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A Phase I Study of ABT-888 in Combination With Temozolomide in Cancer Patients

Breast Cancer Clinical Trial

Official title:
A Phase I Study of ABT-888 in Combination With Temozolomide (TMZ) in Subjects With Non-Hematologic Malignancies (NHM) and Metastatic Melanoma (MM)

Clinical Trial Summary

This Phase I clinical trial is studying the side effects and best dose of ABT-888 when given together with Temozolomide (chemotherapy) in treating patients with solid tumors, including metastatic melanoma (MM), BRCA deficient breast, ovarian, primary peritoneal, or fallopian tube cancer, and hepatocellular carcinoma (HCC).

Clinical Trial Description

A Phase 1, multicenter, dose-escalation study evaluating the safety and tolerability of the PARP inhibitor ABT-888 in combination with Temozolomide (TMZ) in subjects with non-hematologic malignancies (NHM), including metastatic melanoma (MM), BRCA deficient breast, ovarian, primary peritoneal, or fallopian tube cancer, and hepatocellular carcinoma (HCC). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00526617
Study type Interventional
Source AbbVie
Contact
Status Completed
Phase Phase 1
Start date August 2007
View Details
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