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

NCT00287885

NCT00287885
Completed Phase 1

Who may be able to join

Who might be able to join this trial:

  • You have been diagnosed with an advanced gynecological cancer (such as ovarian, cervical, or uterine cancer) that has been confirmed by a tissue sample (biopsy), and the cancer has not responded well to previous treatments.
  • You have already received chemotherapy, and your cancer has either come back or did not fully go away after treatment.
  • You have at least one area of cancer that can be measured on a scan, OR you have cancer that shows up on blood tests (a protein called CA-125 is above 50 units/ml on two tests taken at least one week apart).
  • You are generally well enough to carry out light activity and care for yourself (your doctor will assess this using a standard scale called ECOG, and you need to score 0 or 1).
  • You are at least 18 years old.
  • Your blood, liver, and kidney test results are within acceptable ranges, checked within the past 4 weeks before joining.
  • You have not had another cancer in the past 5 years, except for certain minor skin cancers or a very early-stage cervical condition.
  • You have not received hormonal or immune therapy in the last 2 weeks, or chemotherapy/radiation in the last 4 weeks (some specific drugs require a 6-week gap — confirm with trial site).
  • You are willing and able to sign a written consent form confirming you understand the experimental nature of the treatment and its possible risks.

Who may not be able to join:

  • You are currently pregnant or breastfeeding, as the study drugs could be harmful to an unborn baby or infant.
  • You are able to become pregnant but are unwilling to use reliable contraception (preferably a barrier method such as condoms) during the trial.
  • You have a history of a heart attack, heart failure, or significant heart valve or blood flow problems in the heart.
  • You have cancer that has spread to the brain.
  • You have moderate to severe nerve damage in your hands or feet (such as numbness, tingling, or pain — confirm level with trial site).
  • You have previously had a serious allergic reaction to docetaxel (a chemotherapy drug) or to certain other medicines containing a substance called polysorbate 80.

Important: Always verify eligibility with the trial site directly before applying.

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

Phase 1: approximately ~10% 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 1
Sponsor
Masonic Cancer Center, University of Minnesota
Registry
clinicaltrials_gov
Start date
1 March 2004
Est. completion
1 December 2008

Primary endpoints

Maximum Tolerated Dose

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