This is a multicenter, single-arm, open-label Phase II study to evaluate the activity of GDC-0980 in patients with recurrent or persistent endometrial cancer. The safety, tolerability, and pharmacokinetics of GDC-0980 will also be evaluated.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
56
Oral daily dose
Unnamed facility
Phoenix, Arizona, United States
Objective tumor response as assessed by the investigator using RECIST v1.1
Time frame: up to approximately 23 months
Progression-free survival (PFS), defined as the time from the first GDC-0980 treatment to disease progression as assessed by the investigator using RECIST v1.1, or death from any cause while on study
Time frame: at 6 months
Overall survival (OS), defined as the time from treatment initiation until death from any cause
Time frame: up to approximately 36 months
Duration of objective tumor response defined as the time from first observation of an objective tumor response until first observation of disease progression as assessed by the investigator using RECIST v1.1
Time frame: up to approximately 23 months
Incidence of adverse events
Time frame: up to approximately 23 months
Nature of adverse events
Time frame: up to approximately 23 months
Severity of adverse events
Time frame: up to approximately 23 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Unnamed facility
Newport Beach, California, United States
Unnamed facility
Orange, California, United States
Unnamed facility
Palo Alto, California, United States
Unnamed facility
San Francisco, California, United States
Unnamed facility
Denver, Colorado, United States
Unnamed facility
New Haven, Connecticut, United States
Unnamed facility
Boca Raton, Florida, United States
Unnamed facility
Orlando, Florida, United States
Unnamed facility
West Palm Beach, Florida, United States
...and 18 more locations