Phase 1 Study of MPC-6827 and Temozolomide in Metastatic Melanoma

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

22

Participants

Timeline

Start Date

March 31, 2008

Primary Completion Date

August 31, 2009

Study Completion Date

August 31, 2009

Conditions
Metastatic Melanoma
Interventions
DRUG

MPC-6827 + Temozolomide

MPC-6827 at 2.1mg/m2, 2.7mg/m2 or 3.3mg/m2 administered by intravenous infusion over 2 hours once weekly for three weeks in a 4 week cycle. Temozolomide at 85 mg/m2 administered orally daily for 21 days in a 4 week cycle.

Trial Locations (5)

29605

Cancer Centers of the Carolinas, Greenville

34761

Cancer Centers of Florida, Ocoee

77030

University of Texas MD Anderson Cancer Center, Houston

84112

Huntsman Cancer Institute at the University of Utah, Salt Lake City

90025

The Angeles Clinic, Los Angeles

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Myrexis Inc.

INDUSTRY

NCT00609011 - Phase 1 Study of MPC-6827 and Temozolomide in Metastatic Melanoma | Biotech Hunter | Biotech Hunter