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Type 2 Diabetes Mellitus Therapeutics in South-East Asia Markets to 2023-Increasing Usage of Newer Therapies and Expanding Treatment Population to Encourage Robust Growth

 



(PharmaNewsWire.Com, October 26, 2017 ) Diabetes mellitus is a group of metabolic diseases characterized by chronic hyperglycemia-high blood glucose levels-that results from defects in insulin secretion, insulin action, or a combination of these. Chronic hyperglycemia is associated with the long-term damage, dysfunction and failure of multiple organs including the eyes, kidneys, nerves, heart and blood vessels. Prevalence of the disease has risen rapidly in recent decades in the assessed South-East Asia countries, primarily as a result of rising obesity, a major risk factor for type 2 diabetes mellitus (T2DM). This has resulted in a large and competitive market landscape, with a number of drugs vying for various market segments across multiple lines of therapy.

For more information about this report: http://www.reportsweb.com/type-2-diabetes-mellitus-therapeutics-in-south-east-asia-markets-to-2023

T2DM treatment has been revolutionized in the past decade, especially with the increased use of new therapies. The marketed products landscape comprises a wide range of treatment options, including biguanide (metformin), sulfonylureas, thiazolidinediones, GLP-1 receptor agonist, DPP-4 inhibitor, SGLT-2 inhibitor, and insulin therapies. Nevertheless, significant unmet need remains for products that can offer better glycemic control, as well as the prevention and cure of diabetic complications, such as diabetic nephropathy, retinopathy, and cardiovascular disease.

Scope
The current T2DM market in South-East Asia contains novel products, including Jardiance, a SGLT-2 inhibitor; Victoza, a GLP-1 receptor agonist; and Januvia, a DPP-4 inhibitor.
-What are the competitive advantages of the existing novel drugs?
There are over 609 active pipeline molecules, with most of the late-stage investigational drug candidates featuring improved dosing regimens and administration routes compared with currently marketed products and combination therapies.
-Which classes of novel drugs are most prominent in the pipeline?
-Is there potential for pipeline molecules to address unmet needs within the T2DM market?
Analysis of clinical trials since 2006 identified that the failure rates of T2DM molecules were highest in Phase III, at 62.1%, with the overall attrition rate for T2DM standing at 88.3%.
-How do failure rates vary by product stage of development, molecule type, and mechanism of action?
-How do other factors, such as average trial duration and trial size, influence the costs and risks associated with product development?
Over the 2016-2023 forecast period, the T2DM therapeutics market in South-East Asia is expected to increase in value at a CAGR of 6.3%, from $1.92 billion to over $2.96 billion.
-Which markets make the most significant contribution to the regional market size?
-What are the epidemiology trends in these markets?
-Will new market entrants lead to substantial changes in annual therapy costs?
-How will different treatment usage patterns impact growth in the eight assessed South-East Asia markets?
Rising T2DM prevalence and the uptake of newer therapies will lead to significant market growth over the forecast period, despite generic sales erosion resulting from patent expirations.
-Will patent expirations or emerging pipeline molecules threaten the commercial success of existing drugs?

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Reasons to buy
-Understand the clinical context of T2DM by considering symptoms, etiology, pathophysiology, epidemiology, diagnosis, and treatment options.
-Identify the therapeutic strategies, products, and companies that dominate the current marketed product landscape and recognize gaps and areas of unmet need.
-Identify key pipeline trends in molecule type, administration route, mechanism of action, and novelty.
-Consider market opportunities and potential risks by examining trends in T2DM clinical trial size, duration, and failure rate by stage of development, molecule type, and mechanism of action.
-Recognize the late-stage pipeline molecules that have demonstrated strong therapeutic potential in T2DM by examining clinical trial data and multi-scenario product forecast projections.
-Compare treatment usage patterns, annual therapy costs, and market growth projections for South Korea, Singapore, Taiwan, Malaysia, the Philippines, Thailand, Vietnam, and Indonesia.
-Discover trends in licensing and co-development deals concerning T2DM products, and identify the major strategic consolidations that have shaped the commercial landscape.


Table of Contents
1 Table of Contents 4
1.1 List of Tables 7
1.2 List of Figures 7
2 Introduction 10
2.1 Disease Introduction 10
2.2 Epidemiology 11
2.3 Symptoms 11
2.4 Etiology and Pathophysiology 12
2.5 Diagnosis 14
2.6 Classification 16
2.7 Prognosis 17
2.8 Treatment Options 17
2.8.1 Treatment Algorithm 18
2.8.2 Non-insulin T2DM Therapies 20
2.8.3 Insulin T2DM Therapies 23
2.9 Treatment Segments 25
2.9.1 Non-Insulin Therapies 25
2.9.2 Insulin Therapies 41
2.10 Co-morbidities and Complications 44
2.11 Non-pharmacological Treatments 46
2.11.1 Dietary Interventions 46
2.11.2 Exercise 46
3 Marketed Products 47
3.1 Overview 47
3.2 Biguanides 48
3.2.1 Metformin 48
3.3 Sulfonylureas 49
3.4 Thiazolidinediones 51
3.4.1 Pioglitazone 51
3.4.2 Duvie (lobeglitazone)-Chong Kun Dang 52
3.5 GLP-1 Receptor Agonists 52
3.5.1 Byetta (exenatide)-AstraZeneca 52
3.5.2 Bydureon (exenatide)-AstraZeneca 53
3.5.3 Victoza (liraglutide)-Novo Nordisk 55
3.5.4 Lyxumia (lixisenatide)-Sanofi 56
3.5.5 Tanzeum (albiglutide)-GlaxoSmithKline 58
3.5.6 Trulicity (dulaglutide)-Eli Lilly 59
3.6 DPP-4 Inhibitors 60
3.6.1 Januvia (sitagliptin)-Merck & Co. 60
3.6.2 Galvus (vildagliptin)-Novartis 62
3.6.3 Onglyza (saxagliptin)-Bristol-Myers Squibb/AstraZeneca 63
3.6.4 Tradjenta (linagliptin)-Bristol-Myers Squibb/AstraZeneca 64
3.6.5 Zemiglo (gemigliptin)-LG Life Sciences 65
3.6.6 Suganon (evogliptin)-Dong-A ST 66
3.6.7 Gadret (anagliptin)-JW Pharmaceutical 67
3.6.8 Nesina (alogliptin)-Takeda 67
3.6.9 Tenelia (teneligliptin)-Mitsubishi Tanabe Pharma 68
3.7 SGLT-2 Inhibitors 69
3.7.1 Forxiga (dapagliflozin)-AstraZeneca 69
3.7.2 Invokana (canagliflozin)-Janssen 71
3.7.3 Jardiance (empagliflozin)-Boehringer Ingelheim 72
3.7.4 Suglat (ipragliflozin)-Astellas 73
3.8 Insulin Therapies 74
3.8.1 Lantus (insulin glargine)-Sanofi 74
3.8.2 Levemir (insulin detemir)-Novo Nordisk 75
3.8.3 Tresiba (insulin degludec)-Novo Nordisk 76
3.8.4 Toujeo (insulin glargine)-Sanofi 77
3.9 Comparative Efficacy and Safety of Marketed Products 78
4 Pipeline Analysis 84
4.1 Overview 84
4.2 Pipeline by Stage of Development, Molecule Type, Route of Administration and Program Type 85
4.3 Pipeline by Molecular Target 87
4.4 Promising Pipeline Molecules 91
4.4.1 NN-9535 (subcutaneous semaglutide) and OG-217SC (oral semaglutide)-Novo Nordisk 91
4.4.2 Ertugliflozin-Pfizer 95
4.4.3 Bexagliflozin-Theracos 96
4.4.4 Omarigliptin-Merck & Co. 97
4.4.5 Sotagliflozin-Sanofi 99
4.5 Comparative Efficacy and Safety of Pipeline Products 101
4.6 Product Competitive Framework 102

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ReportsWeb.com

Rajat Sahni

+1-646-491-9876

sales@reportsweb.com

Source: EmailWire.Com

Source: EmailWire.com


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