Efficacy Study of Maintenance IT-101 Therapy for Ovarian Cancer Patients.

PHASE2WithdrawnINTERVENTIONAL
0
Timeline

Start Date

September 30, 2008

Primary Completion Date

October 31, 2009

Study Completion Date

May 31, 2010

Conditions
CancerOvarian CancerSolid Tumor
Interventions
DRUG

IT-101 (12mg/m2/dose)

Patients who satisfy the inclusion/exclusion criteria will receive a blinded infusion of IT-101 (12mg/m2/dose) every other week until disease progression.

DRUG

IT-101 (15mg/m2/dose)

Patients who satisfy the inclusion/exclusion criteria will receive an infusion of IT-101 (15mg/m2) every other week until disease progression.

DRUG

5% Dextrose (Placebo)

Patients who satisfy the inclusion/exclusion criteria will receive an infusion of placebo every other week until disease progression.

Trial Locations (7)

11718

Schwartz Gynecologic Onclology, PLLC, Brightwaters

23601

Riverside Gynecology & Oncology, Newport News

44718

Gabrail Cancer Center, Canton

55455

University of Minnesota Medical Center, Minneapolis

62526

Decatur Memorial Hospital, Clinical Research Department/ Cancer Care Specialists of Illinois, Decatur

77030

The Methodist Hospital, Houston

97403

Chattanooga GYN Oncology, Chattanooga

Sponsors
All Listed Sponsors
lead

NewLink Genetics Corporation

INDUSTRY

NCT00753740 - Efficacy Study of Maintenance IT-101 Therapy for Ovarian Cancer Patients. | Biotech Hunter | Biotech Hunter