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CompletedNCT01455493Updated Aug 11, 2016

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

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

Phase
Phase 2
Study type
Interventional
Enrollment
56
Allocation
Not applicable
Ages
18 Years and older
Sex
Female
01

Study 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.

02

Conditions studied

  • Endometrial Carcinoma
03

In context

Carcinoma

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 →

Lead sponsor

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.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No

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

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
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
56 participants (actual)

Study arms

  • Experimental
    A

    Drug: GDC-0980

Interventions

  • DrugGDC-0980

    Oral daily dose

06

What researchers measure

Primary outcomes

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

    Time frame: up to approximately 23 months

  2. 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 outcomes

  1. Overall survival (OS), defined as the time from treatment initiation until death from any cause

    Time frame: up to approximately 36 months

  2. 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

  3. Incidence of adverse events

    Time frame: up to approximately 23 months

  4. Nature of adverse events

    Time frame: up to approximately 23 months

  5. Severity of adverse events

    Time frame: up to approximately 23 months

07

Study locations

28 sites
  • Phoenix, Arizona 85013, United States
  • Newport Beach, California 92663, United States
  • Orange, California 92868, United States
  • Palo Alto, California 94305, United States
  • San Francisco, California 94115, United States
  • Denver, Colorado 80220, United States
  • New Haven, Connecticut 06511, United States
  • Boca Raton, Florida 33487, United States
  • Orlando, Florida 32804, United States
  • West Palm Beach, Florida 33401, United States
  • Hinsdale, Illinois 60521, United States
  • Indianapolis, Indiana 46237, United States
  • Louisville, Kentucky 40202, United States
  • Scarborough, Maine 04074, United States
  • Baltimore, Maryland 21231, United States
  • Boston, Massachusetts 02115-6084, United States
  • Boston, Massachusetts 02215, United States
  • Voorhees, New Jersey 08043, United States
  • New York, New York 10016, United States
  • New York, New York 10017, United States
  • Durham, North Carolina 27710, United States
  • Winston-salem, North Carolina 27103, United States
  • Oklahoma City, Oklahoma 73104, United States
  • Abington, Pennsylvania 19001, United States
  • Pittsburgh, Pennsylvania 15213, United States
  • Salt Lake City, Utah 84112, United States
  • Seattle, Washington 98195, United States
  • Milwaukee, Wisconsin 53226, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 11, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01455493
Lead sponsor
Genentech, Inc.
Responsible party
Sponsor
First posted
Oct 20, 2011
Start date
Dec 2011
Primary completion
Mar 2013
Completion
Jan 2014
Last update
Aug 11, 2016

Study contacts

Clinical Trials
study director · Genentech, Inc.
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

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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