Study of M2ES in Patients With Advanced Pancreatic Cancer After Gemcitabine Treatment Failure
Conditions
Pancreatic Cancer
Conditions: official terms
Pancreatic Neoplasms
Study Type
Interventional
Study Phase
Phase 1
Study Design
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Intervention
Name: M2ES Type: Drug
Name: M2ES Type: Drug
Name: M2ES Type: Drug
Name: M2ES 60mg Type: Drug
Overall Status
Recruiting
Summary
The purpose of this study is to evaluate the safety and tolerability and determine the recommended dosing for the treatment in patients with advanced pancreatic cancer after fist-line Gemcitabine treatment failure.
Detailed Description
To evaluate the safety and tolerability and determine the recommended dosing for the treatment in patients with advanced pancreatic cancer after fist-line Gemcitabine treatment failure.We star with the dose M2ES 15mg,then escalate to 30mg 45mg 60mg,to find the recommended dose in clinic practise.
Criteria for eligibility
Healthy Volunteers: No
Maximum Age: N/A
Minimum Age: 18 Years
Gender: Both
Criteria: Inclusion Criteria:

1. histologically or cytologically confirmed pancreatic adenocarcinoma that was not amenable to potentially curative surgery.

2. All patients must have developed progressive disease (PD) while receiving or within 6 months after discontinuing palliative gemcitabine-based chemotherapy

3. Prior radiation therapy was allowed provided that the only sites of measurable disease were not located within the radiation port.

4. 18 years of age or older

5. Karnofsky performance status (KPS) of 60-100 points

6. measurable disease as defined by Response Evaluation Criteria in Solid Tumors (RECIST) criteria

7. Adequate hematologic, renal, and hepatic function was required as deWned by the following: WBC ≥3.5×109/L, absolute neutrophil count ≥ 1.5 × 109/L, platelet count ≥100 × 109/L, hemoglobin≥9g/dL, total bilirubin ≤2.5 upper limit of normal [ULN],AST≤2.5 ULN, or≤5 ULN if there was evidence of liver metastases;alkaline phosphatase≤ 2.5 ULN, or≤ 5 ULN if there was evidence of liver Metastases creatinine clearance≤50 mL/min,

8. life expectancy of at least 12 weeks

Exclusion Criteria:

1. patients had clinically apparent CNS metastases or carcinomatous meningitis

2. another active malignancy, or any history of other malignancy within the past 5 years except for nonmelanoma skin cancer and carcinoma in situ of the cervix

3. more than 3 weeks intervals between the last administration of the prior chemotherapy regimen and study entry

4. more than 4 weeks intervals between the last administration of the targeted therapy regimen and study entry

5. major surgery within the prior 6 weeks;

6. Pregnant or lactating women

7. tumor involvement of major blood vessels

8. uncontrolled intercurrent illness

9. A history of myocardial infarction or stroke within the last 6 months, uncontrolled hypertension, unstable angina

10. clinically significant cardiac disease (eg, congestive heart failure, symptomatic coronary artery disease and cardiac arrhythmias not well controlled with medication, or myocardial infarction)

11. urine protein ≥ 500 mg in 24 hours;

12. evidence of bleeding diathesis or coagulopathy

13. Patients on therapeutic doses of low-molecular weight heparin

14. Patients who received thrombolytic agents within the previous month or who required full-dose anticoagulation.
Location
Tianjin Medical University Cancer Institute and Hospital
Tianjin, Tianjin, China
Status: Recruiting
Contact: Jihui HAO, MD - 862223359929
Start Date
August 2010
Completion Date
December 2011
Sponsors
Protgen Ltd
Source
Protgen Ltd
Record processing date
ClinicalTrials.gov processed this data on July 28, 2015
ClinicalTrials.gov page