Sorafenib/ Carboplatin/ Paclitaxel in Patients With Solid Tumors

NCT ID: NCT00606125

Last Updated: 2014-06-23

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 16 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2007-05-31
• Study Completion Date: 2009-02-28

Brief Summary

The purpose of this study is to:

1. Evaluate how the body reacts to sorafenib when taken daily in combination with paclitaxel and carboplatin,

2. Measure the blood levels of sorafenib, paclitaxel and carboplatin at specific times after taking the medication, and

3. To determine the safety of sorafenib.

Conditions

Neoplasms

Study Design

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

Study Groups

Arm 1

Group Type: EXPERIMENTAL

Nexavar (Sorafenib, BAY43-9006)

Intervention Type: DRUG

The purpose of this study is to: 1)evaluate how your body reacts to sorafenib when taken daily in combination with paclitaxel and carboplatin, 2) measure your blood levels of sorafenib, paclitaxel and carboplatin at specific times after taking the medication, and 3) to determine the safety of sorafenib.

Interventions

Nexavar (Sorafenib, BAY43-9006)

The purpose of this study is to: 1)evaluate how your body reacts to sorafenib when taken daily in combination with paclitaxel and carboplatin, 2) measure your blood levels of sorafenib, paclitaxel and carboplatin at specific times after taking the medication, and 3) to determine the safety of sorafenib.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Age > or equal to 18 years
• Histological or cytological documentation of cancer, except non small cell lung cancer
• ECOG Performance Status of 0 or 1
• Life expectancy of at least 12 weeks
• No more than two prior chemotherapy regimens
• Adequate bone marrow, liver and renal function as assessed by the following:

• Hemoglobin > or equal to 9.0 g/dL
• Absolute neutrophil count (ANC) > or equal to 1,500/mm3
• Platelet count > or equal to 100,000/mm3
• Total bilirubin < or equal to 1.25 times the ULN
• ALT and AST < or equal to 2.5 x ULN
• PT-INR/PTT < 1.5 x ULN (Patients who are being prophylactically anti coagulated with an agent such as coumadin or low molecular weight heparin or therapeutically anticoagulated with LMWH will be allowed to participate provided that they meet these criteria; in addition, these patients must be monitored at appropriate intervals throughout study)
• Women of childbearing potential must have a negative serum pregnancy test performed within 7 days prior to the start of treatment.
• Women of childbearing potential and men must agree to use adequate contraception prior to study entry and for the duration of study participation, including the 30 day period after last study drug dosing. The investigator should advise the patient regarding adequate means of contraception.
• Serum creatinine < or equal to 1.5 x upper limit of normal
• Ability to understand and willingness to sign a written informed consent. A signed informed consent must be obtained prior to any study specific procedures

Exclusion Criteria

• Clinically evident congestive heart failure > NYHA Class 2 (See Appendix 10.4)
• Serious cardiac arrhythmias (for example requiring anti-arrhythmics)
• Myocardial infarction or symptomatic coronary artery disease (severe or unstable angina) within 6 months prior to screening
• Active clinically serious infections (> Grade 2 NCI-CTC)
• Patients with history of brain metastases are eligible as long as the metastasis has been treated with either stereotactic or whole brain radiation, stereotactic gamma-knife radiosurgery or neurosurgery, patient does not require ongoing treatment with dexamethasone, the patient is not on anticoagulant therapy and whose radiographic imaging is stable ≥ 4 weeks from start of treatment. Time from brain metastasis treatment to first study treatment must meet the following criteria:

• Stereotactic or whole brain radiation, stereotactic gamma-knife radiosurgery ≥ 4 weeks from first study treatment
• Neurosurgery ≥ 24 weeks from first study treatment
• Brain biopsy ≥ 12 weeks from first study treatment
• History of organ allograft
• Uncontrolled seizure disorder. Use of cytochrome P450 enzyme-inducing antiepileptic drugs (phenytoin, carbamazepine or phenobarbital) is not allowed
• Uncontrolled hypertension defined as systolic blood pressure > 150 mmHg or diastolic pressure > 90 mmHg, despite optimal medical management
• Known human immunodeficiency virus (HIV) infection or chronic hepatitis B or C
• Peripheral neuropathy > or equal to Grade 2
• Thrombotic or embolic events (such as transient ischemic attacks, myocardial infarction, pulmonary embolus), within 6 months prior to Screening
• Pulmonary hemorrhage/bleeding event > CTCAE Grade 2 within 4 weeks of first study treatment
• Any other hemorrhage/bleeding event > CTCAE Grade 3 within 4 weeks of first study treatment
• Evidence or history of bleeding diathesis or coagulopathy
• Serious, non-healing wound, ulcer, or bone fracture
• Patients undergoing renal dialysis
• Major surgery, open biopsy or significant traumatic injury within 4 weeks of first study treatment
• Previous cancer EXCEPT cervical cancer in-situ, treated basal cell carcinoma, superficial bladder tumors [Ta and Tis] or any cancer curatively treated > 3 years prior to first study treatment
• Non small cell lung cancer
• Ongoing substance abuse, medical, psychological or social conditions that may interfere with the patient's participation in the study or evaluation of the study results
• Pregnant or breast-feeding patients.
• Known or suspected allergy to the investigational agent or any agent given in association with this trial
• Any condition that is unstable or could jeopardize the safety of the patient and their compliance in the study
• Any condition that impairs patient's ability to swallow whole pills
• Any malabsorption condition

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

Sponsors

Bayer

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Bayer Study Director

Role: STUDY_DIRECTOR

Bayer

Locations

New Haven, Connecticut, United States

San Antonio, Texas, United States

Countries

United States

Other Identifiers

11988

Identifier Type: -

Identifier Source: org_study_id