Study of TPI 287 Administered Every 21 Days in Patients With Advanced Malignancies

Cortice Biosciences

Status and phase: Completed; Phase 1

Conditions: Non-Hodgkin's Lymphoma; Neoplasms; Hodgkin's Disease

Treatments: Drug: TPI 287 Injection

Study type: Interventional

Funder types: Industry

Identifiers

NCT00256191

TPI 287-02

Details and patient eligibility

About

Tapestry Pharmaceuticals, Inc. has developed a novel taxane analog, TPI 287. TPI 287 is synthetically manufactured from naturally occurring taxanes extracted from yew starting material. The synthesis involves modification to the taxane side chain to overcome multidrug resistance and to achieve mutant tubulin binding. This study will be a multi-center, dose escalation, sequential group, Phase 1 study evaluating the intravenous administration of TPI 287 on an every 21 day cycle.

Full description

The primary objective of this study is to determine the maximum tolerated dose of TPI 287 administered every 21 days for Phase II clinical trials.

Sex: All

Ages: 18 to 85 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

Patients must be/have:

• Histological evidence of malignancy
• Advanced solid tumors that have recurred or progressed following standard therapy
• Failed one prior therapy or have no standard therapy available
• Ambulatory with ECOG of 0-1 and estimated life expectancy of > 3 months
• If female, negative pregnancy test
• If of childbearing years, agree to use birth control
• If patient with prior radiation therapy for brain metastases, on steroids, must have been stable for 1 month

Exclusion criteria

Patients will be excluded if they are or have had:

• Prior radiation within 4 weeks
• Active medical condition or organ disease which may compromise safety or interfere with the study
• Clinically significant cardiac co-morbidities or pulmonary impairment
• Concomitant therapy needs
• Treated with any investigational drugs within 30 days
• Tumors involve major artery or vein
• Prior or concurrent central nervous system (CNS) disease
• Less than 4 weeks since major surgery
• Known to be positive for HIV, hepatitis B or C
• Concurrent use of aspirin
• Use of thrombolytic agents
• Uncontrolled hypertension
• Grade II-IV peripheral vascular disease
• Pregnant or lactating
• Prior allergic history to compounds of similar chemical composition
• Inpatients
• Grade II-IV peripheral neuropathy

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)