Melanoma Clinical Trial

A Safety and MORAb-028 Dose Determination Study in Subjects With Metastatic Melanoma

Summary

The purpose of this study is to evaluate whether therapy with MORAb-028 is safe, effective, and to determine the appropriate dose of MORAb-028 in the treatment of metastatic melanoma.

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Full Description

Melanoma is a serious form of skin cancer. If untreated, the melanoma can spread beyond the original affected tissue and invade distant tissue and organs. Treatment for metastatic melanoma includes medical treatments (chemotherapy or immunotherapy), surgery, or radiation therapy. MORAb-028 is a recombinant human immunoglobulin M (IgM) monoclonal antibody that recognizes a cell surface diacyl ganglioside named disialoganglioside (GD2). GD2 is overexpressed in tumors of neuro-ectodermal origin such as melanomas, neuroblastomas, small-cell lung carcinomas, and many sarcomas, while absent in most normal tissues. GD2 expression has been demonstrated in human melanoma and small cell lung cancer by thin layer chromatography and radiolabeled anti-GD2 antibody detection. It is hypothesized that one mode of action of MORAb-028 is complement-dependent cytotoxicity. Complement-dependent cytotoxicity is a mechanism for killing tumor cells in which an antibody bound to the target cell surface fixes complement, which results in assembly of the complement membrane attack complex that punches holes in the target cell membrane resulting in subsequent cell lysis. IgMs strongly bind to C1Q and robustly activate complement-dependent cytotoxicity. MORAb-028 is being developed as a potential therapy for GD2-positive tumors.

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Eligibility Criteria

Inclusion Criteria:

Measurable metastatic melanoma that has failed standard therapy
Males and females greater than or equal to 18 years of age
Life expectancy of greater than or equal to 3 months

Exclusion Criteria:

Significant cardiovascular impairment
Clinically significant illness, medical condition, surgical history, or laboratory abnormality that could affect the safety of the subject or negatively impact the study results
Chemotherapy, radiotherapy, or immunotherapy within 3 weeks prior to administration to MORAb-028

Study is for people with:

Melanoma

Phase:

Phase 1

Estimated Enrollment:

18

Study ID:

NCT01212276

Recruitment Status:

Terminated

Sponsor:

Morphotek

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There is 1 Location for this study

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Memorial Sloan-Kettering Cancer Center
New York New York, 10022, United States

How clear is this clinincal trial information?

Study is for people with:

Melanoma

Phase:

Phase 1

Estimated Enrollment:

18

Study ID:

NCT01212276

Recruitment Status:

Terminated

Sponsor:


Morphotek

How clear is this clinincal trial information?

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