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Cvac as Maintenance Treatment in Patients With EOC in Complete Remission Following First-Line Chemotherapy

Study:

A Randomized, Double-Blinded, Placebo-Controlled Trial of Cvac as Maintenance Treatment in Patients With Epithelial Ovarian Cancer in Complete Remission Following First-Line Chemotherapy

Rationale:

n/a

Purpose:

The purpose of this study is to determine if an investigational cell therapy called Cvac can help prevent EOC from returning when administered to patients who are in complete remission after surgical removal of their tumor followed by standard first-line chemotherapy. Following surgery and study randomization, patients will undergo leukapheresis for manufacture of the study agent and then begin first-line chemotherapy. After completion of chemotherapy and confirmation of complete remission, patients will enter the treatment phase of the study.

Study Status: Active, not recruiting

Recruiting:
n/a

Condition Intervention Phase
Epithelial Ovarian Cancer Biological: Placebo Study Agent
Biological: Cvac
Phase 2/Phase 3

Verified by Prima BioMed Ltd October, 2013

Sponsored by: Prima BioMed Ltd
Information provided by: Prima BioMed Ltd
ClinicalTrials.gov identifier: NCT01521143

Study Type: Interventional

Study Design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention

Cleveland Clinic Foundation
Cleveland, Ohio 44195
United States

n/a

This information is abridged to display results relevant only to Cleveland Clinic. To see complete record visit ClinicalTrials.gov
  Information obtained from ClinicalTrials.gov on
Link to the current ClinicalTrials.gov record.

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