A Phase 2 interventional study of GDC-0980 in Endometrial Carcinoma, sponsored by Genentech, Inc.. Completed at 28 sites in United States. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2016-08-11.
Sponsored by Genentech, Inc. · Phase 2, Interventional, and Treatment
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.
6,741 studies on the registry are indexed under Carcinoma; 1,161 are open to participants now.
This study's enrollment of 56 is above the median of 45 across 5,170 interventional studies indexed under Carcinoma.
Browse Carcinoma studies →Genentech, Inc. is the lead sponsor of 507 studies on the registry; 23 are open to participants now.
Of its 90 completed or terminated interventional studies of FDA-regulated products, 50 (56%) have results posted.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Drug: GDC-0980
Oral daily dose
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 study is completed, as verified in Aug 2016. You cannot join it, but the record below documents what was studied.
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Genentech, Inc.