Basic Trial Information
Trial Description
     Summary
     Eligibility Criteria
Trial Contact Information

Basic Trial Information

Phase	Type	Status	Age	Sponsor	Protocol IDs
Phase III	Treatment	Approved-not yet active	18 to 90	Pharmaceutical / Industry	CA033 NCT00864253

Trial Description

Summary

The main purpose of this research study is to compare the safety, tolerability, and anti tumor activity of an investigational drug, ABI-007 versus Dacarbazine in patients with metastatic melanoma who have not previously received chemotherapy. ABI-007 is a new preparation of the active drug paclitaxel. It contains the same medication as the prescription chemotherapy drug Abraxane®. Abraxane® is approved by the FDA for the treatment of metastatic breast cancer after failure of combination chemotherapy for metastatic disease or relapse within 6 months of adjuvant chemotherapy.

Dacarbazine is approved by the FDA for the treatment of melanoma. In this study, ABI-007 and Dacarbazine will be tested as therapy for people who have not yet had any cancer treatment for the diagnosis of metastatic melanoma.

Eligibility Criteria

Inclusion Criteria:

• Histologically or cytologically confirmed malignant melanoma with evidence of metastasis (Stage IV).

• No prior cytotoxic chemotherapy for metastatic malignant melanoma is permitted. Prior treatment with kinase inhibitors or cytokines is permitted.

• No prior adjuvant cytotoxic chemotherapy is permitted. Prior adjuvant therapy with interferon, GM-CSF and/or vaccines is permitted.

• Male or non-pregnant and non-lactating female, and ≥ 18 years of age. If a female patient is of child-bearing potential, as evidenced by regular menstrual periods, she must have a negative serum pregnancy test (ß-hCG) within 72 hours prior to first study drug administration. If sexually active, the patient must agree to utilize contraception considered adequate and appropriate by the investigator.

• No other current active malignancy within the past 3 years.

• Radiographically-documented measurable disease (defined by the presence of at least 1 radiographically documented measurable lesion [see Section 8.3.1.1 for definition of measurable lesions]).

• Patient has the following blood counts at Baseline:

• ANC ≥ 1.5 x 109 cells/L;

• platelets ≥ 100 x 109 cells/L;

• Hgb ≥ 9 g/dL.

• Patient has the following blood chemistry levels at Baseline:

• AST (SGOT), ALT (SGPT) ≤ 2.5x upper limit of normal range (ULN); ≤ 5.0 xULN if hepatic metastases present;

• total bilirubin ≤ ULN;

• creatinine ≤ 1.5 mg/dL.

• LDH ≤ 2.0 x ULNa

• Expected survival of > 12 weeks.

• ECOG performance status 0-1.

• Patient or his/her legally authorized representative or guardian has been informed about the nature of the study, and has agreed to participate in the study, and signed the Informed Consent form prior to participation in any study-related activities.

Exclusion Criteria:

• History of or current evidence of brain metastases, including leptomeningeal involvement.

• Patient has pre-existing peripheral neuropathy of NCI CTCAE Scale of Grade ≥ 2.

• Prior radiation to a target lesion is permitted only if there has been clear progression of the lesion since radiation was completed.

• Patient has a clinically significant concurrent illness.

• Patient is, in the investigator's opinion, unlikely to be able to complete the study through the End of Study (EOS) visit.

• Patient is currently enrolled, or will enroll in a different clinical study in which investigational therapeutic procedures are performed or investigational therapies are administered while participating in this study. Marker studies or studies evaluating biological correlates are permitted.

• Patient has serious medical risk factors involving any of the major organ systems such that the investigator considers it unsafe for the patient to receive an experimental research drug.

Trial Contact Information

Trial Lead Organizations/Sponsors

Abraxis Oncology

Evan M. Hersh

Principal Investigator

Michael Millward

Principal Investigator

José Iglesias, MD

Study Director

Evan Hersh, MD		Ph: 520-694-9062
		Email: hnichols@azcc.arizona.edu

Heather Nichols, RN		Ph: 520-694-9062
		Email: hnichols@azcc.arizona.edu

Link to the current ClinicalTrials.gov record.
NLM Identifer NCT00864253
Information obtained from ClinicalTrials.gov on May 13, 2009