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Shanghai, September 28, 2021/PRNewswire/ - Sanofi China announced that the National Medical Products Administration (NMPA) has formally accepted the company's fixed-proportion combination of basal insulin and GLP-1RA *SOLIQUA® (iGlarLixi) New drug listing application
iGlarLixi is an injectable hypoglycemic drug, which is composed of insulin glargine 100U/mL and risnatide in a fixed ratio
Experts in the diabetes field are confident that this innovative drug will bring benefits to Chinese diabetic patients
Professor Guo Xiaohui, the main investigator of the LixiLan-L CN Phase III clinical trial in China, from the Department of Endocrinology, Peking University First Hospital, said: “China has approximately 129.
Dr.
The results of the global phase III clinical study of iGlarLixi show that in patients who have received oral hypoglycemic drugs, basal insulin or GLP-1 receptor agonists (daily or weekly preparations) but still have poor blood glucose levels, it may be compared with basal insulin or Compared with GLP-1 receptor agonists alone, iGlarLixi has a better effect on reducing the level of glycosylated hemoglobin (HbA1c), and the proportion of patients reaching the standard is higher (HbA1c <7%)
The results of the study also showed that compared with basal insulin, iGlarLixi does not increase the risk of hypoglycemia and weight gain; compared with GLP-1 receptor agonists, iGlarLixi causes fewer gastrointestinal reactions due to the stepwise titration of doses
In June of this year, Sanofi announced the results of SoliMix, the first head-to-head study comparing iGlarLixi and premixed insulin at the annual meeting of the American Diabetes Association (ADA)
* Soliqua® (iGlarLixi) has not yet been approved in China
[1] Yongze Li, Di Teng, Xiaoguang Shi, et al.
[2] Aroda, Vanita R.
[3] Rosenstock, Julio, et al.
[4] Blonde L, et al.
[5] Rosenstock, Julio et al.
About Sanofi China
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Source: Sanofi China