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Clinical Trials/NCT00116363
NCT00116363
Unknown
Phase 2

Phase II Study Examining the Biological Efficacy of Intratumoral INGN 241 (Ad-mda7) Administration in Patients With In Transit Melanoma

Introgen Therapeutics1 site in 1 country25 target enrollmentMarch 2005

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Malignant Melanoma
Sponsor
Introgen Therapeutics
Enrollment
25
Locations
1
Primary Endpoint
anti-tumor effects and systemic immune activation at 28 days
Last Updated
18 years ago

Overview

Brief Summary

This is a research study to look at the ways in which a treatment called INGN241 can kill melanoma cells or help the patient's immune system kill melanoma cells.

Detailed Description

INGN 241 is an adenoviral vector carrying the MDA-7 cDNA. MDA-7 is a novel tumor suppressor molecule with cytokine properties, recently designated as IL-24. Over expression of MDA-7 in melanoma cells in vitro has been shown to inhibit cellular proliferation and induce apoptosis. Loss of MDA-7 expression in human melanomas has been shown to correlate with invasion and metastasis. The INGN 241 gene transfer construct has been previously used in human subjects in an ongoing open label Phase I study using intratumoral administration, and has been well tolerated to date. The primary objectives of the present study are to determine if INGN 241, injected into a melanoma in transit lesion, can induce apoptosis in regional uninjected lesions and initiate systemic immune activation. Secondary objectives include examination of specific immunity and of clinical response and toxicity.

Registry
clinicaltrials.gov
Start Date
March 2005
End Date
December 2006
Last Updated
18 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Introgen Therapeutics

Eligibility Criteria

Inclusion Criteria

  • Histologically proven melanoma, must have 3 regional metastatic lesions that are in transit

Exclusion Criteria

  • Central nervous system involvement by melanoma

Outcomes

Primary Outcomes

anti-tumor effects and systemic immune activation at 28 days

Secondary Outcomes

  • tumor response
  • toxicity and safety
  • the induction of antigen-specific T-lymphocytes after multiple cycles of treatment

Study Sites (1)

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