CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 132 enrolled
Drug / intervention
Bevacizumab (Avastin®) +2 moredrug
Likely dose
Bevacizumab (Avastin®) 15 mg/kgfrom 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/NCT00296816
NCT00296816Phase 2Completed

A Pilot Phase II Study Evaluating the Combination of Oxaliplatin and Docetaxel With Bevacizumab as First Line Therapy in Patients With FIGO Stage IB-IV Epithelial Ovarian, Primary Peritoneal or Fallopian Tube Carcinoma

Sanofi·interventional·Posted Feb 27, 2006·Updated Aug 23, 2012

In Brief

A Phase 2 clinical trial evaluating Bevacizumab (Avastin®), Docetaxel (Taxotere®), and 1 other intervention for Ovarian Cancer. Completed, enrolled 132 participants across 1 site.

Detailed Summary

Feasibility study to assess a novel combination of cytotoxic agents, docetaxel and oxaliplatin, as first-line therapy in the treatment of ovarian cancer and the impact of angiogenesis inhibition for the progression and prognosis of ovarian cancer by concurrent addition of bevacizumab (Avastin®).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsOvarian Cancer
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedFeb 27, 2006
Enrollment StartMar 1, 2006
Primary CompletionAug 1, 2011
TodayJul 2, 2026
Enrollment to primary: 5.4 yearsPosted 20.3 years ago

Interventions

Bevacizumab (Avastin®)drug

15 mg/kg bevacizumab administered intravenously (IV) over 30 to 90 minutes on Day 1 of every 3 week cycle for 12 months or until disease progression or unacceptable toxicity

Docetaxel (Taxotere®)drug

75 mg/m\^2 docetaxel was administered IV over 1 hour on Day 1 of every 3 week cycle for 6 cycles or until disease progression or unacceptable toxicity

Oxaliplatin (Eloxatin®)drug

85 mg/m\^2 Oxaliplatin was administered IV over 2 hours on Day 1 of every 3 week cycle for 6 cycles or until disease progression or unacceptable toxicity