Safety and Efficacy Study of Abraxane Plus Gemcitabine in Chinese Patients With Metastatic Pancreatic Cancer
This trial is active, not recruiting.
|Start date||December 2013|
|End date||June 2015|
|Trial size||83 participants|
|Trial identifier||NCT02017015, ABI-007-PANC-001|
The purpose of this study is to determine the safety and efficacy of Abraxane combined with Gemcitabine in Chinese patients with metastatic pancreatic cancer.
|United States||No locations recruiting|
|Other countries||No locations recruiting|
|Beijing, PR, China||Beijing Cancer Hospital||no longer recruiting|
|Beijing, China||307 Hospital of Chinese PLA||no longer recruiting|
|Beijing, China||Chinese PLA General Hospital||no longer recruiting|
|Beijing, China||Peking Union Medical College Hospital||no longer recruiting|
|Guangzhou, China||Sun Yat-sen University Cancer Center||no longer recruiting|
|Hangzhou, Zhejiang, China||Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University||no longer recruiting|
|Hangzhou, Zhejiang, China||The First Affiliated Hospital of Medical School of Zhejiang University||no longer recruiting|
|Hangzhou, China||Zhejiang Cancer Hospital||no longer recruiting|
|Harbin, Heilongjiang, China||Harbin Medical University Tumor Hospital||no longer recruiting|
|Nanjing, China||Jiangsu Province Hospital/ The First Hospital affiliated with Nanjing Medical University||no longer recruiting|
|Shanghai, China||Fudan University Shanghai Cancer Center||no longer recruiting|
|Shanghai, China||Shanghai First People's Hospital||no longer recruiting|
|Tianjin, China||Tianjin Medical University Cancer Institute and Hospital||no longer recruiting|
|Xi'an, China||Xijing Hospital||no longer recruiting|
|Zhengzhou, China||Henan Cancer Hospital||no longer recruiting|
|Endpoint classification||efficacy study|
|Intervention model||single group assignment|
Objective Response Rate
time frame: 18 months
Duration of response according to RECIST 1.0 guidelines
time frame: 18 months
time frame: 3 years
time frame: 19 months
Male or female participants at least 18 years old.
- Patient has definitive histologically or cytologically confirmed metastatic pancreatic adenocarcinoma (Islet cell neoplasms are excluded) that is measurable by RECIST
- Patients must have received no previous radiotherapy, surgery, chemotherapy or investigational therapy for the treatment of metastatic pancreatic cancer. Prior treatment with 5-FU or gemcitabine administered as a radiation sensitizer in the adjuvant setting is allowed, provided at least 6 months have elapsed since completion of the last dose and no lingering toxicities are present. Patients having received cytotoxic doses of gemcitabine or any other chemotherapy in the adjuvant setting are not eligible for this study
- Patient has a Karnofsky performance status (KPS) ≥ 70
- Initial diagnosis of metastatic disease must have occurred ≤ 6 weeks prior to starting Cycle 1 Day 1. NOTE: the clock for this time interval starts with the date of last evaluation confirming pancreatic metastatic disease (either biopsy or imaging results)
- Patients should be asymptomatic for jaundice prior to Cycle 1 Day 1. Significant or symptomatic amounts of ascites should be drained prior to Cycle 1 Day 1. Pain symptoms should be stable and should not require modifications in analgesic management prior to Cycle 1 Day 1
- Patient has adequate blood counts at Screening (obtained ≤ 14 days prior to starting Cycle 1 Day 1):
- Absolute neutrophil count (ANC) ≥ 1.5 × 10^9/L;
- Platelet count ≥ 100,000/mm3 (100 × 10^9/L);
- Hemoglobin (Hgb) ≥ 9 g/dL
- Patient has the following blood chemistry levels at Screening (obtained ≤ 14 days prior to starting Cycle 1 Day 1):
- Aspartate Aminotransferase (SGOT) and Alanine Transaminase (SGPT) are ≤ 2.5 × upper limit of normal range , unless liver metastases are clearly present, then ≤ 5 × upper limit of normal range is allowed
- Total bilirubin ≤ upper limit of normal range
- Serum creatinine within normal limits or calculated clearance ≥ 60 mL/min/1.73 m2 for patients with serum creatinine levels above or below the institutional normal value. If using creatinine clearance, actual body weight should be used for calculating creatinine clearance (eg, using the Cockroft-Gault formula). For patients with a Body Mass Index (BMI) > 30 kg/m2, lean body weight should be used instead.
- Patient has acceptable coagulation studies (obtained ≤14 days prior to starting Cycle 1 Day 1) as demonstrated by prothrombin time (PT) and partial thromboplastin time (PTT) within normal limits (±15%). (See also Section 6.2 for Screening PT/PTT analysis).
- Patient has no clinically significant abnormalities in urinalysis results (obtained ≤14 days prior to starting Cycle 1 Day 1).
- Male or non-pregnant and non-lactating female, and ≥ 18 years of age at the time of signing the informed consent document.
- If a female patient is of child-bearing potential, as evidenced by regular menstrual periods, she must have a negative pregnancy test (e.g. serum β-hCG) documented prior to the first administration of study drug.
- If sexually active, the patient must agree to use contraception considered adequate and appropriate by the Investigator during the period of administration of study drug. In addition, male and female patients must utilize contraception after the end of treatment as recommended in the product's Prescribing Information provided in the study manual.
- Patient has been informed about the nature of the study, and has agreed to participate in the study, and signed the Informed Consent Form prior to participation in any study-related activities.
- Able to adhere to the study visit schedule and other protocol requirements.
- History of malignancy in the last 5 years (including chronic leukemias). Patients with prior history of in situ cancer or basal or squamous cell skin cancer are eligible. Patients with other malignancies are eligible if they were cured by surgery alone or surgery plus radiotherapy and have been continuously disease-free for at least 5 years.
- Patient has active, uncontrolled bacterial, viral, or fungal infection(s) requiring systemic therapy.
- Patient has known infection with Human Immunodefiency Virus, and/or active infection with hepatitis B, or hepatitis C (patients with known historical infection with hepatitis B or C should be discussed with the Sponsor).
- Patient has undergone major surgery, other than diagnostic surgery (ie, surgery done to obtain a biopsy for diagnosis without removal of an organ), within 4 weeks prior to Day 1 of treatment in this study.
- Patient that has a history of a myocardial infarction, severe/unstable angina pectoris, coronary/peripheral artery bypass graft, New York Heart Association (NYHA) Class III-IV heart failure, uncontrolled hypertension, clinically significant cardiac dysrhythmia or electrocardiogram (ECG) abnormality, cerebrovascular accident, transient ischemic attack, seizure disorder or clinically significant cardiac dysrhythmia or electrocardiogram (ECG) abnormality, within 6 months prior to Cycle 1 Day 1 9. Patient has a history of allergy or hypersensitivity to any of the study drugs or any of their excipients, or the patient exhibits any of the events outlined in the Contraindications or Special Warnings and Precautions sections of the product or comparator Prescribing Information.
- History of connective tissue disorders (eg, lupus, scleroderma, arteritis nodosa).
- Patients with a history of interstitial lung disease , history of slowly progressive dyspnea and unproductive cough, sarcoidosis, silicosis, idiopathic pulmonary fibrosis, pulmonary hypersensitivity pneumonitis or multiple allergies.
- Patient has any condition, including serious medical risk factors, medical conditions, laboratory abnormalities or psychiatric disorders, which could compromise the patient's safety or the study data integrity.
- Patient is enrolled in any other clinical protocol or investigational trial with an interventional agent or assessments that may interfere with study procedures.
- Patient is unwilling or unable to comply with study procedures, or is planning to take vacation for 7 or more consecutive days during the treatment phase of the study.
|Official title||A PHASE 2, MULTI-CENTER STUDY TO EVALUATE THE SAFETY AND EFFICACY OF ABI-007 PLUS GEMCITABINE IN CHINESE PATEINTS WITH METASTATIC PANCREATIC ADENOCARCINOMA|
|Description||This is a Phase 2 trial in China to evaluate the safety and efficacy of the combination of Abraxane and gemcitabine administered in patients diagnosed with metastatic pancreatic adenocarcinoma. Approximately 82-246 patients are planned to be accrued. This study is designed to be a Chinese bridging study to complement the Global pivotal study (CA-046). The study consists of three parts: (1) Dose evaluation; (2) Single arm to evaluate efficacy following an optimal Simon two-stage design; and (3) Randomized 2-arm to evaluate the efficacy and safety of Abraxane plus gemcitabine versus gemcitabine alone. These 3 parts will be carried out sequentially. The Part 3 randomized 2-arm portion will only be carried out if deemed necessary per protocol.|
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