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Terminated Phase 3 Interventional

AMG 386 (Trebananib) in Ovarian Cancer (TRINOVA-2)

ClinicalTrials.gov ID: NCT01281254

Public ClinicalTrials.gov record NCT01281254. 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 21, 2026, 5:44 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 Phase 3, Randomized, Double-Blind Trial of Pegylated Liposomal Doxorubicin (PLD) Plus AMG 386 or Placebo in Women With Recurrent Partially Platinum Sensitive or Resistant Epithelial Ovarian, Primary Peritoneal, or Fallopian Tube Cancer

Brief summary

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

To determine if AMG 386 plus pegylated liposomal doxorubicin (PLD) is superior to placebo plus PLD as measured by progression-free survival (PFS) The hypothesis for this study is that AMG 386 plus PLD will prolong PFS compared to placebo plus PLD in women with recurrent partially platinum sensitive or resistant epithelial ovarian, primary peritoneal or fallopian tube cancer.

Study identification

NCT ID
NCT01281254
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Amgen
Industry
Enrollment
223 participants

Conditions and interventions

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
Apr 18, 2011 (Actual)
Primary completion
Aug 29, 2014 (Actual)
Completion
Apr 19, 2017 (Actual)
Last update posted
Dec 2, 2017

2011 – 2017

United States locations

U.S. sites
21
U.S. states
13
U.S. cities
21
Facility City State ZIP Site status
Research Site Los Angeles California 90027 —
Research Site San Francisco California 94143 —
Research Site Norwalk Connecticut 06856 —
Research Site Stamford Connecticut 06902 —
Research Site Orlando Florida 32806 —
Research Site Tampa Florida 33612 —
Research Site Evanston Illinois 60201 —
Research Site Saint Louis Park Minnesota 55426 —
Research Site New York New York 10029 —
Research Site Asheville North Carolina 28806 —
Research Site Durham North Carolina 27710 —
Research Site Winston-Salem North Carolina 27103 —
Research Site Bismarck North Dakota 58501 —
Research Site Abington Pennsylvania 19001 —
Research Site Sioux Falls South Dakota 57104 —
Research Site Fort Sam Houston Texas 78234 —
Research Site San Antonio Texas 78229 —
Research Site Annandale Virginia 22003 —
Research Site Green Bay Wisconsin 54301 —
Research Site Milwaukee Wisconsin 53215 —
Research Site West Allis Wisconsin 53227 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 85 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01281254, 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 Dec 2, 2017 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01281254 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →