Evaluation of KX2-391 in Patients With Advanced Malignancies

PHASE1CompletedINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

November 30, 2007

Primary Completion Date

March 31, 2010

Study Completion Date

May 31, 2011

Conditions
Solid TumorsLymphoma
Interventions
DRUG

KX2-391

2 mg (starting dose)rising dose, oral dosing, twice daily, 21 day cycle(s); until progression or unacceptable toxicity develops

Trial Locations (2)

19111

Fox Chase Cancer Center, Philadelphia

77030

MD Anderson Cancer Center, Houston

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Athenex, Inc.

INDUSTRY

NCT00658970 - Evaluation of KX2-391 in Patients With Advanced Malignancies | Biotech Hunter | Biotech Hunter