Bevacizumab in Treating Patients With Persistent or Recurrent Cancer of the Cervix

Part of paid clinical trials in Philadelphia, Pennsylvania.

Sponsor
National Cancer Institute (NCI)
Study ID
NCT00025233
Phase
PHASE2
Status
Completed

Conditions

  • Cervical Squamous Cell Carcinoma
  • Recurrent Cervical Cancer

Eligibility Criteria

Sex
FEMALE
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • bevacizumab — BIOLOGICAL
    Given IV
  • laboratory biomarker analysis — OTHER
    Correlative studies

Study Details

This phase II trial is to see if bevacizumab works in treating patients who have persistent or recurrent cancer of the cervix. Monoclonal antibodies, such as bevacizumab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or deliver cancer-killing substances to them.

Key Dates

First listed
Jan 27, 2003
Start date
Apr 30, 2002
Status verified
Jul 2019
Primary completion
Jul 31, 2009
Completion
Jul 31, 2009

Study Design

Enrollment
50 participants (actual)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: Treatment (bevacizumab)
    Patients receive bevacizumab IV over 30-90 minutes on day 1. Courses repeat every 3 weeks in the absence of disease progression or unacceptable toxicity.

Primary Outcome Measure

Progression-free Survival Greater Than 6 Months [ Time Frame: Every other 3-week treatment cycle for 6 months ]

Locations (1)

FacilityCityStateZIPSite coordinators
Gynecologic Oncology GroupPhiladelphiaPennsylvania19103-

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Gynecologic Oncology Group· Philadelphia, PA

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