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