Status:
UNKNOWN
Clinical Study of Liposomal Paclitaxel in Chinese Patients
Lead Sponsor:
Nanjing Sike Pharmaceutical Co., Ltd.
Conditions:
Solid Tumor
Eligibility:
All Genders
18-70 years
Phase:
PHASE1
Brief Summary
The purpose of this study is to determine the maximum tolerated dose and dose limiting toxicities of liposomal paclitaxel in Chinese patients with solid tumors in advanced stages.
Detailed Description
There are clinical trials show that paclitaxel is common option for the treatment of solid tumors. Liposomal paclitaxel has different pharmacokinetic features comparing with conventional paclitaxel. H...
Eligibility Criteria
Inclusion
- Age: from 18 to 70
- Patients with solid tuomors at advanced stage must be histologically or cytologically confirmed ,and be suitable for treating with Paclitaxel Liposome solo
- Eastern Cooperative Oncology Group (ECOG) performance status (PS)is from 0 to 2
- Patients who are expected to live at least 3 months
- Laboratory tests before the study: white blood count (WBC)≥4,000/mm³,absolute neutrophil count (ANC) ≥1,500/mm³, platelet count ≥100,000/mm³, hemoglobin≥9.0 g/dL, aspartate aminotransferase AST (sGOT) and alanine aminotransferase ALT(sGPT)≤2.5 times of normal value upper limit，serum creatinine≤1.0 time of normal value upper limit，total bilirubin≤1.5 times of normal value upper limit
- Not using chemotherapeutics (including test drug)before the study trial at least 4 weeks
- No obvious functional disturbance diseases of internal organs
- Complying with the study protocol
- Sign informed consent
- No Previous anaphylactic reaction to hormone
Exclusion
- Allergy to any medication or foods; History of hypersensitivity reactions to the conventional dosage form of paclitaxel or correlate excipients
- Active uncontrolled central nervous system metastasis
- Severe complications that obviously influence the compliance of patients
- Grade ≥1 neuropathy using NCI CTCAE version 3.0 criteria
- Taking other study medications or participating other clinical trial within 4w
- Having radiation therapy or operation within 4w
- Any non-remission toxicity ≥ CTC 1 in prior anticancer therapy(including radiation therapy) (except alopecie and hemoglobin)
- Pregnant or lactant women; fertile patients not using effective contraception during study
- No chief organ functional disturbance or diseases:
- abnormal liver and renal functions
- myocardial infarction
- active heart disease
- neuropathy or mental diseases including dementia or epilepsy
- blind、deaf、dumb or extremity disability
- known infection
- active diffuse intravascular coagulation
- Others whom researchers regard not eligible for the study.
Key Trial Info
Start Date :
April 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2009
Estimated Enrollment :
15 Patients enrolled
Trial Details
Trial ID
NCT00881101
Start Date
April 1 2009
End Date
December 1 2009
Last Update
April 15 2009
Active Locations (1)
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1
The ethics committee of Cancer Hospital of Fudan University
Shanghai, Shanghai Municipality, China, 200032