A Multi-center Study of VAL-083 in Patients With Recurrent Platinum Resistant Ovarian Cancer

PHASE1/PHASE2WithdrawnINTERVENTIONAL
0
Timeline

Start Date

March 31, 2021

Primary Completion Date

March 31, 2022

Study Completion Date

September 30, 2022

Conditions
Ovarian Cancer
Interventions
DRUG

VAL-083, Dianhydrogalactitol

VAL-083 given by intravenous infusion with a starting dose of 60 mg/m2 once weekly. If this regimen is well tolerated for at least three sequential weekly treatments the patient's dose may be escalated to 67 mg/m2 i.v. If the 67 mg/m2 dose is well tolerated for at least three sequential weekly treatments the patient's dose may be escalated to 75 mg/m2 i.v. once weekly for the remainder of the study. Dosing will be conducted once per week for a total of 16 weeks.

Trial Locations (3)

37203

Sarah Cannon Research Institute, Nashville

48202

Henry Ford Hospital, Detroit

85013

St. Joseph's Hospital and Medical Center, Phoenix

Sponsors
All Listed Sponsors
lead

DelMar Pharmaceuticals, Inc.

INDUSTRY