CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 332 enrolled
Drug / intervention
Farletuzumab +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02289950
NCT02289950Phase 2Completed

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

Eisai Inc.·interventional·Posted Nov 13, 2014·Updated Sep 2, 2021

In Brief

A Phase 2 clinical trial evaluating Farletuzumab and Placebo for Platinum-Sensitive Ovarian Cancer in First Relapse. Completed, enrolled 332 participants across 68 sites in 7 countries.

Detailed Summary

MORAb-003-011 is a global, multicenter, double-blind, randomized placebo-controlled study to assess the safety and efficacy of farletuzumab in combination with standard chemotherapy in subjects with low cancer antigen 125 (CA125) platinum-sensitive ovarian cancer in first relapse.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesBelgium, Germany, Italy, Japan, Spain, United Kingdom, United States
Collaborators--

Timeline

Phase 2CompletedFinished
201520162017201820192020202120222023202420252026
First PostedNov 13, 2014
Enrollment StartMar 19, 2015
Primary CompletionMay 31, 2019
Study CompletionAug 13, 2020
TodayJul 2, 2026
Enrollment to primary: 4.2 yearsPosted 11.6 years ago

Interventions

Farletuzumabdrug

Farletuzumab will be administered intravenously (IV) weekly

Placebodrug

Placebo will be administered intravenously (IV) weekly