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OpenTrials
Completed

NCT Number: NCT01052142

Safety Study of a Liposomal Vaccine to Treat Malignant Melanoma

The purpose of this study is to determine whether Lipovaxin-MM, a new anti-cancer vaccine, is safe and effective in improving the body's ability to destroy cancer cells in patients with metastatic melanoma.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Pain & Anaesthesia Research Clinic

Adelaide, South Australia, 5000, Australia

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Key Inclusion Criteria:

  • Patients with incurable stage IV malignant melanoma for which no standard or curative therapy exist OR patients locoregionally recurrent melanoma (including local metastases, in transit metastases and satellitosis) where surgery is not the best therapeutic option.
  • Must be able and willing to provide written informed consent.
  • Eastern Cooperative Oncology Group Performance Status of 0 or 1.
  • Life expectancy of ≥12 weeks.
  • Female subjects must be of non-child-bearing potential or using appropriate contraception.
  • Positive test for cell mediated immunity.

Key Exclusion Criteria:

  • Brain metastases or spinal cord compression, unless treatment was completed at least 4 weeks before entry and stable without steroid treatment for at least 4 weeks.
  • Previous immunotherapy (except IL-2 or interferon-based therapy) for melanoma.
  • Inadequate bone marrow reserve.
  • Serum bilirubin ≥1.2 times the upper limit of normal.
  • In absence of metastases, liver transaminase levels greater than 1.5 times the upper limit of normal.
  • If metastases are evident, liver transaminase levels 2.5 times the upper limit of normal will be acceptable.
  • Inadequate renal function.
  • Evidence of severe or uncontrolled systemic diseases.
  • Unresolved toxicity ≥CTC Grade 2 from previous anti-cancer therapy except alopecia (if applicable) unless agreed that the patient can be entered after discussion with the Medical Monitor.
  • Participation in a trial of an investigational agent within the prior 30 days.
  • HIV infection.
  • Immunosuppressive therapy including corticosteroids within 4 weeks of screening.
  • Pregnant or breast-feeding females.

Treatment and study plan

Lipovaxin-MM

Biological

Patients will receive three doses of Lipovaxin-MM by intravenous infusion at intervals of four weeks OR patients will receive 4 doses of Lipovaxin-MM by intravenous infusion at weekly intervals

Primary outcomes

  1. Adverse events

    Time frame: Within 84 days after first dose

  2. Immunogenicity

    Time frame: Within 42 days of first dose

    antigen specific immune responses will be monitored

Secondary outcomes

  1. Anti-cancer activity (RECIST criteria)

    Time frame: Within 84 days of first dose

    assessed every 6 weeks of study

Sponsors and collaborators

Lead sponsor

Lipotek Pty Ltd

Industry

Collaborators

  • Royal Adelaide Hospital
  • Trident Clinical Research Pty Ltd

Registry information

Official study title

A Phase I Open-label Study of the Safety and Immunogenicity of Escalating Doses of Lipovaxin-MM, a Novel Melanoma Immunotherapeutic, in Patients With Metastatic Melanoma

Important dates

Study start
2009
Primary completion
2012
Study completion
2012
First posted
Jan 20, 2010
Registry last updated
Apr 11, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.