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Gene Therapies For Rare Diseases Market Addressing Unmet Needs: Gene Therapies for Rare Diseases Market Poised for Expansion

06-19-2024 02:29 AM CET | Advertising, Media Consulting, Marketing Research

Press release from: InsightAce Analytic Pvt.Ltd

/ PR Agency: InsightAce Analytic Pvt.Ltd
Gene Therapies For Rare Diseases Market Addressing Unmet Needs:

Gene Therapies For Rare Diseases Market worth $ 11.4 Billion by 2030 - Exclusive Report by InsightAcea Analytic

InsightAce Analytic Pvt. Ltd. announces the release of a market assessment report on the "Global Gene Therapies For Rare Diseases Market- by Product (Zolgensma, Invossa K, Strimvelis, Neovasculgen, Glybera, Luxturna, Zynteglo and Others), Disease Type (Hemophilia, Duchenne Muscular Dystrophy,

Achromatopsia, Cystic Fibrosis, Inherited Retinal Dystrophy, Fragile X Syndrome, Friedreich ataxia, Alpha-1 Antitrypsin Deficiency, Paroxysmal Nocturnal Hemoglobinuria, Retinitis Pigmentosa and Others), Trends, Industry Competition Analysis, Revenue and Forecast To 2030."

Get a free sample copy of the report: https://www.insightaceanalytic.com/request-sample/1091

According to the latest research by InsightAce Analytic, the global Gene Therapies For Rare Diseases market is expected to reach US$ 11,441.6 Million by 2030, with a CAGR of 21.7% during a forecast period of 2024-2031.

Gene Therapy: A Promising Approach for Rare Diseases
Gene therapy offers a revolutionary approach to treating rare diseases, which affect millions globally. Approximately 80% of rare diseases have a genetic basis, making gene therapy a highly targeted and potentially curative option. Unlike conventional treatments that often require continuous management, gene therapy holds the promise of single-dose interventions with long-lasting benefits for patients.

Factors Driving Market Growth
The market for gene therapy for rare diseases is experiencing significant growth fueled by several factors:

• Rising Prevalence of Rare Diseases: The increasing incidence of rare diseases and the associated healthcare burden are driving demand for effective treatments.

• Novel Gene Therapies: The development of new gene therapies for various rare diseases is expanding treatment options for patients.

• Expanding Gene Therapy Pipelines: The growth of gene therapy pipelines, with numerous therapies under development, indicates a promising future for the market.

• Increasing Drug Approvals: The growing number of regulatory approvals for gene therapies is accelerating their adoption by healthcare providers.

• Improved Healthcare Access: Rising healthcare access and affordability in developing regions are leading to more patients seeking treatment for rare diseases.

• Technological Advancements: Rapid advancements in gene therapy technologies specifically designed for rare diseases are creating significant market potential.

• Growing Research Focus: Increased emphasis on research initiatives and the development of innovative gene therapies are driving market growth.

• Supportive Government Policies: Positive government measures to raise awareness of gene therapies and facilitate access to effective treatments are further propelling market expansion.

I hope this revision improves readability by separating the explanation of gene therapy for rare diseases from the market analysis and highlighting the specific factors driving growth.

North America is anticipated to contribute to the Gene Therapies For Rare Diseases market. The market for gene therapies for rare diseases is expanding due to increased healthcare spending, which has fueled the growth of research organizations in the area. Growing numbers of regional government initiatives are also influencing industry growth tendencies.

In addition, the Asia Pacific Gene Therapies For Rare Diseases market is expected to register significant growth due to the country's expanding biomedical and regenerative medicine research. The establishment has accelerated the discovery of novel medicines for the treatment of rare diseases by the Japanese government of support networks and special regulatory authorities.

Major market players operating in the Gene Therapies For Rare Diseases market include
4d Molecular Therapeutics, LLC, Abeona Therapeutics Inc., Advaxis, Adverum Biotech, Aevi Genomic, Applied Genetic Technologies Corporation (AGTC), Alcyone Lifesciences, Allife Medical Science and Technology, Amarna Therapeutics, American Gene Technologies, Amgen, Amicus Therapeutics, Anchiano Therapeutics, AnGes MG, Apic Bio, Armata Pharmaceuticals, Arrowhead, Arthrogen, Asklepios, Astellas, AVROBIO, BCM Families Foundation, Beijing Northland, Benitec, Biogen, BioMarin, Biosidus, bluebird bio, Boryung Group, Brain Neurotherapeuticsy Bio, Celsion Corporation, Chiesi, CRISPR Therapeutics, CSL

Behring, Daewoong Pharma, Dicerna, Editas Medicine, Eiger BioPharmaceuticals, Enzo Therapeutics, Esteve, Evox Therapeutics, Expression Therapeutics, Fibrocell, Flexion Therapeutics,, Fortress Biotech, Freeline Therapeutics, Gene Biotherapeutics, Genenta Science, GeneQuine, Genethon, GenSight, Gilead, Gradalis, GSK, Hanugen, Helixmith, Herantis, ID Pharma, Immusoft, Inovio, Intellia Therapeutics, Intrexon, J&J, Juventas, Kolon Life Science, Krystal Biotech, Locana, LogicBio Therapeutics,

Lysogene, Medigene, MeiraGTx, Miltenyi Biotec, Molecular Templates, Momotaro-Gene, Neuralgene, Novartis, OncoSec, Orchard Therapeutics, Oxford Biomedica, Pfizer, Prevail Therapeutics, PTC Therapeutics, REGENXBIO, Renova Therapeutics, Reyon Pharmaceutical, Roche, Rocket Pharma, Roivant, Sangamo Therapeutics, Sarepta Therapeutics, Seelos Therapeutics, Solid BioSciences, Sterna Biologicals, Sutura Therapeutics, SynerGene, Takara, Takeda, Talee Bio, Theragene Pharma, Transgene, Ultragenyx, uniQure, VBL Therapeutics, Vertex, Voyager Therapeutics, Xalud, Xenon, and Ziopharm.

Recent collaborations and agreements in the market:
• In August 2019, Gaboxadol was developed, manufactured, and made widely available in the European market by the U.S. company Ovid Therapeutics in collaboration with the Italian company Angelini Pharma to treat Angelman condition, an uncommon hereditary illness.

Curious about this latest version of the report? Obtain Report Details @ https://www.insightaceanalytic.com/enquiry-before-buying/1091

Market Segments
Global Gene Therapies For Rare Diseases Market, by Product, 2022-2030 (Value US$ Mn)
• Zolgensma
• Invossa K
• Strimvelis
• Neovasculgen
• Glybera
• Luxturna
• Zynteglo
• Others

Global Gene Therapies For Rare Diseases Market, by Disease Type, 2022-2030 (Value US$ Mn)
• Hemophilia
• Duchenne Muscular Dystrophy
• Achromatopsia
• Cystic Fibrosis
• Inherited Retinal Dystrophy
• Fragile X Syndrome
• Friedreich ataxia
• Alpha-1 Antitrypsin Deficiency
• Paroxysmal Nocturnal Hemoglobinuria
• Retinitis Pigmentosa
• Others

Global Gene Therapies For Rare Diseases Market, by Region, 2022-2030 (Value US$ Mn)
• North America
• Europe
• Asia Pacific
• Latin America
• Middle East & Africa

North America Gene Therapies For Rare Diseases Market, by country, 2022-2030 (Value US$ Mn)
• U.S.
• Canada

Europe Gene Therapies For Rare Diseases Market, by Country, 2022-2030 (Value US$ Mn)
• Germany
• France
• Italy
• Spain
• Russia
• Rest of Europe

Asia Pacific Gene Therapies For Rare Diseases Market, by country, 2022-2030 (Value US$ Mn)
• India
• China
• Japan
• South Korea
• Australia & New Zealand

Latin America Gene Therapies For Rare Diseases Market, by country, 2022-2030 (Value US$ Mn)
• Brazil
• Mexico
• Rest of Latin America

Middle East & Africa Gene Therapies For Rare Diseases Market, by country, 2022-2030 (Value US$ Mn)
• GCC Countries
• South Africa
• Rest of Middle East & Africa

Why should buy this report:
 To receive a comprehensive analysis of the prospects for the global Gene Therapies For Rare Diseases market
 To receive an industry overview and future trends of the Gene Therapies For Rare Diseases market
 To analyze the Gene Therapies For Rare Diseases market drivers and challenges
 To get information on the Gene Therapies For Rare Diseases market value (US$ Mn) forecast to 2030
 Significant investments, mergers & acquisitions in the Gene Therapies For Rare Diseases market industry

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About Us:
InsightAce Analytic is a market research and consulting firm that enables clients to make strategic decisions.
Our qualitative and quantitative market intelligence solutions inform the need for market and competitive intelligence to expand businesses.
We help clients gain a competitive advantage by identifying untapped markets, exploring new and competing technologies, segmenting potential markets, and repositioning products.
Our expertise is in providing syndicated and custom market intelligence reports with an in-depth analysis with key market insights in a timely and cost-effective manner.

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