ÆÄºê¸®º´ Ä¡·á ½ÃÀå - ¼¼°è »ê¾÷ ±Ô¸ð, Á¡À¯À², µ¿Çâ, ±âȸ, ¿¹Ãø, ¾àÁ¦º°, Ä¡·áº°, Åõ¿© °æ·Îº°, À¯Åë ä³Îº°, Áö¿ªº° ºÎ¹®, °æÀï(2020-2030³â)
Fabry Disease Treatment Market - Global Industry Size, Share, Trends, Opportunity, and Forecast, Segmented By Drugs, By Treatment, By Route of Administration, By Distribution Channel, By Region & Competition, 2020-2030F
»óǰÄÚµå : 1691755
¸®¼­Ä¡»ç : TechSci Research
¹ßÇàÀÏ : 2025³â 03¿ù
ÆäÀÌÁö Á¤º¸ : ¿µ¹® 180 Pages
 ¶óÀ̼±½º & °¡°Ý (ºÎ°¡¼¼ º°µµ)
US $ 4,500 £Ü 6,279,000
Unprintable PDF (Single User License) help
PDF º¸°í¼­¸¦ 1¸í¸¸ ÀÌ¿ëÇÒ ¼ö ÀÖ´Â ¶óÀ̼±½ºÀÔ´Ï´Ù. Àμ⠺Ұ¡´ÉÇϸç, ÅØ½ºÆ®ÀÇ Copy&Pasteµµ ºÒ°¡´ÉÇÕ´Ï´Ù.
US $ 5,500 £Ü 7,674,000
PDF and Excel (Multi-User License) help
PDF ¹× Excel º¸°í¼­¸¦ ±â¾÷ÀÇ ÆÀÀ̳ª ±â°ü¿¡¼­ ÀÌ¿ëÇÒ ¼ö ÀÖ´Â ¶óÀ̼±½ºÀÔ´Ï´Ù. Àμ⠰¡´ÉÇϸç Àμ⹰ÀÇ ÀÌ¿ë ¹üÀ§´Â PDF ¹× Excel ÀÌ¿ë ¹üÀ§¿Í µ¿ÀÏÇÕ´Ï´Ù.
US $ 8,000 £Ü 11,163,000
PDF and Excel (Custom Research License) help
PDF ¹× Excel º¸°í¼­¸¦ µ¿ÀÏ ±â¾÷ÀÇ ¸ðµç ºÐÀÌ ÀÌ¿ëÇÒ ¼ö ÀÖ´Â ¶óÀ̼±½ºÀÔ´Ï´Ù. Àμ⠰¡´ÉÇϸç Àμ⹰ÀÇ ÀÌ¿ë ¹üÀ§´Â PDF ¹× Excel ÀÌ¿ë ¹üÀ§¿Í µ¿ÀÏÇÕ´Ï´Ù. 80½Ã°£ÀÇ ¾Ö³Î¸®½ºÆ® ŸÀÓÀÌ Æ÷ÇԵǾî ÀÖ°í Copy & Paste °¡´ÉÇÑ PPT ¹öÀüµµ Á¦°øµË´Ï´Ù. ªÀº Bespoke ¸®¼­Ä¡ ÇÁ·ÎÁ§Æ® ¼öÇà¿¡ ¸Â´Â ¶óÀ̼±½ºÀÔ´Ï´Ù.


¤± Add-on °¡´É: °í°´ÀÇ ¿äû¿¡ µû¶ó ÀÏÁ¤ÇÑ ¹üÀ§ ³»¿¡¼­ CustomizationÀÌ °¡´ÉÇÕ´Ï´Ù. ÀÚ¼¼ÇÑ »çÇ×Àº ¹®ÀÇÇØ Áֽñ⠹ٶø´Ï´Ù.

Çѱ۸ñÂ÷

¼¼°è ÆÄºê¸®º´ Ä¡·á ½ÃÀåÀº 2024³â 18¾ï 6,000¸¸ ´Þ·¯·Î Æò°¡µÇ¾ú°í, 2030³â±îÁö 6.30%ÀÇ ¿¬Æò±Õ º¹ÇÕ ¼ºÀå·ü(CAGR)À» ³ªÅ¸³»¸ç ¿¹Ãø ±â°£ µ¿¾È °ý¸ñÇÒ ¸¸ÇÑ ¼ºÀåÀ» ÀÌ·ê °ÍÀ¸·Î ¿¹»óµË´Ï´Ù.

ÆÐºê¸®º´Àº ¾Ø´õ½¼ ÆÐºê¸®º´À¸·Îµµ ¾Ë·ÁÁ® ÀÖÀ¸¸ç, ¸®¼ÒÁ» ÀúÀå Àå¾Ö·Î ¾Ë·ÁÁø Áúȯ±º¿¡ ¼ÓÇÏ´Â Èñ±ÍÇÑ À¯Àü¼º ÁúȯÀÔ´Ï´Ù. ÀÌ ÁúȯÀº ¥á-°¥¶ôÅä½Ã´Ù¾ÆÁ¦ A(¥á-Gal A)¶ó´Â È¿¼Ò¸¦ ¾ÏȣȭÇÏ´Â GLA À¯ÀüÀÚÀÇ µ¹¿¬º¯ÀÌ·Î ÀÎÇØ ¹ß»ýÇÕ´Ï´Ù. ÀÌ È¿¼Ò°¡ °áÇÌµÇ¸é ±Û·Îº¸Æ®¸®¾Æ¿À½Ç¼¼¶ó¹Ìµå(Gb3 ¶Ç´Â GL-3)·Î ¾Ë·ÁÁø ƯÁ¤ À¯ÇüÀÇ Áö¹æ ¹°ÁúÀÌ Àü½Å ¼¼Æ÷¿¡ ÃàÀûµË´Ï´Ù. ÀÌ Gb3ÀÇ ÃàÀûÀº ÁÖ·Î Ç÷°ü, ½ÅÀå, ½ÉÀå, ½Å°æ°è ¼¼Æ÷¿¡ ¿µÇâÀ» ¹ÌÃÄ ´Ù¾çÇÑ Áõ»ó°ú ÇÕº´ÁõÀ» À¯¹ßÇÕ´Ï´Ù. ÆÐºê¸®º´ÀÇ Áõ»óÀº ´ëºÎºÐ ¼Ò¾Æ±â ¶Ç´Â û¼Ò³â±â¿¡ ³ªÅ¸³ªÁö¸¸, Áõ»óÀÇ ¹ßÇö ¿¬·É°ú ÁßÁõµµ´Â ȯÀÚ¿¡ µû¶ó ¸Å¿ì ´Ù¾çÇÕ´Ï´Ù. ÆÄºê¸®º´ÀÇ Æ¯Â¡ÀûÀÎ Áõ»ó Áß Çϳª´Â ½Å°æº´Áõ¼º ÅëÁõÀ¸·Î ½É°¢ÇÏ°í ¸¸¼ºÈ­µÉ ¼ö ÀÖ½À´Ï´Ù. ÀÌ ÅëÁõÀº º¸Åë ¼ÕÀ̳ª ¹ß°ú °°Àº »çÁö¿¡ ¹ß»ýÇϸç, Á¾Á¾ ÀÛ¿­°¨À̳ª ÅëÁõÀ¸·Î Ç¥ÇöµË´Ï´Ù. ¿¹¸¦ µé¾î, ¹Ì±¹ ÆÄºê¸®º´ Àç´Ü(NFDF)¿¡ µû¸£¸é ¹Ì±¹¿¡¼­´Â ¸Å³â 4¿ùÀ» ÆÄºê¸®º´ ÀνÄÀÇ ´Þ·Î ÁöÁ¤Çϰí ÀÖ½À´Ï´Ù. ÀÎ½Ä Á¦°í ÇÁ·Î±×·¥Àº ÀÏ¹Ý ½Ã¹Î, ȯÀÚ, °£º´ÀÎ, ÀÇ·á Àü¹®°¡µéÀÇ ±³À°¿¡ ÃÊÁ¡À» ¸ÂÃß¾ú½À´Ï´Ù. ÀÌ·¯ÇÑ ÀÌ´Ï¼ÅÆ¼ºê´Â ÆÄºê¸®º´¿¡ ´ëÇÑ ÀÌÇØ, Áø´Ü ¹× °ü¸®¸¦ °³¼±ÇÏ´Â °ÍÀ» ¸ñÇ¥·Î Çϸç, ±Ã±ØÀûÀ¸·Î ¿¬±¸ ±â°£ µ¿¾È ½ÃÀå ¼ºÀå¿¡ ±â¿©ÇÒ °ÍÀÔ´Ï´Ù.

½ÃÀå °³¿ä
¿¹Ãø ±â°£ 2026-2030³â
½ÃÀå ±Ô¸ð : 2024³â 18¾ï 6,000¸¸ ´Þ·¯
½ÃÀå ±Ô¸ð : 2030³â 26¾ï 6,000¸¸ ´Þ·¯
CAGR : 2025-2030³â 6.30%
±Þ¼ºÀå ºÎ¹® ¿Â¶óÀÎ ¾à±¹
ÃÖ´ë ½ÃÀå ºÏ¹Ì

½ÃÀå ¼ºÀå ÃËÁø¿äÀÎ

Áø´ÜÀÇ ¹ßÀü

ÁÖ¿ä ½ÃÀå À̽´

Á¦ÇÑµÈ È¯ÀÚ ¼ö

ÁÖ¿ä ½ÃÀå µ¿Çâ

¹ÙÀÌ¿À¸¶Ä¿ °³¹ß

¸ñÂ÷

Á¦1Àå °³¿ä

Á¦2Àå Á¶»ç ¹æ¹ý

Á¦3Àå ÁÖ¿ä ¿ä¾à

Á¦4Àå °í°´ÀÇ ¼Ò¸®

Á¦5Àå ¼¼°èÀÇ ÆÄºê¸®º´ Ä¡·á ½ÃÀå Àü¸Á

Á¦6Àå ¾Æ½Ã¾ÆÅÂÆò¾çÀÇ ÆÄºê¸®º´ Ä¡·á ½ÃÀå Àü¸Á

Á¦7Àå À¯·´ÀÇ ÆÄºê¸®º´ Ä¡·á ½ÃÀå Àü¸Á

Á¦8Àå ºÏ¹ÌÀÇ ÆÄºê¸®º´ Ä¡·á ½ÃÀå Àü¸Á

Á¦9Àå ³²¹ÌÀÇ ÆÄºê¸®º´ Ä¡·á ½ÃÀå Àü¸Á

Á¦10Àå Áßµ¿ ¹× ¾ÆÇÁ¸®Ä«ÀÇ ÆÄºê¸®º´ Ä¡·á ½ÃÀå Àü¸Á

Á¦11Àå ½ÃÀå ¿ªÇÐ

Á¦12Àå ½ÃÀå µ¿Çâ°ú ¹ßÀü

Á¦13Àå ¼¼°èÀÇ ÆÄºê¸®º´ Ä¡·á ½ÃÀå : SWOT ºÐ¼®

Á¦14Àå PorterÀÇ Five Forces ºÐ¼®

Á¦15Àå PESTEL ºÐ¼®

Á¦16Àå °æÀï ±¸µµ

Á¦17Àå Àü·«Àû Á¦¾È

Á¦18Àå ¸®¼­Ä¡»ç¿¡ ´ëÇØ & ¸éÃ¥»çÇ×

LSH
¿µ¹® ¸ñÂ÷

¿µ¹®¸ñÂ÷

Global Fabry Disease Treatment Market was valued at USD 1.86 billion in 2024 and is anticipated to witness an impressive growth in the forecast period with a CAGR of 6.30% through 2030. Fabry disease, also known as Anderson-Fabry disease, is a rare and inherited genetic disorder that belongs to a group of conditions known as lysosomal storage disorders. This disease is caused by mutations in the GLA gene, which encodes an enzyme called alpha-galactosidase A (alpha-Gal A). The deficiency of this enzyme results in the accumulation of a specific type of fatty substance, known as globotriaosylceramide (Gb3 or GL-3), within cells throughout the body. This buildup of Gb3 primarily affects the cells of blood vessels, kidneys, heart, and nervous system, leading to a wide range of symptoms and complications. Symptoms of Fabry disease often appear in childhood or adolescence, although the age of symptom onset and their severity can vary widely among affected individuals. One of the hallmark symptoms of Fabry disease is neuropathic pain, which can be severe and chronic. This pain typically affects the extremities, such as the hands and feet, and is often described as burning or tingling. For instance, according to the National Fabry Disease Foundation (NFDF) designates April as Fabry Disease Awareness Month each year in the United States. Awareness programs focus on educating the public, patients, caregivers, and healthcare professionals. These initiatives aim to improve the understanding, diagnosis, and management of Fabry disease, ultimately contributing to market growth throughout the study period.

Market Overview
Forecast Period2026-2030
Market Size 2024USD 1.86 Billion
Market Size 2030USD 2.66 Billion
CAGR 2025-20306.30%
Fastest Growing SegmentOnline Pharmacies
Largest MarketNorth America

Key Market Drivers

Advancements in Diagnosis

Genetic testing has become a cornerstone in the diagnosis of Fabry disease. Advances in genetic sequencing technology have made it more accessible and cost-effective to identify specific mutations in the GLA gene, which is responsible for the disease. Genetic testing can confirm the presence of Fabry disease and provide information about the specific genetic mutations involved. In some regions, newborn screening programs have been implemented to identify Fabry disease in infants shortly after birth. This early detection allows for prompt intervention and treatment, potentially preventing or delaying the onset of symptoms and organ damage. Researchers have been investigating biomarkers associated with Fabry disease. Biomarkers are measurable substances in the body that can indicate the presence of a disease or its progression. Biomarker research can aid in early diagnosis and monitoring the effectiveness of treatment. Clinical diagnostic criteria for Fabry disease have been refined and standardized. Healthcare professionals now have clearer guidelines and criteria to assist in diagnosing disease based on clinical symptoms and genetic testing results. For instance, in December 2022, Bio Sidus SA sponsored a clinical trial to assess the efficacy and safety of AGA BETA BS in FD patients previously stabilized with Fabrazyme. Also, Fabry disease pipeline products continue to drive market growth. For example, in August 2021, the European Commission approved Amicus Therapeutics' Galafold for long-term treatment of Fabry disease in patients aged 12 and above with an amenable mutation.

Key Market Challenges

Limited Patient Population

The small patient population with Fabry disease results in a limited market size for pharmaceutical companies. This can make it less economically attractive for these companies to invest in research and development of treatments for disease. Developing and gaining regulatory approval for new treatments, including clinical trials and research, is costly. In the case of rare diseases like Fabry disease, the small number of potential patients can make it challenging to recoup these expenses. Due to the small market size, the revenue potential for treatments for Fabry disease may be limited compared to drugs for more common conditions. This can affect the profitability of drug development efforts. Limited patient populations can result in challenges related to patient access to treatments and affordability. Even if effective treatments exist, they may not be accessible to all patients due to cost or availability. The rarity of Fabry disease can lead to delayed diagnosis or misdiagnosis, as healthcare providers may not be familiar with the condition. This can result in patients not receiving appropriate treatment until the disease has progressed. Limited patient populations can also result in a scarcity of clinical data on the disease and its treatment. This can make it challenging for healthcare providers to make informed treatment decisions. Recognizing the challenges posed by rare diseases, some regulatory agencies provide incentives for orphan drug development. These incentives can include extended market exclusivity and reduced regulatory fees.

Key Market Trends

Biomarker Development

Biomarkers can aid in the early diagnosis of Fabry disease, allowing for timely intervention and treatment initiation. Early diagnosis is essential for preventing or delaying the onset of symptoms and organ damage. Biomarkers can be used to monitor disease progression and assess the effectiveness of treatment over time. This enables healthcare providers to tailor treatment plans to individual patients' needs. Certain biomarkers may be associated with the severity of Fabry disease. Identifying these biomarkers can help predict disease outcomes and guide treatment decisions. Biomarkers can help determine how well a patient is responding to treatment. If treatment is effective, biomarkers may show improvements in disease-related indicators. Biomarkers can serve as valuable endpoints in clinical trials of new Fabry disease treatments. They provide objective measures of treatment efficacy and safety. The development of biomarkers supports the concept of personalized medicine, where treatments are tailored to individual patients based on their biomarker profiles. This approach can optimize treatment outcomes. Biomarkers provide insights into the underlying molecular and genetic mechanisms of Fabry disease. This knowledge can inform drug development efforts, leading to more targeted and effective therapies. Biomarkers can be used to stratify Fabry disease patients into different subgroups based on disease characteristics. This stratification can guide treatment decisions and improve patient outcomes. Biomarkers can help reduce diagnostic delays by providing objective evidence of Fabry disease. This is particularly important because Fabry disease is often underdiagnosed or misdiagnosed.

Key Market Players

Report Scope:

In this report, the Global Fabry Disease Treatment Market has been segmented into the following categories, in addition to the industry trends which have also been detailed below:

Fabry Disease Treatment Market, By Drugs:

Fabry Disease Treatment Market, By Treatment:

Fabry Disease Treatment Market, By Route of Administration:

Fabry Disease Treatment Market, By Distribution Channel:

Fabry Disease Treatment Market, By region:

Competitive Landscape

Company Profiles: Detailed analysis of the major companies present in the Global Fabry Disease Treatment Market.

Available Customizations:

Global Fabry Disease Treatment 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

Table of Contents

1. Product Overview

2. Research Methodology

3. Executive Summary

4. Voice of Customer

5. Global Fabry Disease Treatment Market Outlook

6. Asia Pacific Fabry Disease Treatment Market Outlook

7. Europe Fabry Disease Treatment Market Outlook

8. North America Fabry Disease Treatment Market Outlook

9. South America Fabry Disease Treatment Market Outlook

10. Middle East and Africa Fabry Disease Treatment Market Outlook

11. Market Dynamics

12. Market Trends & Developments

13. Global Fabry Disease Treatment Market: SWOT Analysis

14. Porter's Five Forces Analysis

15. PESTLE Analysis

16. Competitive Landscape

17. Strategic Recommendations

18. About Us & Disclaimer

(ÁÖ)±Û·Î¹úÀÎÆ÷¸ÞÀÌ¼Ç 02-2025-2992 kr-info@giikorea.co.kr
¨Ï Copyright Global Information, Inc. All rights reserved.
PC¹öÀü º¸±â