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Completed Phase 2 Interventional

A Study of GDC-0980 in the Treatment of Recurrent or Persistent Endometrial Carcinoma

ClinicalTrials.gov ID: NCT01455493

Public ClinicalTrials.gov record NCT01455493. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 2, 2026, 11:19 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Single-Arm, Open-Label, Phase II Study of GDC-0980 for The Treatment of Recurrent or Persistent Endometrial Carcinoma

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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 identification

NCT ID
NCT01455493
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Genentech, Inc.
Industry
Enrollment
56 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 2011 (Type not available)
Primary completion
Mar 2013 (Actual)
Completion
Jan 2014 (Actual)
Last update posted
Aug 11, 2016

2011 – 2014

United States locations

U.S. sites
28
U.S. states
19
U.S. cities
26
Facility City State ZIP Site status
Not listed Phoenix Arizona 85013 —
Not listed Newport Beach California 92663 —
Not listed Orange California 92868 —
Not listed Palo Alto California 94305 —
Not listed San Francisco California 94115 —
Not listed Denver Colorado 80220 —
Not listed New Haven Connecticut 06511 —
Not listed Boca Raton Florida 33487 —
Not listed Orlando Florida 32804 —
Not listed West Palm Beach Florida 33401 —
Not listed Hinsdale Illinois 60521 —
Not listed Indianapolis Indiana 46237 —
Not listed Louisville Kentucky 40202 —
Not listed Scarborough Maine 04074 —
Not listed Baltimore Maryland 21231 —
Not listed Boston Massachusetts 02115-6084 —
Not listed Boston Massachusetts 02215 —
Not listed Voorhees Township New Jersey 08043 —
Not listed New York New York 10016 —
Not listed New York New York 10017 —
Not listed Durham North Carolina 27710 —
Not listed Winston-Salem North Carolina 27103 —
Not listed Oklahoma City Oklahoma 73104 —
Not listed Abington Pennsylvania 19001 —
Not listed Pittsburgh Pennsylvania 15213 —
Not listed Salt Lake City Utah 84112 —
Not listed Seattle Washington 98195 —
Not listed Milwaukee Wisconsin 53226 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01455493, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 11, 2016 · Synced Oct 2, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01455493 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →