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한글목차
아시아태평양의 핵산 치료제 CDMO 시장 규모는 2022년 9억 7,000만 달러에서 예측 기간 동안 13.92%의 CAGR을 나타내고, 2033년에는 40억 4,000만 달러 규모로 성장할 것으로 예상됩니다.
유전성 질환 및 만성 질환의 발병률 증가, 핵산 생산 개선, 규제 승인 증가, CDMO 제조 인프라 확대 등이 향후 몇 년동안 상당한 성장에 기여할 것으로 예상됩니다. 핵산 치료제에 대한 수요가 증가함에 따라 CDMO는 세계 환자들이 이러한 첨단 치료제를 이용할 수 있도록 하는 데 필수적인 요소로 여겨지고 있습니다.
아시아태평양의 핵산 치료제 CDMO 시장을 조사했으며, 시장 개요, 시장 성장에 영향을 미치는 각종 영향요인 분석, 시장 규모 추이 및 예측, 각종 부문별/지역별/주요 국가별 상세 분석, 경쟁 구도, 주요 기업 분석 등의 정보를 정리하여 전해드립니다.
주요 시장 통계
예측 기간
2023-2033년
2023년 평가
11억 달러
2033년 전망
40억 4,000만 달러
CAGR
13.92%
시장 구분 :
세분화 1: 화학합성 방법별
고체상 올리고뉴클레오티드 합성
액상 올리고뉴클레오티드 합성
세분화 2 : 국가별
중국
일본
인도
호주
기타 아시아태평양
목차
제1장 시장
세계 시장 전망
시장 개요
제품 정의
포함 기준과 제외 기준
주요 조사 결과
업계 전망
주요 동향
기회 평가
CDMO에 선호되는 기술
CDMO에의 아웃소싱에서 고려되는 요소
COVID-19가 세계 핵산 치료제 CDMO에 미치는 영향
현재의 핵산 치료제 CDMO 상황
치료제에서의 핵산 사용
치료제에 합성되는 핵산 유형
안티센스 올리고뉴클레오티드(ASO)와 DNA 압타머
RNA 간섭(RNAi)과 단쇄 간섭 RNA(siRNA)
마이크로 RNA(miRNA)
RNA 압타머와 RNA 디코이
리보자임
환형 RNA
사업 역학
영향 분석
사업 촉진요인
사업상 과제
사업 기회
제2장 핵산 치료제 CDMO 시장(지역별)
아시아태평양의 핵산 치료제 CDMO 시장
주요 조사 결과
시장 역학
시장 규모와 예측
제3장 시장 : 경쟁 벤치마킹 및 기업 개요
경쟁 벤치마킹
기업 개요
Asymchem Inc.
BioCina
CMIC HOLDINGS Co., Ltd.
Kaneka Corporation
Nippon Shkubai Co., Ltd
Nitto Group
ST Pharm
LSH
영문 목차
영문목차
“The Asia-Pacific Nucleic Acid Therapeutics CDMO Market Expected to Reach $4.04 Billion by 2033.”
KEY MARKET STATISTICS
Forecast Period
2023 - 2033
2023 Evaluation
$1.10 Billion
2033 Forecast
$4.04 Billion
CAGR
13.92%
Introduction to Asia-Pacific (APAC) Nucleic Acid Therapeutics CDMO Market
The APAC Nucleic Acid Therapeutics CDMO Market is expected to grow at a CAGR of 13.92% from $0.97 billion in 2022 to $4.04 billion by 2033 in the forecasted period of 2023-2033. The increasing incidence of hereditary and chronic illnesses, improvements in nucleic acid production, a rise in regulatory approvals, and an expanding CDMO manufacturing infrastructure are all expected to contribute to the significant growth of the APAC nucleic acid therapies CDMO market in the years to come. With the increasing demand for nucleic acid therapeutics, CDMOs will be essential in enabling patients all around the world to access these cutting-edge treatments.
Market Introduction
With the rising incidence of genetic and chronic illnesses, growing regulatory approvals, growing CDMO manufacturing infrastructure, and encouraging government initiatives, the APAC nucleic acid therapeutics CDMO market is expected to grow significantly in the next years. With the increasing demand for nucleic acid therapeutics, CDMOs will be essential in enabling patients all around the world to access these cutting-edge treatments.
Market Segmentation:
Segmentation 1: by Chemical Synthesis Method
Solid-Phase Oligonucleotide Synthesis
Liquid-Phase Oligonucleotide Synthesis
Segmentation 2: by Country
China
Japan
India
Australia
Rest-of-Asia-Pacific
Demand - Drivers and Limitations
The following are the drivers for the Asia-Pacific nucleic acid therapeutics CDMO market:
Increasing Presence of Established Players in the Region
Funding Support and Investments from the Government
Low Cost of Manufacturing
The market is expected to face some limitations as well due to the following challenges:
Lack of Expertise in Developing Nucleic Acid Therapeutics
How can this report add value to an organization?
Product/Innovation Strategy: The nucleic acid therapeutics CDMO market has been extensively segmented based on various categories, such as product, chemical synthesis method, disease type, technology, and end users. This can help readers get a clear overview of which segments account for the largest share and which ones are well-positioned to grow in the coming years.
Competitive Strategy: Key players in the Asia-Pacific nucleic acid therapeutics CDMO market analysed and profiled in the study involve established players that offer various kinds of nucleic acid therapeutics CDMO products.
The Asia-Pacific nucleic acid therapeutics CDMO market has witnessed several investments for the expansion of CDMO manufacturing units by the market players. The expansion is aimed at increasing the manufacturing capacity. To meet the growing demand for their services, CDMOs are expanding their manufacturing units and investing in new technologies. Additionally, comprehensive competitive strategies such as partnerships, agreements, and collaborations will aid the reader in understanding the untapped revenue pockets in the market.
Key Market Players and Competition Synopsis
The companies that are profiled have been selected based on inputs gathered from primary experts and analysing company coverage, product portfolio, and market penetration.
Some of the prominent names established in this market are:
Asymchem Inc.
BioCina
CMIC HOLDINGS Co., Ltd.
Kaneka Corporation
Nippon Shkubai Co., Ltd.
Nitto Group
ST Pharm
Table of Contents
1 Market
1.1 Global Market Outlook
1.1.1 Market Overview
1.1.2 Product Definition
1.1.3 Inclusion and Exclusion Criteria
1.1.4 Key Findings
1.2 Industry Outlook
1.2.1 Key Trends
1.2.1.1 Significant Number of Collaborations among Market Players
1.2.1.2 Increasing Investment for Expansion of Nucleic Acid Therapeutics CDMO Manufacturing Units
1.2.1.3 CDMOs Shifting their Business Strategy in Response to a Changing Environment
1.2.2 Opportunity Assessment
1.2.3 Preferred Techniques By CDMO
1.2.3.1 Preferred Techniques by CDMOs for Nucleic Acid Impurity Analysis
1.2.3.2 Preferred Techniques by CDMOs for Nucleic Acid Structural Analysis
1.2.3.3 Preferred Techniques by CDMOs for Nucleic Acid Purification
1.2.4 Factors Considered While Outsourcing To CDMO.
1.3 Impact of COVID-19 on the Global Nucleic Acid Therapeutics CDMO
1.3.1 Pre-COVID-19 Phase
1.3.2 During COVID-19
1.3.3 Post-COVID-19 Phase
1.3.3.1 Impact on Demand and Supply
1.4 Current Nucleic Acid Therapeutic CDMOs Landscape
1.5 Significant Usage of Nucleic Acid in Therapeutics
1.6 Types of Nucleic Acid Synthesized for Therapeutics
1.6.1 Anti-Sense Oligonucleotides (ASOs) and DNA Aptamers
1.6.2 RNA Interference (RNAi) and Short Interfering RNAs (siRNAs)
1.6.3 MicroRNAs (miRNAs)
1.6.4 RNA Aptamers and RNA Decoys
1.6.5 Ribozymes
1.6.6 Circular RNAs
1.7 Business Dynamics
1.7.1 Impact Analysis
1.7.2 Business Drivers
1.7.2.1 Growing Demand for Nucleic Acid Therapeutics Application to Treat Chronic and Genetic Diseases
1.7.2.2 Increasing FDA or European Medicines Agency (EMA) Approvals of Nucleic Acid Therapeutics
1.7.2.3 Advancements in Manufacturing Units for Producing Nucleic Acid by CDMOs
1.7.3 Business Restraints
1.7.3.1 Substantial Variations in Nucleic Acid Leading to Complications in Therapeutic Classification
1.7.3.2 Lack of Expertise in Developing Nucleic Acid Therapeutic
1.7.4 Business Opportunities
1.7.4.1 Continued Research and Development Activities for Manufacturing Innovative Nucleic Acid Therapeutics Forcing Pharmaceutical Companies to Expand their Businesses.
1.7.4.2 Pharmaceutical Firms Becoming More Outsourcing-Oriented
