Overview

Evaluating the Safety and Efficacy of SB Injection in Patients With Advanced or Metastatic Gastric Cancer

Status:
Unknown status
Trial end date:
1969-12-31
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to determine efficacy of SB injection in Gastric Cancer.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
SBPharmaceutical IND, Co., LTD
Criteria
Inclusion Criteria:

- Age of 18years or over

- Patients who had failed more than 1 cycle of standard therapy with advanced or
metasatic stage and with measurable lesions

- Life expectancy >/= 5 months

- Not available to any of resectable surgery or radiotherapy

- Patients with adequate organ(e.g. heart, kidney, liver)and bone marrow function, as
defined by

1. Absolute neutrophil count(ANC)>/= 1.0 x 10^9/L, Platelet count >/= 75 x 10^9/L

2. Total bilirubin < 2.0mg/dL

3. Aspartate Aminotransferase(AST) and/or Alanine Aminotransferase(ALT) < 5 x Upper
Limit Normal(ULN)

4. creatinine < 2 x ULN

- ECOG status 0 to 2

- Female volunteers admitted to the study must be using a reliable means of
contraception and must have a negative blood or urine pregnancy test at least 7days
ago

- Patients or their legal representatives who have signed the informed consent form.

Exclusion Criteria:

- Known brain or spinal cord metastases

- Patients who have received chemotherapy within the previous 4 weeks

- Patients who have received radiotherapy related tp Gastric cancer within 4weeks

- Patients who have participated in other clinical study within the previous 4weeks

- Pregnancy (absence to be confirmed by ß-hCG test) or lactation period

- Human immunodeficiency virus(HIV) antibody (+)

- Have active infection or serious concomitant systemic disorder incompatible with the
study

- Clinically hypertension or diabete mellitus not well controlled with medication

- Clinically significant cardiac disease(e.g. congestive heart failure, symptomatic
coronary artery disease and cardiac arrhythmias) or myocardial infarction

- Presence or history of malignancy other than Gastirc cancer within 5years

- Have severe Neurologic or psychological disorder

- Patients who have history of allery with this investigational drug(SB injection)

- Obvious cognitive or physical impairment that would prevent participation