First Line Ovarian Cancer Treatment - Cohort Study
- Sponsor
- ARCAGY/ GINECO GROUP
- Study ID
- NCT01832415
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Bevacizumab — DRUGObservation of bevacizumab administration in first line ovarian cancer treatment
Study Details
The French cooperative group GINECO proposes to implement an observational study to describe a real situation, in daily practice tolerance and methods of administration of bevacizumab (Avastin ®)
Key Dates
- First listed
- Apr 16, 2013
- Start date
- Apr 30, 2013
- Status verified
- Mar 2016
- Primary completion
- Feb 28, 2015
- Completion
- Mar 31, 2016
Study Design
- Enrollment
- 500 participants (actual)
Arms
- Arm: Use of bevacizumab (Avastin ®) - First-line ovarian cancerPatient receiving bevacizumab in ovarian cancer first line treatment
Primary Outcome Measure
Safety according to CTCAE v4.0 criteria [ Time Frame: Patient will be followed dureing 36 months ]
Related Studies
- Study of CRX100 as Monotherapy and in Combination With Pembrolizumab in Patients With Advanced Solid MalignanciesPHASE1 · Recruiting · BioEclipse Therapeutics · Scottsdale, Arizona
- Study of Safety and Tolerability of BCA101 Monotherapy and in Combination Therapy in Patients With EGFR-driven Advanced Solid TumorsPHASE1 · Recruiting · Bicara Therapeutics · La Jolla, California
- A Study of Azenosertib (ZN-c3) in Patients With Ovarian CancerPHASE1 · Recruiting · K-Group, Beta, Inc., a wholly owned subsidiary of Zentalis Pharmaceuticals, Inc · Aurora, Colorado
- A Study Comparing Perioperative Stress Reduction vs. Standard of Care in Ovarian Cancer (PRESERVE)Recruiting · Memorial Sloan Kettering Cancer Center · Basking Ridge, New Jersey