Melanoma Clinical Trial

Safety and Efficacy of an Immune Response Modifier to Treat Inoperable Advanced Melanoma Skin Lesions

Summary

Study 1501-852A is a Phase 1 Study with the objective of determining safety and the highest tolerated dose of an immune response modifier cream directly applied to advanced, inoperable, melanoma skin lesions. The study will also measure blood levels of the drug and examine the potential anti-tumor activity of the cream.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Have melanoma cutaneous metastasis or lentigo maligna melanoma unresectable and for which standard curative or palliative measures do not exist or are no longer effective.
Eastern Cooperative Oncology Group (ECOG) performance status less than or equal to 2
Have a life expectancy of 4 months
Have normal organ and bone marrow function

Exclusion Criteria:

Need for non-steroidal anti-inflammatory drugs (NSAIDs) during the study
Have a body mass index (BMI)> 30 kg/m2
Have a history of, or clinical evidence of, myocardial ischemia, congestive heart failure, or myocardial arrhythmias requiring treatment within the past 6 months
Have uncontrolled intercurrent or chronic illness, but not limited to, ongoing or active infection such as hepatitis B or C, immune dysfunction such as autoimmune disease, endocrine dysfunction such as hypo- or hyperthyroidism, psychiatric illness such as depression or suicidal tendency or social situations that would limit compliance with study requirements
Have a history of disease requiring ongoing steroid treatment
Have a history of seizure disorder (other than febrile seizures in childhood)
Have a history of clinically significant coagulation or bleeding disorders or abnormalities
Are HIV positive. HIV positive subjects are excluded from the study because of possible interactions with the immunomodulatory effects of 852A and because of potential pharmacokinetic interactions associated with combination retroviral therapy.

Study is for people with:

Melanoma

Phase:

Phase 1

Study ID:

NCT00091689

Recruitment Status:

Completed

Sponsor:

Pfizer

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There is 1 Location for this study

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Dartmouth-Hitchcock Medical Center
Lebanon New Hampshire, , United States
Oklahoma Medical Research Foundation
Oklahoma City Oklahoma, , United States

How clear is this clinincal trial information?

Study is for people with:

Melanoma

Phase:

Phase 1

Study ID:

NCT00091689

Recruitment Status:

Completed

Sponsor:


Pfizer

How clear is this clinincal trial information?

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