualify if…

• Active CNS metastases or carcinomatous meningitis
• Hypercalcemia
• Pregnant or nursing women
• Other malignancy within five years
• History of organ transplant or current active immunosuppressive therapy
• Subjects taking systemic corticosteroid therapy
• Active infection or antibiotics within 1-week prior to study
• Uncontrolled or significant congestive heart failure, myocardial infarction, ventricular arrhythmias or pulmonary dysfunction
• Autoimmune disease
• A known allergy to any component of the HyperAcute vaccine or PEG-Intron
• Patients having undergone splenectomy
• Patients with sickle-cell anemia or thalassemia major.

Where it is running

• Ochsner Health System — New Orleans, Louisiana, United States

Full record on ClinicalTrials.gov

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