Melanoma Clinical Trial

A Study to Evaluate RAF265, an Oral Drug Administered to Subjects With Locally Advanced or Metastatic Melanoma

Summary

The purpose of this study is to determine the safety profile, pharmacokinetics, pharmacodynamics and maximum tolerated dose of RAF265 in patients with locally advanced and metastatic melanoma.

Phase II portion of study (dose expansion) has been cancelled with Amendment 7 as of Dec 2011.

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Full Description

The Ras/Raf/MEK/ERK pathway plays a prominent role in controlling several key cellular functions including growth, proliferation and survival. B-Raf is a member of the Ras/Raf/MEK/ERK pathway and is frequently mutated in melanoma resulting in activation of the MAPK pathway. RAF265 is a novel, orally active, small molecule with potent inhibitory activity against B-Raf kinase and additional antiangiogenic activity through inhibition of vascular endothelial growth factor receptor type 2 (VEGFR-2) in non-clinical studies.

The primary objectives of this study are to determine the maximum tolerated dose (MTD), dose limiting toxicities (DLTs), and the safety profile of RAF265 when administered orally to subjects with locally advanced or metastatic melanoma; to determine the plasma pharmacokinetics (PKs) of orally administered RAF265; and to evaluate potential pharmacodynamic effects of RAF265 using tumor biopsies, peripheral blood samples, and tumor imaging.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Confirmed diagnosis of melanoma, locally advanced AJCC Stage IIIB to metastatic Stage IV
Measurable disease - at least one lesion measured in at least one dimension as ≥ 20 mm with conventional techniques or ≥ 10 mm with spiral computed tomography (CT) scan
ECOG performance status of 0 or 1
No concurrent anticancer or investigational therapy for at least 4 weeks prior to enrollment
No major surgery for at least 4 weeks prior to enrollment

Exclusion Criteria:

Significant cardiac disease or other significant medical/psychiatric disease
History of primary central nervous system tumor or brain metastases
History of melena, hematemesis, or hemoptysis within the last 3 months
Previous therapy with certain molecularly targeted agents

Study is for people with:

Melanoma

Phase:

Phase 1

Estimated Enrollment:

104

Study ID:

NCT00304525

Recruitment Status:

Completed

Sponsor:

Novartis Pharmaceuticals

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There are 11 Locations for this study

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University of Colorado Univ.ofColoradoCancerCenter
Aurora Colorado, 80045, United States
Georgia Regents University Cancer Clinical Research Unit
Augusta Georgia, 30912, United States
Sidney Kimmel Comprehensive Cancer Center/Johns Hopkins Med. Medical Oncology
Baltimore Maryland, 21231, United States
Massachusetts General Hospital Dept of Cancer for Melanoma
Boston Massachusetts, 02114, United States
Dana Farber Cancer Institute DFCI
Boston Massachusetts, 02115, United States
Beth Israel Deaconess Medical Center Dept.ofBethIsraelDeaconess(3)
Boston Massachusetts, 02215, United States
University of Pennsylvania Health System Dept of Hospital of UnivofPenn
Philadelphia Pennsylvania, 19104, United States
University of Pittsburgh Cancer Institute Dept of Hillman Cancer Center
Pittsburgh Pennsylvania, 15232, United States
Vanderbilt University Medical Center Dept. of Cancer Center
Nashville Tennessee, 37232, United States
University of Texas/MD Anderson Cancer Center Onc. Dept,
Houston Texas, 77030, United States
Novartis Investigative Site
Zürich , 8091, Switzerland

How clear is this clinincal trial information?

Study is for people with:

Melanoma

Phase:

Phase 1

Estimated Enrollment:

104

Study ID:

NCT00304525

Recruitment Status:

Completed

Sponsor:


Novartis Pharmaceuticals

How clear is this clinincal trial information?

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