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



Status:Completed
Conditions:Cervical Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:8/3/2016
Start Date:December 2011
End Date:January 2014

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

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.


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
We found this trial at
26
sites
Newport Beach, California 92660
1158
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from
Newport Beach, CA
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1227
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Abington, PA
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1148
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Baltimore, MD
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1299
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Boca Raton, FL
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Boston, MA
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409
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Denver, CO
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1051
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Durham, NC
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594
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Hinsdale, IL
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643
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Indianapolis, IN
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657
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Louisville, KY
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630
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Milwaukee, WI
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1344
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New Haven, CT
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1290
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New York, NY
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158
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Oklahoma City, OK
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1154
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Orange, CA
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1139
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Orlando, FL
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1328
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Palo Alto, CA
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853
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Phoenix, AZ
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971
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Pittsburgh, PA
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779
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Salt Lake City, UT
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1339
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San Francisco, CA
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1488
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Scarborough, ME
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1410
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Seattle, WA
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1234
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Voorhees, NJ
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1284
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from
West Palm Beach, FL
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976
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Winston-Salem, NC
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