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Completed Phase 2 Interventional Results available

A Study to Assess the Efficacy and Safety of Farletuzumab (MORAb 003) in Combination With Carboplatin Plus Paclitaxel or Carboplatin Plus Pegylated Liposomal Doxorubicin (PLD) in Participants With Low CA125 Platinum-sensitive Ovarian Cancer

ClinicalTrials.gov ID: NCT02289950

Public ClinicalTrials.gov record NCT02289950. 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 Jun 25, 2026, 7:17 PM 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 Randomized, Double-Blind, Placebo-Controlled, Phase 2 Study to Assess the Efficacy and Safety of Farletuzumab (MORAb 003) in Combination With Carboplatin Plus Paclitaxel or Carboplatin Plus Pegylated Liposomal Doxorubicin (PLD) in Subjects With Low CA125 Platinum-Sensitive Ovarian Cancer

Study identification

NCT ID
NCT02289950
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Eisai Inc.
Industry
Enrollment
332 participants

Conditions and interventions

Interventions

  • Farletuzumab Drug
  • Placebo Drug

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
Mar 18, 2015
Primary completion
May 30, 2019
Completion
Aug 12, 2020
Last update posted
Sep 1, 2021

2015 – 2020

United States locations

U.S. sites
35
U.S. states
18
U.S. cities
35
Facility City State ZIP Site status
Not listed Phoenix Arizona
Not listed Los Angeles California
Not listed Orange California
Not listed Roseville California
Not listed Sacramento California
Not listed Aurora Colorado
Not listed Miami Florida
Not listed Miramar Florida
Not listed Orlando Florida
Not listed Sarasota Florida
Not listed Tampa Florida
Not listed Atlanta Georgia
Not listed Augusta Georgia
Not listed Savannah Georgia
Not listed Chicago Illinois
Not listed Lexington Kentucky
Not listed Louisville Kentucky
Not listed Baltimore Maryland
Not listed Boston Massachusetts
Not listed Detroit Michigan
Not listed Minneapolis Minnesota
Not listed Grand Island Nebraska
Not listed New York New York
Not listed Chapel Hill North Carolina
Not listed Charlotte North Carolina
Not listed Winston-Salem North Carolina
Not listed Centerville Ohio
Not listed Cincinnati Ohio
Not listed Cleveland Ohio
Not listed Columbus Ohio
Not listed Chattanooga Tennessee
Not listed Knoxville Tennessee
Not listed Austin Texas
Not listed Annandale Virginia
Not listed Charlottesville Virginia

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 33 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02289950, 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 Sep 1, 2021 · Synced Jun 25, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02289950 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →