Malignant Ascites is a common complication of malignant tumor. The objective of this study is to evaluate the safety, efficacy, and pharmacokinetic characteristics of intraperitoneal perfusion with Docetaxel Polymeric Micelles (SIM0388) for injection in patients with malignant ascites
The study starts with a dose escalation part followed by a dose expansion part. The primary objective of the dose escalation part is to evaluate the safety and tolerability of SIM0388 peritoneal perfusion, and determine the Maximum tolerated dose (MTD) and/or the recommended dose(s) (RD) of SIM0388 peritoneal perfusion. The primary objective of the dose expansion part is to evaluate the efficacy of SIM0388 intraperitoneal perfusion in the treatment of malignant ascites.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
50
Shanghai Gobroad Cancer Hospital
Shanghai, Shanghai Municipality, China
RECRUITINGDose escalation:Dose limited toxicity (DLT)
Dose-limiting toxicity(DLT)
Time frame: DLT observation period (up to 35 days)
Dose escalation phase: Adverse Events (AEs) and Serious Adverse Events (SAEs)
Adverse events will be assessed by investigator(s) according to NCI-CTCAE v5.0.
Time frame: Through study completion, an average of 2 years
Dose expansion phase:ORRa(Objective response rate in ascites)
Ascites ORRa assessed according to WHO criteria
Time frame: Through study completion, an average of 2 years
Dose expansion phase:TTPa (Time to progress in ascites)
Ascites TTPa assessed according to WHO criteria
Time frame: Through study completion, an average of 2 years
Dose expansion phase:PuFS (Puncture/drainage -free survival)
PuFS
Time frame: Through study completion, an average of 2 years
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.