Recruitment

Recruitment Status
Active, not recruiting
Estimated Enrollment
90

Summary

Conditions
  • Ovarian Epithelial Cancer
  • Ovarian Neoplasms
Type
Interventional
Phase
Phase 2
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 125 years
Gender
Only males

Description

The purpose of this study is to determine whether DCVAC/OvCa added to Standard of Care chemotherapy (carboplatin plus paclitaxel as first line chemotherapy) may result in prolongation of progression free survival (PFS).

The purpose of this study is to determine whether DCVAC/OvCa added to Standard of Care chemotherapy (carboplatin plus paclitaxel as first line chemotherapy) may result in prolongation of progression free survival (PFS).

Tracking Information

NCT #
NCT02107937
Collaborators
Not Provided
Investigators
Study Director: Harald Fricke, MD, PhD Sotio a.s.