MSX-122 Administered Orally in Patients With Refractory Metastatic or Locally Advanced Solid Tumors

PHASE1SuspendedINTERVENTIONAL
Enrollment

27

Participants

Timeline

Start Date

November 30, 2007

Primary Completion Date

December 31, 2008

Study Completion Date

March 31, 2009

Conditions
Solid Tumors
Interventions
DRUG

MSX-122

"Dosage form = capsule~Starting Dose (First Patient Cohort - Dose Level 1) = 50 mg taken orally once daily, 7 days per week for 4 weeks (total of 28 days), followed immediately by a second course of 28 days with identical dosage form and schedule. (Each patient in each cohort treated for a minimum of 56 days, unless obviated by toxicity.)~* If there is no evidence of toxicity at the current dose level, then the dose of MSX-122 will be increased by 100% for the next patient cohort.~* If a grade 1-2 toxicity is observed, then the dose will be increased by 50% for the next patient cohort.~* If a grade 3 toxicity (non-dose limiting toxicity) is observed then the dose will be increased by 25% for the next patient cohort."

Trial Locations (1)

77030

U.T.M.D. Anderson Cancer Center, Houston

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Metastatix, Inc.

INDUSTRY