NUC-1031 in Patients With Platinum-Resistant Ovarian Cancer

PHASE2TerminatedINTERVENTIONAL
Enrollment

53

Participants

Timeline

Start Date

September 28, 2017

Primary Completion Date

December 31, 2019

Study Completion Date

December 31, 2019

Conditions
Ovarian Cancer
Interventions
DRUG

NUC-1031 500 mg

NUC-1031 500 mg/m2 on Days 1, 8, and 15 of a 28-day cycle.

DRUG

NUC-1031 750mg

NUC-1031 750 mg/m2 on Days 1, 8, and 15 of a 28-day cycle

Trial Locations (17)

33705

Florida Cancer Specialists and Research Institute, St. Petersburg

37203

Nashville Tennessee Oncology, Nashville

64132

SCRI - HCA Health Midwest, Kansas City

75702

Texas Oncology - Tyler, Tyler

77380

Texas Oncology The Woodlands, Gynecologic Oncology, The Woodlands

78745

Texas Oncology - South Austin, Austin

80228

Rocky Mountain Cancer Centers, LLP, Lakewood

85016

Arizona Oncology Associates, PC - HAL, Phoenix

85711

Arizona Oncology Associates, PC - HOPE, Tucson

55435-2150

Minnesota Oncology Hematology, P.A., Edina

EH4 2XR

Edinburgh Cancer Centre, Edinburgh

G12 0YN

Cancer Research UK Clinical Trial Unit, Glasgow

EC1A 7BE

St Bartholomew's Hospital, London

NW1 2PG

University College London Hospital, London

SW3 6JJ

Royal Marsden Hospital, London

W12 0HS

Imperial College Healthcare NHS Trust, London

OX3 7LE

Oxford University Hospital Foundation Trust, Oxford

Sponsors

Lead Sponsor

All Listed Sponsors
lead

NuCana plc

OTHER

NCT03146663 - NUC-1031 in Patients With Platinum-Resistant Ovarian Cancer | Biotech Hunter | Biotech Hunter