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Clinical Trials/EUCTR2011-001015-32-FI
EUCTR2011-001015-32-FI
Active, not recruiting
Phase 1

A prospective randomised Phase III trial to evaluate optimal treatment duration of first-line bevacizumabin combination with carboplatin and paclitaxel in patients with primary epithelial ovarian, fallopian tube or peritoneal cancer. - The BOOST (Bevacizumab Ovarian Optimal Standard Treatment) Trial - boost

Johanna Mäenpää0 sites796 target enrollmentMarch 12, 2012

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Epithelial ovarian cancer, fallopian tube carcinoma, primary peritoneal carcinoma, FIGO Stages IIb-IV
Sponsor
Johanna Mäenpää
Enrollment
796
Status
Active, not recruiting
Last Updated
5 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 12, 2012
End Date
TBD
Last Updated
5 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
Female

Investigators

Sponsor
Johanna Mäenpää

Eligibility Criteria

Inclusion Criteria

  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1\.2 Adults (18\-64 years) yes
  • F.1\.2\.1 Number of subjects for this age range 498
  • F.1\.3 Elderly (\>\=65 years) yes
  • F.1\.3\.1 Number of subjects for this age range 298

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

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