Melanoma Clinical Trial

Study to Determine the Effectiveness of GSK1120212 in BRAF Mutation-positive Melanoma Previously Treated With or Without a BRAF Inhibitor

Summary

MEK113583 is a Phase II open-label, multi-site study to investigate the objective response rate, safety, and pharmacokinetics of GSK1120212 in subjects with BRAF mutation-positive melanoma who were previously treated with or without a BRAF inhibitor. GSK1120212 is a potent and highly selective inhibitor of MEK activation and kinase activity.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Metastatic cutaneous melanoma that was previously treated with: (Cohort A) a BRAF inhibitor either with or without other prior therapy. (Cohort B) at least 1 prior chemotherapy or immunotherapy, without treatment with a BRAF inhibitor.
Documented positive BRAF mutation (V600E, V600K, or V600D).
Subjects must provide archived tumor tissue or undergo fresh tumor biopsy prior to enrollment.
The subject must have a radiographically measurable tumor.
The subject is able to carry out daily life activities without significant difficulty (ECOG performance status score of 0 or 1).
Able to swallow and retain oral medication.
Sexually active subjects must use acceptable methods of contraception during the course of the study.
Adequate organ system function and blood cell counts.

Exclusion Criteria:

The subject has had major surgery or received certain types of cancer therapy within 21 days before starting the study.
Previous treatment with a MEK inhibitor.
Current use of a prohibited medication listed in the protocol.
Uncontrolled glaucoma.
Brain metastasis, unless previously treated with surgery or stereotactic radiosurgery, and the disease has been stable for at least 2 months prior to enrollment.
Current severe or uncontrolled systemic disease.
History of clinically significant heart, lung, or eye/vision problems.
Significant unresolved side effects from previous anti-cancer therapy.
The subject is pregnant or breastfeeding.

Study is for people with:

Melanoma

Phase:

Phase 2

Estimated Enrollment:

97

Study ID:

NCT01037127

Recruitment Status:

Completed

Sponsor:

GlaxoSmithKline

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There are 10 Locations for this study

See Locations Near You

GSK Investigational Site
Los Angeles California, 90024, United States
GSK Investigational Site
Aurora Colorado, 80045, United States
GSK Investigational Site
New York New York, 10016, United States
GSK Investigational Site
Philadelphia Pennsylvania, 19104, United States
GSK Investigational Site
Nashville Tennessee, 37203, United States
GSK Investigational Site
Nashville Tennessee, 37232, United States
GSK Investigational Site
Houston Texas, 77030, United States
GSK Investigational Site
Westmead New South Wales, 2145, Australia
GSK Investigational Site
East Melbourne Victoria, 3002, Australia
GSK Investigational Site
Nedlands Western Australia, 6009, Australia

How clear is this clinincal trial information?

Study is for people with:

Melanoma

Phase:

Phase 2

Estimated Enrollment:

97

Study ID:

NCT01037127

Recruitment Status:

Completed

Sponsor:


GlaxoSmithKline

How clear is this clinincal trial information?

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