Prospective Translational Study Investigating Molecular Predictors of Resistance and Response to Regorafenib Monotherapy

CompletedOBSERVATIONAL
Enrollment

49

Participants

Timeline

Start Date

January 31, 2015

Primary Completion Date

January 31, 2017

Study Completion Date

July 31, 2017

Conditions
Metastatic Colorectal Cancer
Interventions
DRUG

Regorafenib

"Patients meeting all of the inclusion criteria and none of the exclusion criteria will receive regorafenib 160 mg orally (po) od for 3 weeks of every 4-week cycle. Each cycle will comprise 3 weeks of treatment followed by 1 week without treatment, hereafter described as 3 weeks on/1 week off. Each 160-mg dose will include four regorafenib 40-mg tablets."

Trial Locations (1)

SM2 5PT

The Royal Marsden NHS Foundation Trust London and Surrey, Carshalton

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Bayer

INDUSTRY

lead

Royal Marsden NHS Foundation Trust

OTHER