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This trial is complete. It is no longer accepting participants. Results may be available on ClinicalTrials.gov.

NCT01146795

NCT01146795
Completed Phase 2

Who may be able to join

Who might be able to join this trial:

  • You have been diagnosed with, or are suspected to have, advanced-stage ovarian cancer, fallopian tube cancer, or primary peritoneal cancer (advanced stage means it has spread widely in the abdomen or beyond).
  • Your cancer has been confirmed or is strongly suspected to be a type called "epithelial" cancer through a tissue or fluid sample.
  • You are reasonably active and able to care for yourself, or only have mild limitations in daily activity (confirm with trial site).
  • If you have previously been treated with a certain type of chemotherapy drug called an anthracycline, you must have had a recent heart scan before joining.
  • Your blood counts are healthy enough — including white blood cells, platelets, and red blood cells — at levels the trial team considers safe.
  • Your kidneys are functioning well enough, based on blood test results.
  • Your liver is functioning well enough, based on blood test results.
  • You do not have significant nerve damage (such as numbness or weakness) beyond a mild level.
  • Your blood clotting levels are within an acceptable range (or stable if you are on a blood-thinning medication like warfarin).
  • Your cancer can be measured on scans or tests.
  • A specific blood marker for ovarian cancer (called CA-125) is at or above a certain level (70 units/mL).
  • A specialist surgeon has assessed you and believes you are likely fit enough to have surgery to remove as much cancer as possible after 3 rounds of chemotherapy.
  • You have signed a consent form agreeing to take part and allowing your health information to be used.
  • You may be taking hormone replacement therapy (estrogen with or without progestin).

Who may not be able to join:

  • You have already had surgery related to your cancer, other than a small biopsy or fluid sample.
  • You have already received chemotherapy, immunotherapy, radiation, hormone therapy, or biological therapy for this cancer.
  • Your cancer is a borderline type, a returning (recurrent) cancer, or a non-epithelial type of ovarian cancer.
  • A certain ratio between two blood markers (CA-125 and CEA) is below a specific level (confirm with trial site).
  • You have had another type of cancer (other than certain common skin cancers) within the last five years.
  • You have active hepatitis or severe liver disease.
  • You have a serious wound, ulcer, or bone fracture that is not healing, or you have had an abdominal fistula or internal abdominal infection in the last 6 months.
  • You have a history of a hole or tear forming in your bowel or digestive tract (gastrointestinal perforation).
  • There is unexplained free air (gas) inside your abdomen showing on scans.
  • You have signs of a blocked bowel, or you are receiving nutrition through a tube or a drip.
  • You have active bleeding, a bleeding disorder, or a tumor that is growing into or around major blood vessels.
  • You have a brain tumor, poorly controlled seizures, brain metastases (cancer that has spread to the brain and is not fully treated), or you have had a stroke or related brain event within the last 6 months.
  • You have significant heart or blood pressure problems, including uncontrolled high blood pressure, a recent heart attack or unstable chest pain (within the last 6 months), moderate-to-severe heart failure, serious irregular heartbeat requiring medication, or significant disease in the blood vessels of your legs or arms.
  • You have had a stroke within the last 6 months.
  • You have a known allergy to bevacizumab or similar laboratory-made antibody drugs (confirm with trial site).
  • You have a significant amount of protein in your urine, based on a urine test.
  • You have had a severe high blood pressure crisis or high-blood-pressure-related brain swelling.
  • You have coughed up a meaningful amount of blood (roughly half a teaspoon or more) within the last month.
  • You have had a major operation, significant injury, or open biopsy within 28 days before starting the study drug bevacizumab, or you are expected to need major surgery during the trial; or you have had a needle (core) biopsy within 7 days before starting bevacizumab.
  • Your general health and activity level is severely limited (Performance Status Grade 3 or

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.

Trial details

Status
Completed
Phase
Phase 2
Sponsor
Jason D. Wright
Registry
clinicaltrials_gov
Start date
17 May 2010
Est. completion
13 April 2015

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Number of Protocol Defined Adverse Events in Patients Receiving Neoadjuvant Carboplatin, Paclitaxel, and Bevacizumab

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 30 June 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

View original record on ClinicalTrials.gov