search
Back to results

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

Primary Purpose

Endometrial Carcinoma

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
GDC-0980
Sponsored by
Genentech, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Endometrial Carcinoma

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients must have recurrent or persistent endometrial carcinoma that is refractory to curative therapy or established treatments
  • Histologic confirmation of the original primary tumor is required
  • Histologic or cytologic confirmation of the recurrent/progressive disease is desired
  • Patients must have had at least one but no more than two prior chemotherapeutic regimens for management of endometrial carcinoma
  • Disease that is measurable per RECIST v1.1
  • No active infection requiring antibiotics
  • Any hormonal therapy directed at the malignant tumor must be discontinued at least 2 weeks prior to first study treatment
  • Any other prior therapy directed at the malignant tumor, including immunologic agents and radiotherapy, must be discontinued at least 2 weeks prior to first study treatment
  • Adequate hematologic and end organ function

Exclusion Criteria:

  • Type I diabetes or Type II diabetes requiring insulin
  • Prior use of mTOR/PI3K inhibitor
  • Current dyspnea at rest or any requirement for supplemental oxygen therapy to perform activities of daily living
  • Previous diagnosis of pulmonary fibrosis of any cause
  • History of myocardial infarction or unstable angina within 6 months prior to first study treatment
  • Congestive heart failure
  • History of malabsorption syndrome or other condition that would interfere with enteral absorption
  • Clinically significant history of liver disease, including cirrhosis and current alcohol abuse
  • Presence of positive test results for hepatitis B or hepatitis C
  • Known HIV infection
  • Active autoimmune disease that is not controlled by nonsteroidal anti inflammatory drugs
  • Need for current chronic corticosteroid therapy
  • Pregnancy, lactation, or breastfeeding
  • Current severe, uncontrolled systemic disease
  • Major surgical procedure or significant traumatic injury within 28 days prior to Day 1 or anticipation of the need for major surgery during the course of study treatment
  • Uncontrolled hypercalcemia
  • Leptomeningeal disease as a manifestation of cancer
  • Known untreated or active brain metastases
  • Grade >=2 hypercholesterolemia or hypertriglyceridemia

Sites / Locations

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

A

Arm Description

Outcomes

Primary Outcome Measures

Objective tumor response as assessed by the investigator using RECIST v1.1
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

Secondary Outcome Measures

Overall survival (OS), defined as the time from treatment initiation until death from any cause
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
Incidence of adverse events
Nature of adverse events
Severity of adverse events

Full Information

First Posted
October 18, 2011
Last Updated
August 9, 2016
Sponsor
Genentech, Inc.
search

1. Study Identification

Unique Protocol Identification Number
NCT01455493
Brief Title
A Study of GDC-0980 in the Treatment of Recurrent or Persistent Endometrial Carcinoma
Official Title
A Multicenter, Single-Arm, Open-Label, Phase II Study of GDC-0980 for The Treatment of Recurrent or Persistent Endometrial Carcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
August 2016
Overall Recruitment Status
Completed
Study Start Date
December 2011 (undefined)
Primary Completion Date
March 2013 (Actual)
Study Completion Date
January 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Genentech, Inc.

4. Oversight

5. Study Description

Brief Summary
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. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Endometrial Carcinoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
56 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
GDC-0980
Intervention Description
Oral daily dose
Primary Outcome Measure Information:
Title
Objective tumor response as assessed by the investigator using RECIST v1.1
Time Frame
up to approximately 23 months
Title
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
Secondary Outcome Measure Information:
Title
Overall survival (OS), defined as the time from treatment initiation until death from any cause
Time Frame
up to approximately 36 months
Title
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
Title
Incidence of adverse events
Time Frame
up to approximately 23 months
Title
Nature of adverse events
Time Frame
up to approximately 23 months
Title
Severity of adverse events
Time Frame
up to approximately 23 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients must have recurrent or persistent endometrial carcinoma that is refractory to curative therapy or established treatments Histologic confirmation of the original primary tumor is required Histologic or cytologic confirmation of the recurrent/progressive disease is desired Patients must have had at least one but no more than two prior chemotherapeutic regimens for management of endometrial carcinoma Disease that is measurable per RECIST v1.1 No active infection requiring antibiotics Any hormonal therapy directed at the malignant tumor must be discontinued at least 2 weeks prior to first study treatment Any other prior therapy directed at the malignant tumor, including immunologic agents and radiotherapy, must be discontinued at least 2 weeks prior to first study treatment Adequate hematologic and end organ function Exclusion Criteria: Type I diabetes or Type II diabetes requiring insulin Prior use of mTOR/PI3K inhibitor Current dyspnea at rest or any requirement for supplemental oxygen therapy to perform activities of daily living Previous diagnosis of pulmonary fibrosis of any cause History of myocardial infarction or unstable angina within 6 months prior to first study treatment Congestive heart failure History of malabsorption syndrome or other condition that would interfere with enteral absorption Clinically significant history of liver disease, including cirrhosis and current alcohol abuse Presence of positive test results for hepatitis B or hepatitis C Known HIV infection Active autoimmune disease that is not controlled by nonsteroidal anti inflammatory drugs Need for current chronic corticosteroid therapy Pregnancy, lactation, or breastfeeding Current severe, uncontrolled systemic disease Major surgical procedure or significant traumatic injury within 28 days prior to Day 1 or anticipation of the need for major surgery during the course of study treatment Uncontrolled hypercalcemia Leptomeningeal disease as a manifestation of cancer Known untreated or active brain metastases Grade >=2 hypercholesterolemia or hypertriglyceridemia
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Clinical Trials
Organizational Affiliation
Genentech, Inc.
Official's Role
Study Director
Facility Information:
City
Phoenix
State/Province
Arizona
ZIP/Postal Code
85013
Country
United States
City
Newport Beach
State/Province
California
ZIP/Postal Code
92663
Country
United States
City
Orange
State/Province
California
ZIP/Postal Code
92868
Country
United States
City
Palo Alto
State/Province
California
ZIP/Postal Code
94305
Country
United States
City
San Francisco
State/Province
California
ZIP/Postal Code
94115
Country
United States
City
Denver
State/Province
Colorado
ZIP/Postal Code
80220
Country
United States
City
New Haven
State/Province
Connecticut
ZIP/Postal Code
06511
Country
United States
City
Boca Raton
State/Province
Florida
ZIP/Postal Code
33487
Country
United States
City
Orlando
State/Province
Florida
ZIP/Postal Code
32804
Country
United States
City
West Palm Beach
State/Province
Florida
ZIP/Postal Code
33401
Country
United States
City
Hinsdale
State/Province
Illinois
ZIP/Postal Code
60521
Country
United States
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46237
Country
United States
City
Louisville
State/Province
Kentucky
ZIP/Postal Code
40202
Country
United States
City
Scarborough
State/Province
Maine
ZIP/Postal Code
04074
Country
United States
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21231
Country
United States
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115-6084
Country
United States
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02215
Country
United States
City
Voorhees
State/Province
New Jersey
ZIP/Postal Code
08043
Country
United States
City
New York
State/Province
New York
ZIP/Postal Code
10016
Country
United States
City
New York
State/Province
New York
ZIP/Postal Code
10017
Country
United States
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27710
Country
United States
City
Winston-salem
State/Province
North Carolina
ZIP/Postal Code
27103
Country
United States
City
Oklahoma City
State/Province
Oklahoma
ZIP/Postal Code
73104
Country
United States
City
Abington
State/Province
Pennsylvania
ZIP/Postal Code
19001
Country
United States
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States
City
Salt Lake City
State/Province
Utah
ZIP/Postal Code
84112
Country
United States
City
Seattle
State/Province
Washington
ZIP/Postal Code
98195
Country
United States
City
Milwaukee
State/Province
Wisconsin
ZIP/Postal Code
53226
Country
United States

12. IPD Sharing Statement

Learn more about this trial

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

We'll reach out to this number within 24 hrs