Study of Cipatinib in Patients With HER2 Positive or Uncertain Advanced Breast Cancer

NCT ID: NCT01301911

Last Updated: 2012-12-21

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE1
• Total Enrollment: 26 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-01-31
• Study Completion Date: 2012-11-30

Brief Summary

Cipatinib is an oral tyrosine kinase inhibitor targeting both HER-1 and HER-2 receptors. This study is designed to evaluate the safety and tolerability of cipatinib in patients with HER2 positive or uncertain advanced breast cancer:

1. To evaluate the safety and tolerability of cipatinib, and the maximum tolerated dose (MTD) and dose-limiting toxicity (DLT)

2. To determine the pharmacokinetic profile of cipatinib and its metabolites

3. To assess preliminary antitumor activity

4. To determine preliminary regimen for phase II study

5. To determine the relation of expression of HER-1 and HER-2 to the antitumor activity.

Conditions

Breast Cancer

Keywords

Breast cancer, Advanced; Cipatinib; phase I; HER2 positive or uncertain advanced breast cancer

Study Design

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

Study Groups

Cipatinib

Each subject will receive a single dose of cipatinib on treatment day 1, followed by 4-day observation period, and then will receive cipatinib once daily in cycles consisting of 21 days.

Group Type: EXPERIMENTAL

Cipatinib

Intervention Type: DRUG

Cipatinib either at 200, 400, 800, 1200, 1400, 1600 or 1800 mg, p.o. once daily

Interventions

Cipatinib

Cipatinib either at 200, 400, 800, 1200, 1400, 1600 or 1800 mg, p.o. once daily

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Aged ≥ 18 and ≤ 65 years.
• ECOG performance status of 0 to 1.
• Life expectancy of more than 3 months.
• Histologically or cytologic confirmed HER2 positive or uncertain advanced breast cancer that is not curable with available therapies.
• Screening laboratory values within the following parameters:

• ANC: ≥ 1.5 x 109/L
• Platelet count: ≥ 100 x 109/L
• Hemoglobin: ≥ 9.0 g/dL
• Serum albumin: ≥ 2.5 g/dL
• Total bilirubin: ≤ 1.5 x upper limit of normal, ULN
• ALT and AST: ≤ 1.5 x ULN
• Serum creatinine: ≤ 1.0 x ULN
• Creatinie clearnce rate: ≥ 50 mL/min
• Cholesterol≤7.75 mmol/L and triglyceride≤2.5 x ULN
• LVEF: ≥ 50%
• QTcF: < 470 ms
• Recovery from all clinically significant AEs related to prior therapies. Duration from the latest therapy is more than 6 weeks for nitroso or mitomycin, or more than 4 weeks for operation, radiotherapy, cytotoxic agents or molecular targeting.
• Ability or willingness to swallow tablets, no dysfunction of gastrointestinal absorption.
• All subjects who are not surgically sterile or postmenopausal must agree and commit to the use of a reliable method of birth control for the duration of the study and for 6 months after the last dose of test article. For women of child bearing potential, a negative urine or serum pregnancy test result before initiating cipatinib.
• Signed informed consent.

Exclusion Criteria

• Subjects with third space fluid that can not be controled by drainage or other methods.
• Steroid treatment for more than 50 days, or in need of long-term use of steroids.
• Subjects with uncontrol hypokalemia and hypomagniesemia before study entry.
• Subjects can not interrupt the using of the drugs that may cause QT prolongation during study.
• Subjects with meningioma, or with active central nervous system metastases as indicated by clinical symptoms.
• Subjects with liver metastases which ALT or AST > 1.5 x ULN.
• Treated or treating with EGFR or HER2 TKIs before study entry.
• Receiving any other antitumor therapy.
• Less than 4 weeks from the last clinical trial.
• Pregnant or breastfeeding women.
• Known history of hypersensitivity to cipatinib or any of it components.
• Ongoing infection (determined by investigator).
• Subjects had any heart disease: coronary artery disease, arrhythmia need to treat, heart failure, LVEF < 50%, and any other heart disease that is determined as unfit for this study by investigator, etc.
• Evidence of significant medical illness that in the investigator's judgment will substantially increase the risk associated with the subject's participation in and completion of the study. Examples include, but are not limited to, hypertension, severe diabetes, or thyroid disease.
• Known history of neurological or psychiatric disease, including epilepsy or dementia.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: Yes

Sponsors

Chinese Academy of Medical Sciences

OTHER

Sponsor Role: collaborator

Jiangsu HengRui Medicine Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Cancer Institute and Hospital, Chinese Academy of Medical Sciences

Beijing, Beijing Municipality, China

Countries

China

Other Identifiers

XPTN-Ia-1.0

Identifier Type: -

Identifier Source: org_study_id