Malignant Ascites
Conditions
Interventions
Group SCB-313:Intraperitoneal injection, once a day, 10mg each time (reconstituted with 500ml 0.9% sodium chloride), 1 week after single dose, continuous dose 3 times total for 1 treatment cycle
Sponsors
Shanghai East Hospital
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Histologically or cytologically confirmed as malignant solid tumor. 2. Malignant ascites requiring puncture drainage evaluated by investigators, defined as: 1) if tumor cells are detectable in the ascites, 2) if previous surgical operation reveals extensive abdominal cavity metastasis, 3) if there is image evidence of extensive metastasis in the abdominal cavity, 4) if it is determined by ascites routine and ascites biochemical examination as exudate; 3. Eastern Cooperative Oncology Group (ECOG) performance status: 0 to 3. 4. Life expectancy of at least 12 weeks. 5. Aged >= 18 years. 6. Body weight >= 45 kg and body mass index (BMI) >17 kg/m2 7. Adequate hematological function, defined as: 1) Platelet count >=100*10^9/L, 2) Prothrombin time and activated partial thromboplastin time = 1.5*10^9/L, and (d) Hemoglobin >= 9 g/dL. 8. Adequate renal function, defined as serum creatinine 50 mL/minute. 9. Adequate liver function, defined as: 1) Aspartate aminotransferase and alanine aminotransferase = 2.8 g / dL (patient can use albumin to meet the standard) 11. If the serum pregnancy test of a female patient with fertility is negative within 7 days prior to the initial administration, and she is willing to use effective birth control/contraception method for contraception within 6 months after discontinuation of SCB-313.( Female patients with fertility exclude women who have undergone sterilization or menopause, which is defined as a menstrual period that lasts for one year or more without any other medical reason.) All male and female patients with reproductive potential must agree to take effective contraceptive measures during the study period and within 6 months after discontinuation of SCB-313. Note: Contraceptive methods considered to be effective include: complete abstinence, intrauterine devices, double barrier contraceptive methods (such as condom plus spermicide diaphragm), implanted contraceptives, hormonal contraceptives (contraceptives, implants agent, transdermal patch, hormonal vaginal device or injection for extended release), or the partner has removed the vas deferens and confirmed that it is azoospermia 12. Willing to attend follow-up visits according to study protocol.
Exclusion criteria
Exclusion criteria: 1. Loculated ascites not amenable to full drainage or benefit from abdominal treatment 2. Acute or chronic infection (such as tuberculosis) requiring antiviral or intravenous antibiotics within 2 weeks prior to enrollment. 3. Untreated central nervous system metastatic disease, leptomeningeal disease, or cord compression. 4. Residual adverse events (AEs) 480 msec at baseline. 7. Uncontrolled hypertension defined as systolic blood pressure >= 140 mmHg and/or diastolic blood pressure >= 90 mmHg confirmed upon repeated measures. 8. Left ventricular ejection fraction < 50% as determined by echocardiography performed at screening 9. Hormone therapy or palliative extra abdominal radiotherapy within 1 week, prior anti-tumor therapy (chemotherapy) within 2 weeks, or other test drug within 4 weeks prior to enrollment. 10. Major surgery within 4 weeks prior to enrollment. 11. Patient with ileus within 30 days prior to screening. 12. Known portal vein obstruction (due to either prehepatic, hepatic, or posthepatic condition) which per Investigators judgement, is the primary or significant cause of ascites. 13. Positive serology test for human immunodeficiency virus type 1 and 2, or known history of other immunodeficiency disease. 14. Uncontrolled active hepatitis. 15. Scheduled participation in another clinical study involving an investigational product or device during the course of this study. 16. Previous treatment with a TRAIL-based therapy or Death Receptor (DR) 4/5 agonist therapy. 17. Known or suspected hypersensitivity to any component of the SCB 313. 18. Any further condition which, according to the investigator, may result in undue risk of the patient by participating in the present study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| MTD for single and multiple doses of SCB-313 in the abdominal cavity;Dose-limiting toxicity (DLT);The severity of the adverse events associated with SCB-313 treatment, the incidence of serious adverse events (SAE), and the severity and incidence of adverse events (TEAE) during the DLT-observation period developed in patients, and the classification is based on the National Cancer Institute General Adverse Even; | — |
Countries
China
Contacts
Public ContactJin Li
Shanghai East Hospital
Outcome results
None listed