NCT Number: NCT00051948
TLK286 in Combination With Paraplatin (Carboplatin) in Recurrent Ovarian Cancer
This is a dose-ranging, open label, Phase 1-2a study of TLK286 in combination with Paraplatin (carboplatin) in patients with recurrent ovarian cancer.
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Conditions
Age range
18 year and older
Sex eligibility
Female
Study type
Interventional
Phase
Phase 1 / Phase 2
Primary location
Santa Monica Hematology/Oncology Consultants, Santa Monica, California, United States
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Histologically or cytologically confirmed diagnosis of epithelial cancer of the ovary, fallopian tube, or primary peritoneal cancer
- Recurrent ovarian cancer or persistent disease following primary treatment
- At least one, but no more than four, prior chemotherapy regimens (all platinum-containing counted as one)
- At least 18 years of age
Exclusion criteria
- Pregnant or lactating women
- History of prior malignancy except for adequately treated carcinoma in situ of the uterine cervix, basal cell or squamous cell skin cancer, or other cancer for which patient has been disease-free for at least 2 years
- Known leptomeningeal metastases or carcinomatous meningitis
- Having received whole pelvis radiation therapy
Treatment and study plan
Sponsors and collaborators
Lead sponsor
Telik
Industry
Registry information
Official study title
Phase 1-2a Dose-Ranging Study of TLK286 in Combination With Paraplatin (Carboplatin) in Recurrent Ovarian Cancer
Important dates
- Study start
- 2003
- Primary completion
- 2005
- Study completion
- 2005
- First posted
- Jan 22, 2003
- Registry last updated
- Jul 25, 2011
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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