Melanoma Clinical Trial

Study of Temzolomide and Gleevec in Advanced Melanoma

Summary

This study has been designed to evaluate the side effects of Gleevec when given in combination with Temzolomide; and to learn more about how these drugs work in the body and whether this combination is useful in treating patients with melanoma.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Histologically confirmed melanoma that is metastatic or unresectable and for which standard curative or palliative measures do not exist or are no longer effective
Prior chemotherapy, immunotherapy, radiation therapy (Phase I portion only), cytokine, biologic, or vaccine therapy is permitted, however no prior treatment with temozolomide
Measurable disease
Performance status <= 2
Life expectancy greater than 3 months

Exclusion Criteria:

No prior treatment with temozolomide or imatinib mesylate
Organ allografts
Prior radiotherapy, or prior intratumor injection therapy, to areas of measurable disease that are used as target indicator lesions, unless progression has occurred at that site or measurable disease has developed outside the treatment area
Pregnancy or lactation
History of second cancer
Known hypersensitivity to temozolomide or imatinib
Use of any experimental therapy within 3 weeks prior to baseline evaluations done prior to enrollment

Study is for people with:

Melanoma

Phase:

Phase 1

Estimated Enrollment:

32

Study ID:

NCT00667953

Recruitment Status:

Terminated

Sponsor:

Abramson Cancer Center at Penn Medicine

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There is 1 Location for this study

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Abramson Cancer Center at University of Pennsylvania
Philadelphia Pennsylvania, 19104, United States

How clear is this clinincal trial information?

Study is for people with:

Melanoma

Phase:

Phase 1

Estimated Enrollment:

32

Study ID:

NCT00667953

Recruitment Status:

Terminated

Sponsor:


Abramson Cancer Center at Penn Medicine

How clear is this clinincal trial information?

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