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*For medical professionals only
Insulin glargine rissinatide compound preparation is a combination of insulin glargine (basal insulin analogue) and risnatide (GLP-1RA*), which effectively helps patients achieve comprehensive blood glucose goals once a day, and the risk of hypoglycemia is small, and there is no weight
gain 。 Its two-component mechanism is complementary, multi-target regulation, and synergistic inhibition of the pathogenesis of sevenfold diabetes.
Targeted direct attack, synergistic improvement of two core physiological defects, while protecting the patient's islet β cells while effectively improving insulin resistance
.
It is worth mentioning that the advantageous ratio of insulin glargine and risnatide (1IU:1ug and 2IU:1ug) is tailored for Chinese diabetic patients, helping to achieve a good initial treatment experience and full-course management, which will open a new era
of "high-quality compliance".
。 Inadequate initiation of treatment and low patient compliance are the main reasons for unsatisfactory glycemic management, among which concerns about the occurrence of hypoglycemia and weight gain are the main concerns of patients initiating and adhering to insulin therapy [3-4].
Therefore, treatment regimens that can achieve strong hypoglycemic reduction, safe onset and worry-free weight will better meet the treatment needs
of Chinese patients with high quality standards.
* Glucagon-like peptide-1 receptor agonist
Diabetes research and clinical practice 183 (2022): 109119.
[2] Wang, Limin, et al.
"Prevalence and treatment of diabetes in China, 2013-2018.
" JAMA 326.
24 (2021): 2498-2506.
[3] Kim SG, et al.
J Diabetes Investig 2017,8(3):346-353[4] Berard L, et al.
Diabetes Obes Metab 2018,20(2):301-308 [5] Standards of Medical Care in Diabetes.
Diabetes Care 2022, 131-140[6] CDS.
Chinese Guidelines for the Prevention and Treatment of Type 2 Diabetes.
2020 Edition[7] Yang W, et al.
Diabetes Obes Metab 2022,24(8):1522-1533 [8] Rosenstock J.
, et al.
“Advancing therapy in suboptimally controlled basal insulin-treated type 2 diabetes: Clinical outcomes with iGlarLixi versus premix BIAsp 30 in the SoliMix randomized controlled trial.
” Diabetes Care 2021 Jun; dc210393.
The web version of the doctor's website is online, please scan the QR code below or click to read the original article
,
you can browse more endocrinology frontier information without downloading
within the meaning of the Private Securities Litigation Reform Act of 1995, as amended.
Forward-looking statements are not statements
of historical fact.
These statements include forecasts and estimates of the marketing and other potential of the product, or forecasts and estimates
of the potential future revenue of the product.
Words such as "expects," "anticipates," "believes," "intends," "estimates," "plans" and similar expressions may generally be used to base the determination of forward-looking statements
.
Although Sanofi's management believes that the expectations reflected in such forward-looking statements are reasonable, investors are cautioned that these forward-looking information and statements are subject to a number of risks and uncertainties, many of which are difficult to predict and generally outside Sanofi's control, which could cause actual results and developments to differ
materially from those expressed, implied or predicted in the forward-looking information and statements 。 These risks and uncertainties include, inter alia, decisions or delays by regulatory authorities or decisions of relevant agencies on matters that may affect the availability or commercial potential of the product candidate, the likelihood that an approved product candidate will not be commercially successful, including uncertainties inherent in research and development, future clinical data and analysis, including data obtained and analyzed after the product is marketed, unexpected safety, quality or manufacturing issues, general competition, The risks associated with future litigation related to intellectual property rights and the eventual outcome of such litigation, as well as volatile economic and market conditions, including the impact of the pandemic on the financial position of us, our customers, suppliers and other business partners, and any party, as well as on our employees and the global economy
.
The significant impact of the pandemic on any of these may also have a negative impact
on us.
This is changing rapidly, with additional impacts that we don't currently know about, and exacerbating other risks
previously identified.
These risks and uncertainties also include those discussed or clarified by Sanofi in its public filings with the U.
S.
Securities and Exchange Commission (SEC) and the French Authority for the Financial Markets (AMF), including "Risk Factors" and "Forward-Looking Statement Warnings"
set forth in Sanofi's Annual Report on Form 20-F for the year ended December 31, 2020.
Except where applicable law exists, Sanofi undertakes no obligation
to update and revise any forward-looking information and statements.
4M Number: MAT-CN-2300608 Plan Effective Date: January
2023 This number is only used as Sanofi's confirmation of the authenticity of scientific and clinical data sources in the therapeutic field of Sanofi-related drugs mentioned in this article.
does not serve as a confirmation or guarantee by Sanofi of the accuracy, timeliness and completeness of all contents of this article;
This article is intended for use by healthcare professionals for academic communication or medical information purposes only and does not constitute a recommendation or promotion
of any drug or treatment regimen.
The information contained in this article should not be a substitute for medical advice
provided by a healthcare professional.
Shanghai, China, January 12, 2023 – Sanofi China announced that the National Medical Products Administration (NMPA) of China has approved the marketing application for insulin glargine risnatide injections (I), (II), which are suitable for adults with type 2 diabetes mellitus (T2DM) with poor glycemic control In combination with other oral hypoglycemic drugs on the basis of diet and exercise, it is also the first innovative product
approved by Sanofi China this year.
Insulin glargine rissinatide compound preparation is a combination of insulin glargine (basal insulin analogue) and risnatide (GLP-1RA*), which effectively helps patients achieve comprehensive blood glucose goals once a day, and the risk of hypoglycemia is small, and there is no weight
gain 。 Its two-component mechanism is complementary, multi-target regulation, and synergistic inhibition of the pathogenesis of sevenfold diabetes.
Targeted direct attack, synergistic improvement of two core physiological defects, while protecting the patient's islet β cells while effectively improving insulin resistance
.
It is worth mentioning that the advantageous ratio of insulin glargine and risnatide (1IU:1ug and 2IU:1ug) is tailored for Chinese diabetic patients, helping to achieve a good initial treatment experience and full-course management, which will open a new era
of "high-quality compliance".
Mr.
Shi Wang, President of Sanofi Greater China: "Benefiting from the government's positive measures to accelerate the approval of a number of innovative drugs, Sanofi has continued to introduce global innovative therapies to the Chinese market
for more than 40 years after entering China.
In the field of diabetes, we have been exploring more suitable diagnosis and treatment solutions
for Chinese patients with more than 100 years of accumulation.
From the tens of millions of Chinese doctors and patients trusted by insulin glargine U100 and insulin glargine U300 to today's insulin glargine risnatide injection, we are committed to improving drug access with continuous innovation to help more Chinese diabetics rejuvenate their lives and have 'high-quality standards, high-quality life'
.
" ”
。 Inadequate initiation of treatment and low patient compliance are the main reasons for unsatisfactory glycemic management, among which concerns about the occurrence of hypoglycemia and weight gain are the main concerns of patients initiating and adhering to insulin therapy [3-4].
Therefore, treatment regimens that can achieve strong hypoglycemic reduction, safe onset and worry-free weight will better meet the treatment needs
of Chinese patients with high quality standards.
Professor Yang Wenying of China-Japan Friendship Hospital, the principal investigator of Lixilan-O-AP in the phase III clinical trial of insulin glargine risnatide injection in China, said: "Quality compliance is the general trend
of diabetes management.
Patients need to achieve short-term goals of glycaemic management and further reduce the incidence of long-term complications, so as to truly improve
their quality of life.
We are pleased to see that many clinical trials around the world have proved that the compound preparation represented by the combination preparation of insulin glargine risnatide as an ideal treatment plan with complementary mechanism, synergy and vice reduction, can better improve the blood sugar
of patients.
”
As the principal investigator of another phase III clinical trial of Lixilan-L-CN of insulin glargine risnatide injection, Professor Guo Xiaohui of Peking University First Hospital said: "Two studies of insulin glargine risnatide combination preparation LixiLan-O AP and LixiLan-L CN also proved that it has more obvious clinical advantages in the Chinese group, providing more effective, safe and convenient treatment options
for Chinese patients.
The approval of insulin glargine risnatide injection in China is very exciting, and it will undoubtedly open a new journey
of 'high-quality standards' for diabetes treatment in China.
" ”
//
- Powerful sugar control: According to the LixiLan-O-AP study, glycated hemoglobin in insulin glargine rissinatide compound preparation can be reduced by up to 1.
9%, and about 80% of patients achieve blood glucose standards
.
At the same time, taking into account fasting and postprandial blood glucose, patients control blood glucose levels smoothly throughout the day to achieve more effective blood glucose management [7];
- Safe start: According to the SoliMix study, compared with premixed insulin, insulin glargine risnatide combination preparation can reduce the incidence of hypoglycemia by 68%; Several studies have shown a very low rate of severe hypoglycaemic events, resulting in a more reassuring treatment experience [8];
- Weight worry-free: According to SoliMix research, compared with premixed insulin, insulin glargine rissinatide compound preparation has obvious weight benefits, and the proportion of patients who meet the safety standard without weight gain increases to nearly 3 times, effectively improving the quality of life and achieving all-round comprehensive benefits [8].
* Glucagon-like peptide-1 receptor agonist
References:
[1] Sun, Hong, et al.Diabetes research and clinical practice 183 (2022): 109119.
[2] Wang, Limin, et al.
"Prevalence and treatment of diabetes in China, 2013-2018.
" JAMA 326.
24 (2021): 2498-2506.
[3] Kim SG, et al.
J Diabetes Investig 2017,8(3):346-353[4] Berard L, et al.
Diabetes Obes Metab 2018,20(2):301-308 [5] Standards of Medical Care in Diabetes.
Diabetes Care 2022, 131-140[6] CDS.
Chinese Guidelines for the Prevention and Treatment of Type 2 Diabetes.
2020 Edition[7] Yang W, et al.
Diabetes Obes Metab 2022,24(8):1522-1533 [8] Rosenstock J.
, et al.
“Advancing therapy in suboptimally controlled basal insulin-treated type 2 diabetes: Clinical outcomes with iGlarLixi versus premix BIAsp 30 in the SoliMix randomized controlled trial.
” Diabetes Care 2021 Jun; dc210393.
The web version of the doctor's website is online, please scan the QR code below or click to read the original article
,
you can browse more endocrinology frontier information without downloading
Sanofi forward-looking statements
within the meaning of the Private Securities Litigation Reform Act of 1995, as amended.
Forward-looking statements are not statements
of historical fact.
These statements include forecasts and estimates of the marketing and other potential of the product, or forecasts and estimates
of the potential future revenue of the product.
Words such as "expects," "anticipates," "believes," "intends," "estimates," "plans" and similar expressions may generally be used to base the determination of forward-looking statements
.
Although Sanofi's management believes that the expectations reflected in such forward-looking statements are reasonable, investors are cautioned that these forward-looking information and statements are subject to a number of risks and uncertainties, many of which are difficult to predict and generally outside Sanofi's control, which could cause actual results and developments to differ
materially from those expressed, implied or predicted in the forward-looking information and statements 。 These risks and uncertainties include, inter alia, decisions or delays by regulatory authorities or decisions of relevant agencies on matters that may affect the availability or commercial potential of the product candidate, the likelihood that an approved product candidate will not be commercially successful, including uncertainties inherent in research and development, future clinical data and analysis, including data obtained and analyzed after the product is marketed, unexpected safety, quality or manufacturing issues, general competition, The risks associated with future litigation related to intellectual property rights and the eventual outcome of such litigation, as well as volatile economic and market conditions, including the impact of the pandemic on the financial position of us, our customers, suppliers and other business partners, and any party, as well as on our employees and the global economy
.
The significant impact of the pandemic on any of these may also have a negative impact
on us.
This is changing rapidly, with additional impacts that we don't currently know about, and exacerbating other risks
previously identified.
These risks and uncertainties also include those discussed or clarified by Sanofi in its public filings with the U.
S.
Securities and Exchange Commission (SEC) and the French Authority for the Financial Markets (AMF), including "Risk Factors" and "Forward-Looking Statement Warnings"
set forth in Sanofi's Annual Report on Form 20-F for the year ended December 31, 2020.
Except where applicable law exists, Sanofi undertakes no obligation
to update and revise any forward-looking information and statements.
4M Number: MAT-CN-2300608 Plan Effective Date: January
2023 This number is only used as Sanofi's confirmation of the authenticity of scientific and clinical data sources in the therapeutic field of Sanofi-related drugs mentioned in this article.
does not serve as a confirmation or guarantee by Sanofi of the accuracy, timeliness and completeness of all contents of this article;
This article is intended for use by healthcare professionals for academic communication or medical information purposes only and does not constitute a recommendation or promotion
of any drug or treatment regimen.
The information contained in this article should not be a substitute for medical advice
provided by a healthcare professional.