Combination Study of a New Taxane and Capecitabine in Patients With Metastatic Breast Cancer

NCT ID: NCT00327743

Last Updated: 2016-05-18

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 34 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2006-08-31
• Study Completion Date: 2009-03-31

Brief Summary

The goal of this phase I-II clinical research study is to find the highest safe dose of XRP9881 and capecitabine that can be given in combination in the treatment of metastatic breast cancer in patients who have been previously treated by taxanes and anthracyclines. The safety and effectiveness of this combination will also be studied. Patients participating in the study will be asked to give additional blood samples to look at the level of study drugs in the blood.

Conditions

Breast Cancer; Cancer

Study Design

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

Study Groups

larotaxel + Capecitabine

Group Type: EXPERIMENTAL

larotaxel

Intervention Type: DRUG

IV infusion on Day 1 of a 21-day cycle

capecitabine

Intervention Type: DRUG

oral, twice daily, Day 1-Day 14 of a 21-day cycle

Interventions

larotaxel

IV infusion on Day 1 of a 21-day cycle

Intervention Type: DRUG

capecitabine

oral, twice daily, Day 1-Day 14 of a 21-day cycle

Intervention Type: DRUG

Other Intervention Names

XRP9881

Eligibility Criteria

Inclusion Criteria

• Histologically or cytologically proven diagnosis of breast adenocarcinoma that is now metastatic or locally recurrent and inoperable with curative intent.
• Prior treatment with a standard regimen of anthracycline and taxane.
• Female patients at least 18 years old.
• Eastern Cooperative Oncology Group (ECOG) performance status (PS): 0-2
• Adequate organ and bone marrow function
• Measurable disease by Response Evaluation Criteria in Solid Tumors (RECIST) criteria (For the part I component, patients with non-measurable disease are accepted.)
• Resolution of all clinically significant toxic effects
• Completion of all prior therapy ≥ 3 weeks prior to registration. Patients on bisphosphonate therapy may continue such therapy.
• Patients must be either post-menopausal, surgically sterile, or using effective contraception.
• Willing and able to comply with study procedures and sign informed consent

Exclusion Criteria

• History of any second malignancy within the last 5 years (except adequately treated basal cell or squamous cell skin cancer, or in situ carcinoma of the cervix uteri).
• Patients receiving more than one adjuvant regimen or more than one metastatic regimen
• Known brain or leptomeningeal disease.
• Concurrent treatment on another clinical trial or with any other cancer therapy including chemotherapy, biological therapy, hormonal therapy, radiotherapy, chemoembolization therapy, cryotherapy, targeted non-cytotoxic therapies, or patients planning to receive these treatments during the study.
• Prior treatment with capecitabine, XRP9881, or any investigational chemotherapy.
• History of hypersensitivity to taxanes, Polysorbate-80, or to compounds with similar chemical structures. Patients with known intolerance to fluoropyrimidines or patients with known dihydropyrimidine dehydrogenase (DPD) deficiency.
• Concurrent treatment with potent inhibitors of cytochrome P450 3A4, or patients planning to receive these treatments. For patients who were receiving treatment with such agents, a one-week washout period is required prior to registration.
• Peripheral neuropathy grade ≥ 2.
• Any of the following within the 6 months prior to registration: myocardial infarction, severe/unstable angina, coronary/peripheral artery bypass graft surgery, clinically symptomatic and uncontrolled cardiovascular disease, or clinically significant cardiac arrhythmias (grade 3-4).
• History of inflammatory bowel disease or chronic diarrhea.
• Lack of physical integrity of the upper gastrointestinal tract, malabsorption syndrome, or inability to take oral medication.
• Other severe acute or chronic medical or psychiatric condition, or significant laboratory abnormality requiring further investigation or that may cause undue risk for the patient's safety.
• Known human immunodeficiency virus (HIV) infection requiring treatment or acquired immunodeficiency-syndrome (AIDS)-related illness.
• Patients who are pregnant or breastfeeding.

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

Sponsors

Sanofi

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

ICD

Role: STUDY_DIRECTOR

Sanofi

Locations

Sanofi-Aventis Administrative Office

Bridgewater, New Jersey, United States

Sanofi-Aventis Administrative Office

Paris, , France

Countries

United States; France

Other Identifiers

EudraCT:2006-006474-21

Identifier Type: -

Identifier Source: secondary_id

TCD6511

Identifier Type: -

Identifier Source: org_study_id