Ovarian Cancer Clinical Trial

Gemzar (Gemcitabine) and Alimta (Pemetrexed) in the Treatment of Patients With Recurrent Platinum-Sensitive and Platinum-Resistant Ovarian or Peritoneal Cancer

Summary

This study hopes to evaluate whether the combination of Gemzar plus Alimta will have any beneficial effects for patients with recurrent platinum-sensitive or platinum-resistant ovarian or peritoneal cancer. Treatments are weekly for two weeks, with the 3rd week off and will be repeated every 21 days. Side effects and the overall safety of the treatment will also be monitored and evaluated. In addition, a Quality of Life questionnaire is part of this study to help measure patient perceived benefits or drawbacks to this treatment regimen.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Patients must have disease that can be measured.
Patients must meet criteria for either platinum-resistant or platinum-sensitive ovarian or peritoneal cancer.
Patients may only have had one prior platinum-based chemotherapy regimen.
Patients must be willing and able to stop all aspirin and NSAID medications immediately before and for a time after each treatment cycle (approx. 5-8 days)
Patients must have normal kidney function.

Exclusion Criteria:

Patients may not have a Low Malignant Potential or Borderline Ovarian Tumor.
Patients may not have received pelvic or abdominal radiotherapy.
Patients must not have evidence of or received treatment for another cancer within the last 5 years.
Patients must not have been diagnosed with a heart attack in the last 6 months.
Patients who are unwilling or unable to take folic acid tablets, vitamin B12 injections or dexamethasone tablets.

Study is for people with:

Ovarian Cancer

Phase:

Phase 2

Study ID:

NCT00055432

Recruitment Status:

Terminated

Sponsor:

Eli Lilly and Company

Check Your Eligibility

Let’s see if you might be eligible for this study.

What is your age and gender ?

Submit

There is 1 Location for this study

See Locations Near You

For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-285-4559) or speak with your personal physician.
Atlanta Georgia, , United States

How clear is this clinincal trial information?

Study is for people with:

Ovarian Cancer

Phase:

Phase 2

Study ID:

NCT00055432

Recruitment Status:

Terminated

Sponsor:


Eli Lilly and Company

How clear is this clinincal trial information?

×

Introducing, the Journey Bar

Use this bar to access information about the steps in your cancer journey.

Please confirm you are a US based health care provider:

Yes, I am a health care Provider No, I am not a health care provider