A Phase II, International Open Label Trial of Minnelide™ in Patients With Refractory Pancreatic Cancer

PHASE2CompletedINTERVENTIONAL
Enrollment

19

Participants

Timeline

Start Date

April 10, 2017

Primary Completion Date

July 1, 2019

Study Completion Date

July 1, 2019

Conditions
Pancreatic Cancer
Interventions
DRUG

Minnelide

Minnelide will be administered at the dose of 0.67 mg/m2 as a 30 min infusion intravenously daily on days 1-21 of each cycle followed by a 7 day rest period (days 22-28).

Trial Locations (3)

19104

University of Pennsylvania, Philadelphia

85258

HonorHealth Research Institute, Scottsdale

92037

Moores UC San Diego Cancer Center, La Jolla

Sponsors
All Listed Sponsors
collaborator

Barts & The London NHS Trust

OTHER

collaborator

Translational Genomics Research Institute

OTHER

collaborator

Stand Up To Cancer

OTHER

collaborator

Cancer Research UK

OTHER

collaborator

Lustgarten Foundation

OTHER

collaborator

Queen Mary University of London

OTHER

lead

Minneamrita Therapeutics LLC

INDUSTRY

NCT03117920 - A Phase II, International Open Label Trial of Minnelide™ in Patients With Refractory Pancreatic Cancer | Biotech Hunter | Biotech Hunter