Safety and Tolerability Study of TAK-165 in Subjects With Tumors Expressing HER2

NCT ID: NCT00034281

Last Updated: 2012-02-02

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 16 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2002-06-30
• Study Completion Date: 2003-09-30

Brief Summary

The purpose of this study is to investigate a safe dose of TAK-165, once daily (QD), in patients with HER2-tumor expression.

Detailed Description

The human epidermal growth factor receptor 2 (HER2) is a member of the Type 1 family of growth factor tyrosine kinases. HER2 forms hetero- and homo-dimers with other members of this family of tyrosine kinases. As a result of dimerization at the cell surface, intracellular signal transduction is initiated, resulting in cell proliferation.

HER2 expression has been observed in a variety of human tumors including breast cancer, non-small cell lung cancer, prostate cancer, pancreatic cancer, renal cell cancer, and ovarian cancer. HER2 overexpression is associated with clinically more aggressive breast cancer, and is an independent predictor of poor prognosis in patients with breast cancer.

TAK-165 is an active and selective inhibitor of tyrosine kinase activity of HER2 being developed for patients with lower levels of HER2 expression. This study will seek to determine the safety, tolerability, maximum tolerated dose and pharmacokinetics of TAK-165 administered to subjects with tumors known to express HER2.

The total duration of the study will be at minimum 8 weeks, or 56 Days. Subjects without progressive disease after 8 weeks may continue to receive study drug, provided that they do not meet criteria for withdrawal.

Conditions

Breast Neoplasm; Pancreatic Neoplasm; Lung Neoplasm; Ovarian Neoplasm; Renal Neoplasm

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

TAK-165 QD

Group Type: EXPERIMENTAL

TAK-165

Intervention Type: DRUG

Starting dose of TAK-165 10 mg, tablets, orally, once daily with dose escalation to tolerability for 56 days.

Interventions

TAK-165

Starting dose of TAK-165 10 mg, tablets, orally, once daily with dose escalation to tolerability for 56 days.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Have advanced or metastatic cancer which is refractory to standard therapy or subjects for whom there is no known effective therapy.
• Have a histologically or cytologically proven diagnosis of a solid tumor known to express HER2.
• Have a predicted life expectancy of greater than or equal to 12 weeks.
• Have a Karnofsky Performance Status of greater than or equal to 60%
• Have recovered from toxicities of prior chemotherapy, surgery, or radiotherapy.

Exclusion Criteria

• Be pregnant or lactating. Women of childbearing potential must have a negative serum pregnancy test result within 7 days of enrollment into the study. Male and female subjects of childbearing potential (including women who have been amenorrheic for less than 1 year) must use appropriate birth control during the entire duration of the study, or the subject must be surgically sterile.
• Have symptomatic brain metastasis
• Have received any other anti-cancer treatment or investigational drug/treatment within 28 days prior to study Day 1.
• Have a history of another malignancy within the last 5 years.
• Have inadequate organ function.
• Have heart failure defined by an ejection fraction of less than or equal to 50% as measured by MUGA.
• Have Class II, III or IV symptoms of heart failure as defined by the New York Heart Association, or uncontrolled arrhythmias, or recent history of myocardial infarction or angina pectoris.
• Have a medical condition that may interfere with intake and/or absorption of the study drug (e.g., gastrectomy or resection of major portion of small intestine).
• Have any other serious disease or condition present at screening or at study Day 1 that might affect life expectancy or make it difficult to successfully manage and follow the subject according to the protocol.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Takeda

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Medical Director

Role: STUDY_DIRECTOR

Takeda

Locations

Arizona Cancer Center

Scottsdale, Arizona, United States

The Institute for Drug Development

San Antonio, Texas, United States

Brooke Army Medical Center/Drug Development Unit

San Antonio, Texas, United States

South Texas VA, Audie Murphy Division

San Antonio, Texas, United States

Countries

United States

Other Identifiers

U1111-1127-6123

Identifier Type: REGISTRY

Identifier Source: secondary_id

01-01-TL-165-001

Identifier Type: -

Identifier Source: org_study_id