GOG-0281
Terminated
Protocol Information
A Randomized Phase II/III Study to Assess the Efficacy of Trametinib (GSK 1120212) in Patients with Recurrent or Progressive Low-Grade Serous Ovarian Cancer or Peritoneal Cancer
Principal Investigator
David Gershenson
Status
Terminated
Open to Accrual
February 27, 2014
Temporarily Closed to Accrual
February 2, 2016
Open to Accrual
February 5, 2016
Closed to Accrual
April 10, 2018
Closed to Accrual & Treatment
July 14, 2025
Complete
July 14, 2025
Terminated
October 27, 2025
Disease Site
Gynecologic [GY] Ovarian
Phase
II/III
Developmental Therapeutics
No
Primary Objective
To estimate the progression-free survival (PFS) hazard ratio of trametinib compared to that of “commercially available therapies” consisting of one of five commercially available agents in women with recurrent low-grade serous carcinoma of the ovary or peritoneum previously treated with platinum-based chemotherapy.
Patient Population
Progression-free survival (PFS) hazard ratio of trametinib compared to that of “commercially available therapies” consisting of one of five commercially available agents in women with recurrent low-grade serous carcinoma of the ovary or peritoneum previously treated with platinum-based chemotherapy.
Target Accrual
250
Protocol Documents
Available via the National Cancer Institute (NCI) Cancer Trials Support Unit (CTSU) website.