Efficacy and Safety of Apatinib Combined With TACE in Patients With Hepatocellular Carcinoma
- Sponsor
- Shanghai Zhongshan Hospital
- Study ID
- NCT03510416
- Phase
- PHASE2
- Status
- Unknown
Conditions
- Hepatocellular Carcinoma Refractory to Transcatheter Arterial Chemoembolization
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- Apatinib — DRUGapatinib is a kind of Inhibitor of VEGFR-2
- TACE — RADIATIONEpirubicin,ultra-fluid lipiodol and gelatin sponge articles are used in TACE.
Study Details
Efficacy and Safety of Apatinib Combined With TACE in Patients With Hepatocellular Carcinoma Refractory to Transcatheter Arterial Chemoembolization .
Key Dates
- Start date
- May 1, 2018
- Status verified
- Apr 2018
- Primary completion
- Jun 30, 2019
- Completion
- Dec 31, 2019
Study Design
- Enrollment
- 22 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: apatinib combined with TACEApatinib is administered after TACE 4-7 days, and TACE treatment is performed after discontinuation of apatinib for 4 days.Every 28 days is a cycle.
Primary Outcome Measure
Time To Progression [ Time Frame: From the date of first procedure of apatinib combined with TACE until the time when the disease progresses, assessed up to 14 months ]
Central Contacts
- zhiping Yan, MD13681971205
- wei Zhang, MD13917737593