Study of the Safety and Tolerability of Oral Capsule Form of PCI-24781 in Advanced Cancer Patients

PHASE1CompletedINTERVENTIONAL
Enrollment

36

Participants

Timeline

Start Date

November 30, 2007

Primary Completion Date

June 30, 2010

Study Completion Date

September 30, 2010

Conditions
Neoplasms by SiteLymphoma, Non-hodgkinHodgkin DiseaseMultiple MyelomaLeukemia, Lymphocytic, Chronic
Interventions
DRUG

PCI-24781

"Up to 7 cohorts will receive PCI-24781 orally at doses starting at 30 mg/m2 three times a day approximately 4 hours apart (TID), up to 90 mg/m2, administered 5 days/week during the first 21 days of each 28 day cycle until MTD is reached. If a dose limiting toxicity (DLT) occurs, then the next cohort will receive PCI-24781 twice a day approximately 4 hours apart (BID). If a DLT occurs on the BID schedule, the subsequent cohort will receive PCI-24781 BID for 7 days every other week (2 times in a 28 day cycle). If a DLT occurs on this dosing schedule, then the next cohort will receive PCI-24781 BID for 5 days/week every other week (2 times in a 28 day cycle) until the maximum tolerated dose is reached."

Trial Locations (4)

37203

Sarah Cannon Research Institue, Nashville

60637

University of Chicago, Chicago

77030

MD Anderson Cancer Center, Houston

94904

California Cancer Care, Greenbrae

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pharmacyclics LLC.

INDUSTRY

NCT00562224 - Study of the Safety and Tolerability of Oral Capsule Form of PCI-24781 in Advanced Cancer Patients | Biotech Hunter | Biotech Hunter