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Status:

COMPLETED

Intralesional PV-10 Chemoablation of Metastatic Melanoma

Lead Sponsor:

Provectus Pharmaceuticals

Conditions:

Melanoma

Eligibility:

All Genders

18-85 years

Phase:

PHASE1

Brief Summary

The objective of this study is to investigate the safety of intralesional (IL) PV-10 for the treatment of metastatic melanoma. This study will also include a preliminary assessment of response of trea...

Detailed Description

This is a two center, open label, ascending dose study. Subjects with at least two measurable melanoma lesions will receive a single intralesional injection of 10% PV-10 solution into each of one to t...

Eligibility Criteria

Inclusion

  • Histologically or cytologically confirmed metastatic melanoma, American Joint Committee on Cancer (AJCC) Stage III (regional lymph node metastasis, in-transit metastasis or satellite metastasis) or Stage IV (distant metastasis)
  • Measurable disease in at least two lesions, each lesion ≤ 6 cm in diameter
  • Performance status: ECOG 0-2
  • Life expectancy: at least 6 months
  • Hematopoietic:
  • White blood cell count (WBC) at least 3000/mm3
  • Absolute neutrophil count (ANC) at least 1.5 (1,500/mm3)
  • Platelet count at least 100,000/mm3
  • Renal function:
  • Creatinine ≤ 2.0 mg/dL
  • Hepatic function:
  • Bilirubin ≤ 2.0 mg/dL
  • AST/ALT ≤ 3 times the upper limit of normal (ULN)
  • Cardiovascular function:
  • No major cardiovascular disease
  • Thyroid function:
  • T3 (serum triiodothyronine), T4 (serum thyroxine) and THS (serum thyrotropin) within normal limits
  • Immunological function:
  • Adequate immune system function in the opinion of the investigator

Exclusion

  • Radiation therapy within 4 weeks or to any study lesion within 12 weeks
  • Chemotherapy or other systemic cancer therapy within 4 weeks (6 weeks for nitrosoureas or mitomycin) or regional chemotherapy (limb infusion or perfusion) within 12 weeks
  • Local treatment (e.g., surgery, cryotherapy, radiofrequency ablation) to the treatment area within 4 weeks
  • Investigational agents within 4 weeks (or 5 half-lives)
  • Anti-tumor vaccine therapy within 12 weeks
  • Concurrent illness:
  • Severe diabetes or extremity complications due to diabetes
  • Significant concurrent disease or illness, psychiatric disorders, or alcohol or chemical dependence that would, in the opinion of the investigator, compromise subject safety or compliance or interfere with interpretation of study results
  • Thyroid autoregulatory dysfunction, including thyroid disease (subclinical or ongoing), goiter, partial thyroidectomy, prior radioiodine- or surgically-treated Graves' hyperthyroidism, or cystic fibrosis
  • Pregnancy or fertile female subjects who are not using effective contraception
  • Concurrent medications:
  • Subjects taking medications with a significant risk of photosensitization, such as thiazides, within one week (or 5 half-lives) of study treatment.

Key Trial Info

Start Date :

August 1 2005

Trial Type :

INTERVENTIONAL

End Date :

August 1 2007

Estimated Enrollment :

20 Patients enrolled

Trial Details

Trial ID

NCT00219843

Start Date

August 1 2005

End Date

August 1 2007

Last Update

August 23 2007

Active Locations (2)

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Page 1 of 1 (2 locations)

1

Sydney Melanoma Unit

North Sydney, New South Wales, Australia, 2060

2

Newcastle Melanoma Unit

Waratah, New South Wales, Australia, 2298