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An Observational Study of Avastin (Bevacizumab) in Combination With Chemotherapy as First-Line Treatment in Patients With Advanced Ovarian Cancer (OSCAR 1)

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Roche

Status

Completed

Conditions

Ovarian Cancer

Study type

Observational

Funder types

Industry

Identifiers

NCT01863693
ML28570

Details and patient eligibility

About

This multicenter, prospective, observational study will evaluate the safety and efficacy of Avastin (bevacizumab) in combination with chemotherapy as first-line treatment in patients with advanced epithelial ovarian, fallopian tube or primary peritoneal cancer in routine clinical practice. Eligible patients will be followed for approximately 15 months.

Enrollment

300 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients, >/= 18 years of age
  • Advanced (FIGO stages IIIB, IIIC and IV) epithelial ovarian, fallopian tube or primary peritoneal cancer not previously treated with chemotherapy
  • Initiating Avastin in combination with chemotherapy

Exclusion criteria

  • Contraindications, warnings and precautions for use as specified in the Avastin Summary of Product Characteristics

Trial design

300 participants in 1 patient group

Cohort

Trial contacts and locations

30

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Data sourced from clinicaltrials.gov

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