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Recently, Hengrui Pharmaceutical apatinib tablet new adaptive (chemical class 2.4) listing application (acceptance number: CXHS2000004) was approved by NMPA for the treatment of patients with advanced hepatocellular carcinoma who have failed or are insulable after receiving at least first-line systemic treatment.
this is the second adaptation approved by Apatini.
a Phase III clinical (NCT02329860) study for patients who have previously received at least one line of systemic treatment (solafinie and oxalipal) failure or inability to withstand advanced hepatocellular carcinoma Compared to the placebo group, the total survival of the apatinib group was significantly extended (8.7 vs. 6.8 months) and the risk of death was reduced in patients (HR:0.785, p=0.0476).
the Apatini group significantly extended the progression-free lifetime (4.5 vs. 1.9 months, HR:0.471, 0.0001) significantly increased the objective mitigation rate (10.7 percent vs. 1.5 percent).
safety, the most common ≥ incidence of adverse reactions above level 3 was hypertension (71 cases in the Apatini group (27.6%) vs placebo group 3 (2.3%)), hand-foot syndrome (46 (17.9%) vs 0), reduced platea count (34 (13.2%) vs 1 (0.8%)), reduced neutral granulocyte count (27 (10.5%)vs 0).
Methadone Apatini is a class 1 small molecule developed by Hengrui to target vascular endoderial cell growth factor recipient 2 (VEGFR-2) tyrosine kinase inhibitors, first approved by NMPA in 2014 for the treatment of patients with advanced gastric adenocarcinoma or gastroesophageal congenerative adenocarcinoma who have progressed or relapsed after at least 2 systematic chemotherapy.
In addition, apatinib monodone drugs or in combination with carelli pearl monoanti, fluorine parri, SHR-1210 or etoposide softgels to treat breast cancer, ovarian cancer, non-small cell lung cancer a variety of solid tumor adaptation has been in the clinical development stage.
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