Clinical and Molecular-Metabolic Phase II Trial of Perifosine for Recurrent/Progressive Malignant Gliomas

PHASE2CompletedINTERVENTIONAL
Enrollment

32

Participants

Timeline

Start Date

May 31, 2006

Primary Completion Date

November 11, 2019

Study Completion Date

November 11, 2019

Conditions
Malignant GliomasCNSBrain CancerCancer
Interventions
DRUG

Perifosine

"Dosing will be continuous, and for the purpose of this trial a cycle will be defined as 28 days. Perifosine will be given as a 600 mg loading dose on day 1. The loading dose will be divided into 4 equal doses of 150 mg each. The first 3 doses should be given with food in the adult day hospital to allow intravenous antiemetic prophylaxis, and 4th dose at bedtime at home. The interval between doses of perifosine should be no less than 4 hours. On day 2, patients will start the maintenance dose of 100 mg daily at bedtime at home.~In addition to baseline serum, all patients will have weekly serum drawn during weeks 2-4."

Trial Locations (1)

10065

Memorial Sloan-Kettering Cancer Center, New York

All Listed Sponsors
collaborator

Keryx Biopharmaceuticals

INDUSTRY

collaborator

Keryx / AOI Pharmaceuticals, Inc.

INDUSTRY

collaborator

Online Collaborative Oncology Group

OTHER

collaborator

University of Wisconsin, Madison

OTHER

collaborator

Columbia University

OTHER

lead

Memorial Sloan Kettering Cancer Center

OTHER

NCT00590954 - Clinical and Molecular-Metabolic Phase II Trial of Perifosine for Recurrent/Progressive Malignant Gliomas | Biotech Hunter | Biotech Hunter