Global Mitochondrial Myopathy Diagnosis & Treatment Market Forecasted to Observe an Enormous Growth By 2023

Mitochondrial myopathies are associated with mitochondrial diseases which are caused by certain nuclear DNA deletions and mutations. Mitochondrial myopathies affect mitochondria which is responsible for energy production within a cell associated with mitochondrial disease. Thus, they cause low energy and free radical production which results in a variety of symptoms.

The factors such as rising number of screening services for mitochondrial disorders, growing number of mitochondrial myopathy cases, increased government funding and incentives for rare genetic diseases are driving the market for mitochondrial myopathy diagnosis & treatment. However, poor treatment options and absence of curative treatment have constrained the market.

Considering all these factors, Mitochondrial Myopathy Diagnosis & Treatment Market is expected to reach $ 33.6 million by the end of 2020, this market is projected to growing at a CAGR of ~ 9.82 % during 2017-2020.

Key Findings:

Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like episodes (MELAS) and Progressive External Ophthalmoplegia (PEO) are the most commonly found conditions in patients with mitochondrial myopathy. The global MELAS diagnosis & treatment market is expected to grow at the CAGR of 19.39% during 2017 to 2020.
Genetic tests accounted for the largest market share in 2016, and is projected to grow at a CAGR of 10.11% during 2017 to 2020.
Supportive therapy captured the whole market share in 2016, and is projected to grow at a CAGR of 9.82% during 2017 to 2020.
Segments:

The Global Mitochondrial Myopathy Diagnosis & Treatment Market is segmented on the basis of type, diagnostic tests and therapy. Based on type, the market has been segmented as mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS), progressive external ophthalmoplegia (PEO), myoclonic epilepsy with ragged red fibres (MERRF), mitochondrial neurogastrointestinal encephalopathy syndrome (MNGIE), Kearns–Sayre syndrome (KSS), mitochondrial DNA depletion syndrome (MDS), Pearson syndrome, Leigh syndrome, neuropathy, ataxia, and retinitis pigmentosa (NARP). Based on the diagnostic tests, the market has been segmented as genetic tests, muscle biopsy and biochemical test. Based on the therapy, the market has been segmented as supportive therapy and targeted therapy.

Key players of Global Mitochondrial myopathy diagnosis & treatment Market:

Key players profiled in the report are Centogene AG, GeneDx, Ixchel Pharma, Khondrion BV, Mitobridge, NeuroVive Pharmaceutical AB, Reata Pharmaceuticals Inc., Stealth Biotherapeutics and others.

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Regional analysis:

The Americas account for the maximum market share due to favorable reimbursement scenario and greater expenditure on healthcare. The Americas mitochondrial myopathy diagnosis & treatment market is expected to reach USD 116.7 million by the end of 2025 at the CAGR of 19.39% during 2017 to 2025. The faster market uptake of new technology in the US is also an important driver of the market for global mitochondrial myopathy diagnosis & treatment. Europe is the second largest market due to large disposable income and rising awareness. Asia Pacific region is expected to have the most future potential and it is estimated to be led by China and India. The Asia Pacific mitochondrial myopathy diagnosis & treatment market is expected to reach USD 4.4 million by the end of 2020 at the CAGR of 9.94% during 2017 to 2020. The Middle East & Africa market is led by the gulf nations particularly Saudi Arabia and UAE. The regions of Africa are expected to witness a moderate growth due to poor economic and political conditions and poor healthcare penetration.

TABLE OF CONTENTS

1 INTRODUCTION

1.1 Definition

1.2 Scope of Study

1.3 Research Objective

1.4 Assumptions & Limitations

1.4.1 Assumptions

1.4.2 Limitations

1.5 Market Structure

2 RESEARCH METHODOLOGY

2.1 Research Process

2.2 Primary Research

2.3 Secondary Research

3 MARKET DYNAMICS

3.1 Introduction

3.2 Drivers

3.2.1 Rise In Number Of Mitochondrial Myopathy Incidence Rate And Growing Number Of Screening ervices.

3.2.2 Government Funding And Incentives For Rare Genetic Diseases

3.3 Restraints

3.3.1 Poor Treatment Options And Absence Of Curative Treatment

3.3.2 Lack Of Awareness And Diagnosis Of The Rare Mitochondrial Disorders

3.4 Opportunities

3.4.1 Faster Market Uptake And Low Marketing Cost

3.4.2 Research And Development

3.5 Challenges

4 MARKET FACTOR ANALYSIS

4.1 Porter’s Five Forces Analysis

4.1.1 Threat From A New Entrant

4.1.2 Bargaining Power Of Buyer

4.1.3 Bargaining Power Of Supplier

4.1.4 Threat From Substitute

4.1.5 Intensity Of Competitive Rivalry

4.2 Pipeline Analysis

4.2.1 Introduction

4.2.2 KH176

4.2.3 Elamipretide

4.2.4 RTA 408

4.2.5 IXC 103

4.2.6 NV556

4.3 Mega Trends

… Toc Continued

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