ライソゾーム貯蔵病治療薬市場- 世界の産業規模、シェア、動向、機会、予測、治療別、適応症別、エンドユーザー別、地域別セグメント、競合、2020年～2030年

世界のライソゾーム貯蔵病治療薬市場は2024年に76億米ドルと評価され、2030年までのCAGRは7.20%で、予測期間中に目覚ましい成長を遂げると予測されています。

ライソゾーム貯蔵疾患（LSD）は、ライソゾーム貯蔵障害としても知られ、ライソゾームの異常を特徴とする稀な遺伝性疾患群です。リソソームは様々な分子や細胞の老廃物を分解する細胞小器官です。遺伝子変異によりリソソームが機能不全に陥ると、正常な機能を効果的に発揮できなくなります。その結果、未消化の物質がリソソーム内に蓄積し、細胞のプロセスを混乱させます。この蓄積は様々な症状や臓器障害を引き起こし、体内の複数のシステムに影響を及ぼします。ほとんどのLSDは、特定のリソソーム酵素の欠乏に起因します。これらの酵素は、脂質（脂肪）、糖タンパク質、ムコ多糖類などの複雑な分子を分解する役割を担っています。特定の酵素が欠乏または欠損すると、対応する基質がリソソーム内に蓄積します。LSDは50種類以上あり、それぞれが特定のリソソーム酵素欠損に関連しています。LSDの例としては、ゴーシェ病、テイ-サックス病、ファブリー病、ポンペ病、ニーマン-ピック病、ムコ多糖症（MPS）などがあります。それぞれのLSDには独特の臨床的特徴と病気の経過があります。例えば、米国国立衛生研究所（NIH）によると、2022年4月現在、ポンペ病は米国で約4万人に1人が罹患しています。

市場促進要因

研究開発の進展

主な市場課題

疾病メカニズムに対する理解の遅れ

主要市場動向

シャペロン療法

目次

第1章 概要

第2章 調査手法

第3章 エグゼクティブサマリー

第4章 顧客の声

第5章 世界のライソゾーム貯蔵病治療薬市場展望

• 市場規模・予測
  • 金額別
• 市場シェア・予測
  • 治療（酵素補充療法、幹細胞療法、基質還元療法、その他）
  • 適応症別（ゴーシェ病、ファブリー病、ポンペ病、ムコ多糖症、その他）
  • エンドユーザー（病院、診療所）別
  • 地域別
  • 企業別（2024）
• 市場マップ

第6章 アジア太平洋地域のライソゾーム貯蔵病治療薬市場展望

• 市場規模・予測
• 市場シェア・予測
• アジア太平洋地域：国別分析
  • 中国
  • インド
  • オーストラリア
  • 日本
  • 韓国

第7章 欧州のライソゾーム貯蔵病治療薬市場展望

• 市場規模・予測
• 市場シェア・予測
• 欧州：国別分析
  • フランス
  • ドイツ
  • スペイン
  • イタリア
  • 英国

第8章 北米のライソゾーム貯蔵病治療薬市場展望

• 市場規模・予測
• 市場シェア・予測
• 北米：国別分析
  • 米国
  • メキシコ
  • カナダ

第9章 南米のライソゾーム貯蔵病治療薬市場展望

• 市場規模・予測
• 市場シェア・予測
• 南米：国別分析
  • ブラジル
  • アルゼンチン
  • コロンビア

第10章 中東・アフリカのライソゾーム貯蔵病治療薬市場展望

• 市場規模・予測
• 市場シェア・予測
• 中東・アフリカ：国別分析
  • 南アフリカ
  • サウジアラビア
  • アラブ首長国連邦

第11章 市場力学

• 促進要因
• 課題

第12章 市場動向と発展

• 最近の動向
• 製品上市
• 合併と買収

第13章 世界のライソゾーム貯蔵病治療薬市場：SWOT分析

第14章 ポーターのファイブフォース分析

• 業界内の競合
• 新規参入の可能性
• サプライヤーの力
• 顧客の力
• 代替品の脅威

第15章 PESTEL分析

第16章 競合情勢

• Pfizer, Inc.
• Sanofi SA
• BioMarin Pharmaceutical Inc
• Actelion Ltd.
• Raptor Pharmaceutical Corp.
• Protalix Biotherapeutics Inc.
• Amicus Therapeutics, Inc.
• Quest Diagnostics Inc.
• Amicus Therapeutics Inc.
• Shire Plc

第17章 戦略的提言

第18章 調査会社について・免責事項

Global Lysosomal Storage Diseases Therapeutics Market was valued at USD 7.60 billion in 2024 and is anticipated to witness an impressive growth in the forecast period with a CAGR of 7.20% through 2030. Lysosomal Storage Diseases (LSDs), also known as lysosomal storage disorders, are a group of rare genetic disorders characterized by abnormalities in lysosomes. Lysosomes are cellular organelles responsible for breaking down various molecules and cellular waste products. When lysosomes malfunction due to genetic mutations, they cannot perform their normal functions effectively. As a result, undigested substances accumulate within the lysosomes and disrupt cellular processes. This accumulation leads to a wide range of symptoms and organ damage, affecting multiple systems in the body. Most LSDs result from deficiencies of specific lysosomal enzymes. These enzymes are responsible for breaking down complex molecules, such as lipids (fats), glycoproteins, and mucopolysaccharides. When a particular enzyme is deficient or absent, the corresponding substrate accumulates within lysosomes. There are over 50 different LSDs, each associated with a specific lysosomal enzyme deficiency. Examples of LSDs include Gaucher's disease, Tay-Sachs disease, Fabry disease, Pompe disease, Niemann-Pick disease, and mucopolysaccharidoses (MPS). Each LSD has its unique clinical features and disease course. For instance, according to the National Institutes of Health (NIH), as of April 2022, Pompe disease affects approximately 1 in 40,000 individuals in the United States.

Key Market Drivers

Advances in Research and Development

Gene therapy has emerged as a promising approach for treating certain LSDs. Researchers are exploring methods to deliver functional genes into affected cells to restore enzyme production. Clinical trials and studies have shown promising results for diseases like mucopolysaccharidosis type II (Hunter syndrome) and Niemann-Pick disease type A and B. According to a July 2022 study published by the National Library of Medicine, lysosomal storage disorders (LSDs) are more prevalent when considered collectively, with a combined incidence of 1 in 5,000 to 1 in 8,000. The study highlights that ethnicity and geography influence LSD occurrence. For instance, Gaucher disease (GD) affects 1 in 40,000 to 1 in 60,000 in the general population but is significantly higher among Ashkenazi Jews (1 in 800). Similarly, Tay-Sachs disease (1 in 3,900), Niemann-Pick A, and mucolipidosis IV are more common in this group. In Finland, aspartylglucosaminuria occurs in 1 in 18,500 individuals. The increasing burden of LSDs is expected to drive market growth for lysosomal storage disease treatments in the coming years.

Small molecule chaperones are designed to stabilize mutant enzymes, allowing them to function more effectively. These therapies aim to correct the underlying enzymatic defects in LSDs. Some chaperone therapies have received regulatory approval and are available for patients with conditions like Fabry disease. Substrate Reduction Therapy (SRT) involves reducing the production of the toxic substrate that accumulates in lysosomes in LSDs. Medications like miglustat and eliglustat have been developed as SRTs and are used to treat diseases such as Gaucher's disease and Niemann-Pick type C. Ongoing research has led to the development of improved Enzyme Replacement Therapy (ERTs) with enhanced stability, bioavailability, and pharmacokinetics. These advancements aim to increase the effectiveness and convenience of treatment for patients with LSDs. Researchers are investigating the potential benefits of combining different therapeutic approaches, such as ERTs with chaperone therapies or gene therapy with small molecules. These combinations may offer synergistic effects and improved patient outcomes. Advances in biomarker research have led to the identification of specific markers that can aid in the diagnosis, monitoring, and assessment of disease progression in LSDs.

Key Market Challenges

Limited Understanding of Disease Mechanisms

In many LSDs, the underlying genetic and molecular mechanisms are complex and not fully understood. This complexity makes it challenging to develop targeted therapies that address the root cause of the disease. Without a comprehensive understanding of the disease mechanisms, it is difficult to identify specific drug targets and design effective treatments. LSDs encompass a wide range of rare genetic disorders, each with its unique pathophysiology. Understanding the variations in disease mechanisms among different LSDs is essential for developing tailored treatments. Limited knowledge of these variations can hinder therapeutic development efforts. Biomarkers are crucial for disease diagnosis, monitoring, and assessing treatment efficacy. However, without a deep understanding of disease mechanisms, it can be challenging to identify reliable biomarkers for LSDs, which are necessary for clinical trials and personalized medicine approaches. The lack of insight into disease mechanisms contributes to a high failure rate in drug development for LSDs. Many potential drug candidates do not progress past preclinical or early clinical stages because they do not effectively target the underlying disease processes. In the absence of a clear understanding of disease mechanisms, drug developers may face challenges related to off-target effects. These unintended consequences can lead to safety concerns and hinder the development of safe and effective therapies. The complexity of LSDs and the limited understanding of their mechanisms can make it difficult to secure research funding. Potential investors and grant providers may be hesitant to fund projects without a clear path to success, leading to underfunding of critical research efforts.

Key Market Trends

Chaperone Therapies

Chaperone therapies involve the use of small molecules that can stabilize and enhance the activity of misfolded or unstable lysosomal enzymes in LSDs. These molecules act as chaperones by assisting in the correct folding and trafficking of the enzyme to its target location within the lysosome. Chaperone therapies are designed to address the specific genetic mutations that lead to enzyme misfolding and dysfunction in LSDs. They target the underlying cause of the disease by helping the enzyme reach its active form, which is essential for substrate degradation. Many chaperone therapies are administered orally, which is a more convenient and patient-friendly route of administration compared to intravenous infusions or other invasive methods. This can improve treatment adherence and patient quality of life. Chaperone therapies have been developed and tested for various LSDs, including Fabry disease, Pompe disease, Gaucher's disease, and others. This broad applicability makes them relevant to multiple LSD subtypes. Some chaperone therapies have demonstrated clinical success and received regulatory approvals in different regions. For example, migalastat has been approved for the treatment of Fabry disease. Chaperone therapies hold the potential to modify the course of the disease by restoring enzyme activity and reducing substrate accumulation. This can lead to improvements in clinical outcomes and the prevention of disease progression. Researchers are exploring the possibility of combining chaperone therapies with other treatment approaches, such as enzyme replacement therapy (ERT) or gene therapy. These combination therapies may offer synergistic benefits and enhanced treatment efficacy. Chaperone therapies align with the trend toward personalized and precision medicine, where treatments are tailored to individual patients based on their specific genetic mutations and disease manifestations.

Key Market Players

• Pfizer, Inc.
• Sanofi SA
• BioMarin Pharmaceutical Inc
• Actelion Ltd.
• Raptor Pharmaceutical Corp.
• Protalix Biotherapeutics Inc.
• Amicus Therapeutics, Inc.
• Quest Diagnostics Inc.
• Amicus Therapeutics Inc.
• Shire Plc

Report Scope:

In this report, the Global Lysosomal Storage Diseases Therapeutics Market has been segmented into the following categories, in addition to the industry trends which have also been detailed below:

Lysosomal Storage Diseases Therapeutics Market, By Treatment:

• Enzyme Replacement Therapy
• Stem Cell Therapy
• Substrate Reduction Therapy
• Others

Lysosomal Storage Diseases Therapeutics Market, By Indication:

• Gaucher's Disease
• Fabry Disease
• Pompe's Syndrome
• Mucopolysaccharidosis
• Others

Lysosomal Storage Diseases Therapeutics Market, By End-User:

• Hospitals
• Clinics

Lysosomal Storage Diseases Therapeutics Market, By region:

• North America
  • United States
  • Canada
  • Mexico
• Asia-Pacific
  • China
  • India
  • South Korea
  • Australia
  • Japan
• Europe
  • Germany
  • France
  • United Kingdom
  • Spain
  • Italy
• South America
  • Brazil
  • Argentina
  • Colombia
• Middle East & Africa
  • South Africa
  • Saudi Arabia
  • UAE

Competitive Landscape

Company Profiles: Detailed analysis of the major companies present in the Global Lysosomal Storage Diseases Therapeutics Market.

Available Customizations:

Global Lysosomal Storage Diseases Therapeutics Market report with the given market data, TechSci Research offers customizations according to a company's specific needs. The following customization options are available for the report:

Company Information

• Detailed analysis and profiling of additional market players (up to five).

Table of Contents

1. Product Overview

• 1.1. Market Definition
• 1.2. Scope of the Market
  • 1.2.1. Markets Covered
  • 1.2.2. Years Considered for Study
  • 1.2.3. Key Market Segmentations

2. Research Methodology

• 2.1. Objective of the Study
• 2.2. Baseline Methodology
• 2.3. Key Industry Partners
• 2.4. Major Association and Secondary Sources
• 2.5. Forecasting Methodology
• 2.6. Data Triangulation & Validation
• 2.7. Assumptions and Limitations

3. Executive Summary

• 3.1. Overview of the Market
• 3.2. Overview of Key Market Segmentations
• 3.3. Overview of Key Market Players
• 3.4. Overview of Key Regions/Countries
• 3.5. Overview of Market Drivers, Challenges, Trends

4. Voice of Customer

5. Global Lysosomal Storage Diseases Therapeutics Market Outlook

• 5.1. Market Size & Forecast
  • 5.1.1. By Value
• 5.2. Market Share & Forecast
  • 5.2.1. By Treatment (Enzyme Replacement Therapy, Stem Cell Therapy, Substrate Reduction Therapy, others)
  • 5.2.2. By Indication (Gaucher's Disease, Fabry Disease, Pompe's Disease, Mucopolysaccharidosis, others)
  • 5.2.3. By End User (Hospitals, Clinics),
  • 5.2.4. By Region
  • 5.2.5. By Company (2024)
• 5.3. Market Map

6. Asia Pacific Lysosomal Storage Diseases Therapeutics Market Outlook

• 6.1. Market Size & Forecast
  • 6.1.1. By Value
• 6.2. Market Share & Forecast
  • 6.2.1. By Treatment
  • 6.2.2. By Indication
  • 6.2.3. By End User
  • 6.2.4. By Country
• 6.3. Asia Pacific: Country Analysis
  • 6.3.1. China Lysosomal Storage Diseases Therapeutics Market Outlook
    • 6.3.1.1. Market Size & Forecast
      • 6.3.1.1.1. By Value
    • 6.3.1.2. Market Share & Forecast
      • 6.3.1.2.1. By Treatment
      • 6.3.1.2.2. By Indication
      • 6.3.1.2.3. By End User
  • 6.3.2. India Lysosomal Storage Diseases Therapeutics Market Outlook
    • 6.3.2.1. Market Size & Forecast
      • 6.3.2.1.1. By Value
    • 6.3.2.2. Market Share & Forecast
      • 6.3.2.2.1. By Treatment
      • 6.3.2.2.2. By Indication
      • 6.3.2.2.3. By End User
  • 6.3.3. Australia Lysosomal Storage Diseases Therapeutics Market Outlook
    • 6.3.3.1. Market Size & Forecast
      • 6.3.3.1.1. By Value
    • 6.3.3.2. Market Share & Forecast
      • 6.3.3.2.1. By Treatment
      • 6.3.3.2.2. By Indication
      • 6.3.3.2.3. By End User
  • 6.3.4. Japan Lysosomal Storage Diseases Therapeutics Market Outlook
    • 6.3.4.1. Market Size & Forecast
      • 6.3.4.1.1. By Value
    • 6.3.4.2. Market Share & Forecast
      • 6.3.4.2.1. By Treatment
      • 6.3.4.2.2. By Indication
      • 6.3.4.2.3. By End User
  • 6.3.5. South Korea Lysosomal Storage Diseases Therapeutics Market Outlook
    • 6.3.5.1. Market Size & Forecast
      • 6.3.5.1.1. By Value
    • 6.3.5.2. Market Share & Forecast
      • 6.3.5.2.1. By Treatment
      • 6.3.5.2.2. By Indication
      • 6.3.5.2.3. By End User

7. Europe Lysosomal Storage Diseases Therapeutics Market Outlook

• 7.1. Market Size & Forecast
  • 7.1.1. By Value
• 7.2. Market Share & Forecast
  • 7.2.1. By Treatment
  • 7.2.2. By Indication
  • 7.2.3. By End User
  • 7.2.4. By Country
• 7.3. Europe: Country Analysis
  • 7.3.1. France Lysosomal Storage Diseases Therapeutics Market Outlook
    • 7.3.1.1. Market Size & Forecast
      • 7.3.1.1.1. By Value
    • 7.3.1.2. Market Share & Forecast
      • 7.3.1.2.1. By Treatment
      • 7.3.1.2.2. By Indication
      • 7.3.1.2.3. By End User
  • 7.3.2. Germany Lysosomal Storage Diseases Therapeutics Market Outlook
    • 7.3.2.1. Market Size & Forecast
      • 7.3.2.1.1. By Value
    • 7.3.2.2. Market Share & Forecast
      • 7.3.2.2.1. By Treatment
      • 7.3.2.2.2. By Indication
      • 7.3.2.2.3. By End User
  • 7.3.3. Spain Lysosomal Storage Diseases Therapeutics Market Outlook
    • 7.3.3.1. Market Size & Forecast
      • 7.3.3.1.1. By Value
    • 7.3.3.2. Market Share & Forecast
      • 7.3.3.2.1. By Treatment
      • 7.3.3.2.2. By Indication
      • 7.3.3.2.3. By End User
  • 7.3.4. Italy Lysosomal Storage Diseases Therapeutics Market Outlook
    • 7.3.4.1. Market Size & Forecast
      • 7.3.4.1.1. By Value
    • 7.3.4.2. Market Share & Forecast
      • 7.3.4.2.1. By Treatment
      • 7.3.4.2.2. By Indication
      • 7.3.4.2.3. By End User
  • 7.3.5. United Kingdom Lysosomal Storage Diseases Therapeutics Market Outlook
    • 7.3.5.1. Market Size & Forecast
      • 7.3.5.1.1. By Value
    • 7.3.5.2. Market Share & Forecast
      • 7.3.5.2.1. By Treatment
      • 7.3.5.2.2. By Indication
      • 7.3.5.2.3. By End User

8. North America Lysosomal Storage Diseases Therapeutics Market Outlook

• 8.1. Market Size & Forecast
  • 8.1.1. By Value
• 8.2. Market Share & Forecast
  • 8.2.1. By Treatment
  • 8.2.2. By Indication
  • 8.2.3. By End User
  • 8.2.4. By Country
• 8.3. North America: Country Analysis
  • 8.3.1. United States Lysosomal Storage Diseases Therapeutics Market Outlook
    • 8.3.1.1. Market Size & Forecast
      • 8.3.1.1.1. By Value
    • 8.3.1.2. Market Share & Forecast
      • 8.3.1.2.1. By Treatment
      • 8.3.1.2.2. By Indication
      • 8.3.1.2.3. By End User
  • 8.3.2. Mexico Lysosomal Storage Diseases Therapeutics Market Outlook
    • 8.3.2.1. Market Size & Forecast
      • 8.3.2.1.1. By Value
    • 8.3.2.2. Market Share & Forecast
      • 8.3.2.2.1. By Treatment
      • 8.3.2.2.2. By Indication
      • 8.3.2.2.3. By End User
  • 8.3.3. Canada Lysosomal Storage Diseases Therapeutics Market Outlook
    • 8.3.3.1. Market Size & Forecast
      • 8.3.3.1.1. By Value
    • 8.3.3.2. Market Share & Forecast
      • 8.3.3.2.1. By Treatment
      • 8.3.3.2.2. By Indication
      • 8.3.3.2.3. By End User

9. South America Lysosomal Storage Diseases Therapeutics Market Outlook

• 9.1. Market Size & Forecast
  • 9.1.1. By Value
• 9.2. Market Share & Forecast
  • 9.2.1. By Treatment
  • 9.2.2. By Indication
  • 9.2.3. By End User
  • 9.2.4. By Country
• 9.3. South America: Country Analysis
  • 9.3.1. Brazil Lysosomal Storage Diseases Therapeutics Market Outlook
    • 9.3.1.1. Market Size & Forecast
      • 9.3.1.1.1. By Value
    • 9.3.1.2. Market Share & Forecast
      • 9.3.1.2.1. By Treatment
      • 9.3.1.2.2. By Indication
      • 9.3.1.2.3. By End User
  • 9.3.2. Argentina Lysosomal Storage Diseases Therapeutics Market Outlook
    • 9.3.2.1. Market Size & Forecast
      • 9.3.2.1.1. By Value
    • 9.3.2.2. Market Share & Forecast
      • 9.3.2.2.1. By Treatment
      • 9.3.2.2.2. By Indication
      • 9.3.2.2.3. By End User
  • 9.3.3. Colombia Lysosomal Storage Diseases Therapeutics Market Outlook
    • 9.3.3.1. Market Size & Forecast
      • 9.3.3.1.1. By Value
    • 9.3.3.2. Market Share & Forecast
      • 9.3.3.2.1. By Treatment
      • 9.3.3.2.2. By Indication
      • 9.3.3.2.3. By End User

10. Middle East and Africa Lysosomal Storage Diseases Therapeutics Market Outlook

• 10.1. Market Size & Forecast
  • 10.1.1. By Value
• 10.2. Market Share & Forecast
  • 10.2.1. By Treatment
  • 10.2.2. By Indication
  • 10.2.3. By End User
  • 10.2.4. By Country
• 10.3. MEA: Country Analysis
  • 10.3.1. South Africa Lysosomal Storage Diseases Therapeutics Market Outlook
    • 10.3.1.1. Market Size & Forecast
      • 10.3.1.1.1. By Value
    • 10.3.1.2. Market Share & Forecast
      • 10.3.1.2.1. By Treatment
      • 10.3.1.2.2. By Indication
      • 10.3.1.2.3. By End User
  • 10.3.2. Saudi Arabia Lysosomal Storage Diseases Therapeutics Market Outlook
    • 10.3.2.1. Market Size & Forecast
      • 10.3.2.1.1. By Value
    • 10.3.2.2. Market Share & Forecast
      • 10.3.2.2.1. By Treatment
      • 10.3.2.2.2. By Indication
      • 10.3.2.2.3. By End User
  • 10.3.3. UAE Lysosomal Storage Diseases Therapeutics Market Outlook
    • 10.3.3.1. Market Size & Forecast
      • 10.3.3.1.1. By Value
    • 10.3.3.2. Market Share & Forecast
      • 10.3.3.2.1. By Treatment
      • 10.3.3.2.2. By Indication
      • 10.3.3.2.3. By End User

11. Market Dynamics

• 11.1. Drivers
• 11.2. Challenges

12. Market Trends & Developments

• 12.1. Recent Developments
• 12.2. Product Launches
• 12.3. Mergers & Acquisitions

13. Global Lysosomal Storage Diseases Therapeutics Market: SWOT Analysis

14. Porter's Five Forces Analysis

• 14.1. Competition in the Industry
• 14.2. Potential of New Entrants
• 14.3. Power of Suppliers
• 14.4. Power of Customers
• 14.5. Threat of Substitute Product

15. PESTLE Analysis

16. Competitive Landscape

• 16.1. Pfizer, Inc.
  • 16.1.1. Business Overview
  • 16.1.2. Company Snapshot
  • 16.1.3. Products & Services
  • 16.1.4. Financials (In case of listed companies)
  • 16.1.5. Recent Developments
  • 16.1.6. SWOT Analysis
• 16.2. Sanofi SA
  • 16.2.1. Business Overview
  • 16.2.2. Company Snapshot
  • 16.2.3. Products & Services
  • 16.2.4. Financials (In case of listed companies)
  • 16.2.5. Recent Developments
  • 16.2.6. SWOT Analysis
• 16.3. BioMarin Pharmaceutical Inc
  • 16.3.1. Business Overview
  • 16.3.2. Company Snapshot
  • 16.3.3. Products & Services
  • 16.3.4. Financials (In case of listed companies)
  • 16.3.5. Recent Developments
  • 16.3.6. SWOT Analysis
• 16.4. Actelion Ltd.
  • 16.4.1. Business Overview
  • 16.4.2. Company Snapshot
  • 16.4.3. Products & Services
  • 16.4.4. Financials (In case of listed companies)
  • 16.4.5. Recent Developments
  • 16.4.6. SWOT Analysis
• 16.5. Raptor Pharmaceutical Corp.
  • 16.5.1. Business Overview
  • 16.5.2. Company Snapshot
  • 16.5.3. Products & Services
  • 16.5.4. Financials (In case of listed companies)
  • 16.5.5. Recent Developments
  • 16.5.6. SWOT Analysis
• 16.6. Protalix Biotherapeutics Inc.
  • 16.6.1. Business Overview
  • 16.6.2. Company Snapshot
  • 16.6.3. Products & Services
  • 16.6.4. Financials (In case of listed companies)
  • 16.6.5. Recent Developments
  • 16.6.6. SWOT Analysis
• 16.7. Amicus Therapeutics, Inc.
  • 16.7.1. Business Overview
  • 16.7.2. Company Snapshot
  • 16.7.3. Products & Services
  • 16.7.4. Financials (In case of listed companies)
  • 16.7.5. Recent Developments
  • 16.7.6. SWOT Analysis
• 16.8. Quest Diagnostics Inc.
  • 16.8.1. Business Overview
  • 16.8.2. Company Snapshot
  • 16.8.3. Products & Services
  • 16.8.4. Financials (In case of listed companies)
  • 16.8.5. Recent Developments
  • 16.8.6. SWOT Analysis
• 16.9. Amicus Therapeutics Inc.
  • 16.9.1. Business Overview
  • 16.9.2. Company Snapshot
  • 16.9.3. Products & Services
  • 16.9.4. Financials (In case of listed companies)
  • 16.9.5. Recent Developments
  • 16.9.6. SWOT Analysis
• 16.10. Shire Plc
  • 16.10.1. Business Overview
  • 16.10.2. Company Snapshot
  • 16.10.3. Products & Services
  • 16.10.4. Financials (In case of listed companies)
  • 16.10.5. Recent Developments
  • 16.10.6. SWOT Analysis

17. Strategic Recommendations

18. About Us & Disclaimer