drugset / Trial / NCT00306631
A Study to Determine the Antitumor Activity and Evaluate the Safety of MKC-1
Non-randomizedSingle-groupOpen-labelTreatment
Summary
This phase 2 study will determine the antitumor activity, based on the objective rate, of oral MKC-1, administered twice daily for 14 consecutive days every 4 weeks, in patients with advanced or metastatic breast carcinoma. The study will also evaluate the safety and response duration in patients, time to tumor progression, and overall survival in patients following MKC-1 therapy.
Timeline
- Start
- 2006-01
- Primary completion
- 2008-04
- Completion
- 2008-11
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | MKC-1 | Small molecule | 30 mg | Oral |
| Subject | MKC-1 | Small molecule | 100 mg | Oral |