An Open Label Extension Study of the Efficacy of MORAb-003

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01018563
Recruitment Status : Completed
First Posted : November 23, 2009
Last Update Posted : December 11, 2015
Information provided by (Responsible Party):

Brief Summary:
An open label extension of the MORAb-003-002 study in order to continue the active patients in the MORAb-003-002 study on maintenance MORAb-003 infusions after the main study is closed.

Condition or disease Intervention/treatment Phase
Epithelial Ovarian Cancer Drug: MORAb-003 Phase 2

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 3 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: An Open Label Extension Study of the Efficacy of MORAb-003 in Subjects With Platinum-Sensitive Epithelial Ovarian Cancer in First Relapse
Study Start Date : November 2009
Actual Primary Completion Date : March 2013
Actual Study Completion Date : August 2013

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Ovarian Cancer
U.S. FDA Resources

Arm Intervention/treatment
Experimental: MORAb-003
Maintenance infusions of MORAb-003 every 3 weeks
Drug: MORAb-003
Dose group to be determined by dose assigned in main study and patient's weight. Intravenous infusions are given every 3 weeks.
Other Name: Farletuzumab

Primary Outcome Measures :
  1. CA125 [ Time Frame: Every 3 weeks ]

Secondary Outcome Measures :
  1. Overall response rate by Response Evaluation Criteria in Solid Tumors (RECIST) criteria [ Time Frame: Every 18 weeks ]
    Evaluation of tumor response by CT or MRI scans every 18 weeks as long as patient's condition is stable; every 9 weeks during chemotherapy, if indicated.

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Provision of Informed consent
  • Subjects must have been enrolled in and have met the inclusion/exclusion criteria of the MORAb-003-002 study.
  • Subjects must have achieved a normalization of CA 125 levels and/or CR or PR (or stable disease and an investigator's assessment of a clinical benefit) after MORAb-003 in combination with standard chemotherapy and have not yet met the criteria for disease progression during participation in the MORAb-003-002 study.
  • Subjects must be currently receiving single-agent MORAb-003 maintenance therapy.

Exclusion Criteria:

  • Subjects that discontinued the MORAb-003-002 study for any reason.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT01018563

United States, California
Sharp Memorial Hospital
Chula Vista, California, United States, 91911
United States, Texas
South Texas Oncology & Hematology
San Antonio, Texas, United States, 78229
Nationales Centrum fur Tumorerkrandungen
Heidelberg, Germany, 69120
Sponsors and Collaborators
Study Director: Susan Weil, MD Morphotek

Responsible Party: Morphotek Identifier: NCT01018563     History of Changes
Other Study ID Numbers: MORAb-003-002A
First Posted: November 23, 2009    Key Record Dates
Last Update Posted: December 11, 2015
Last Verified: November 2015

Keywords provided by Morphotek:
Extension study
Epithelial ovarian cancer

Additional relevant MeSH terms:
Ovarian Neoplasms
Neoplasms, Glandular and Epithelial
Endocrine Gland Neoplasms
Neoplasms by Site
Ovarian Diseases
Adnexal Diseases
Genital Diseases, Female
Genital Neoplasms, Female
Urogenital Neoplasms
Endocrine System Diseases
Gonadal Disorders
Neoplasms by Histologic Type