Breast Cancer Clinical Trial
Official title:
A Multicenter, Open-Label, Phase II Study of LEP-ETU for Efficacy and Safety in Patients With Metastatic Breast Cancer
LEP-ETU is a novel, proprietary delivery system of paclitaxel developed by NeoPharm, Inc.
Paclitaxel (currently marketed as Taxol) is an anti-microtubular network agent and is active
in a broad spectrum of malignancies. Paclitaxel has poor solubility. In order to enhance the
solubility, this drug is formulated with polyoxyethylated castor oil, which leading to
infusion-related hypersensitivity reactions. The NeoPharm LEP-ETU is formulated with a
mixture of well characterized, synthetic phospholipids and cholesterol. This design
eliminates the need for the oil. The LEP-ETU formulation has improved safety profile that is
necessary for administering higher doses than would commonly be used with Taxol. The
clinical evidence obtained from the NeoPharm Phase I study shows LEP-ETU is better tolerated
than Taxol, as indicated by a higher maximum-tolerated dose (MTD). The current Phase II
study is designed to accomplish the following objectives:
1. Assess the Overall Response Rate (ORR) of patients with metastatic breast cancer after
administered over 90 minutes at the dose of 275 mg/m2 LEP-ETU
2. To evaluate the Progression-Free Survival (PFS)
3. To evaluate the safety of LEP-ETU at 275 mg/m2 level, in particular peripheral
neuropathy
4. To evaluate the Overall Survival (OS)
n/a
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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