TLK286 in Combination With Doxil in Platinum Refractory or Resistant Ovarian Cancer

NCT00052065CompletedPHASE1, PHASE2INTERVENTIONAL

Summary

Key Facts

Lead Sponsor

Telik

Enrollment

28

Start Date

2003-02-01

Completion Date

2006-03-01

Study Type

INTERVENTIONAL

Official Title

Phase 1-2a Dose-Ranging Study of TLK286 in Combination With Doxil in Platinum Refractory or Resistant Ovarian Cancer

Interventions

TLK286

Conditions

Ovarian Neoplasms

Eligibility

Age Range

18 Years+

Sex

FEMALE

Inclusion Criteria

* Histologically or cytologically confirmed diagnosis of epithelial cancer of the ovary, fallopian tube cancer or primary peritoneal cancer
* Recurrent epithelial ovarian cancer or persistent disease following primary treatment
* At least one, but no more than four, prior platinum-containing chemotherapy regimens
* At least one prior taxane-containing regimen

Exclusion Criteria

* A 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 the patient has been disease-free for 2 years
* Known leptomeningeal metastases or carcinomatous meningitis
* Have received prior Doxil or other liposomal doxorubicin
* Having received whole pelvis radiation therapy

Locations

M.D. Anderson Cancer Center, Houston, United States

TLK286 in Combination With Doxil in Platinum Refractory or Resistant Ovarian Cancer