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RNAi (RNA Interference) Technology Market to Reach US$ 6.63 Billion by 2033 at 10.4% CAGR; North America Leads with 41% Share - Key Players: Alnylam, Thermo Fisher Scientific, Merck KGaA

12-22-2025 08:37 AM CET | Health & Medicine

Press release from: DataM intelligence 4 Market Research LLP

RNAi (RNA interference) Technology

RNAi (RNA interference) Technology

The global RNAi (RNA interference) Technology Market reached US$ 2.75 billion in 2024, up from US$ 2.51 billion in 2023, and is expected to reach US$ 6.63 billion by 2033, growing at a CAGR of 10.4% during the forecast period 2025-2033. The market is expanding rapidly, driven by the clinical success of approved small interfering RNA (siRNA) therapeutics, significant advances in delivery technologies such as GalNAc conjugates and lipid nanoparticles, and rising investments through strategic partnerships between pharmaceutical and biotechnology companies.

North America currently dominates the market in terms of revenue due to strong R&D infrastructure, early adoption of advanced RNA-based therapies, and favorable regulatory support. Meanwhile, the Asia-Pacific region is expected to witness the fastest growth, supported by increasing research activities, expanding manufacturing capacity, and growing government and private-sector investments. The market outlook remains strong, particularly across applications in rare diseases, oncology, and metabolic disorders; however, challenges related to efficient extra-hepatic delivery, high development costs, and long regulatory timelines continue to pose key hurdles for broader commercialization.

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The RNAi (RNA interference) Technology Market is the sector that develops and commercializes RNA-based technologies and therapeutics to selectively silence gene expression for research and disease treatment.

Key Developments
✅ October 2025: U.S. biotechnology companies advanced late-stage clinical development of RNAi therapeutics targeting cardiometabolic, hepatic, and rare genetic disorders, supported by improved siRNA stability and delivery technologies.

✅ September 2025: European research institutions and pharma companies expanded use of GalNAc-conjugated RNAi platforms to enhance liver-specific targeting and dosing efficiency.

✅ August 2025: Asia-Pacific biotech firms increased investment in RNAi manufacturing scale-up, focusing on cost-efficient synthesis and large-scale production of siRNA therapeutics.

✅ July 2025: Global pharmaceutical companies integrated RNAi pipelines into broader precision medicine strategies, combining gene silencing therapies with genomic diagnostics.

✅ May 2025: North American developers leveraged lipid nanoparticle and next-generation delivery systems to improve tissue targeting and therapeutic durability of RNAi drugs.

✅ March 2025: Academic-industry collaborations worldwide accelerated preclinical RNAi research to expand applications in oncology, infectious diseases, and neurological disorders.

Mergers & Acquisitions
✅ November 2025: A U.S.-based pharmaceutical company acquired an RNAi-focused biotech firm to strengthen its gene-silencing therapeutic pipeline and precision medicine capabilities.

✅ August 2025: A European life sciences company entered a strategic partnership with an RNAi technology developer to co-develop next-generation siRNA therapeutics.

✅ June 2025: An Asia-Pacific RNAi startup was acquired by a global biopharmaceutical company to expand its RNA-based drug discovery and development platform.

Key Players
Alnylam Pharmaceuticals, Inc. | Thermo Fisher Scientific Inc. | Merck KGaA | Creative Biolabs | GenScript | Revvity | Promega Corporation | OriGene Technologies, Inc. | Altogen Biosystems

Key Highlights

Alnylam Pharmaceuticals, Inc. - Holds a share of 26.8%: Global leader in RNA interference (RNAi) therapeutics, with multiple approved siRNA drugs and strong expertise in GalNAc delivery platforms for rare genetic and cardiometabolic diseases.

Thermo Fisher Scientific Inc. - Holds a share of 18.4%: Provides comprehensive RNAi research tools, reagents, delivery systems, and analytical instruments supporting both academic research and therapeutic development.

Merck KGaA - Holds a share of 14.9%: Offers licensed RNAi technologies, reagents, and genome-editing solutions that enable gene-silencing research and drug discovery.

Creative Biolabs - Holds a share of 7.2%: Specializes in custom RNAi services, siRNA/shRNA design, and functional genomics studies for biopharmaceutical R&D.

GenScript - Holds a share of 9.6%: Delivers RNAi-related gene synthesis, vector construction, and screening services supporting drug discovery and validation workflows.

Revvity - Holds a share of 8.1%: Provides RNAi screening platforms, reagents, and high-throughput assay technologies for target identification and functional genomics.

Promega Corporation - Holds a share of 6.7%: Supplies RNAi-compatible assays and reagents used in gene expression analysis, target validation, and drug screening.

OriGene Technologies, Inc. - Holds a share of 5.4%: Focuses on RNAi vectors, gene silencing tools, and gene expression products for biomedical research.

Altogen Biosystems - Holds a share of 2.9%: Develops transfection reagents and delivery technologies optimized for siRNA and RNA-based therapeutics.

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Market Drivers
- Growing clinical success and regulatory approval of siRNA-based therapeutics for rare, genetic, and chronic diseases.

- Rising prevalence of genetic disorders, cancer, and metabolic diseases driving demand for targeted gene-silencing therapies.

- Advancements in RNA delivery technologies such as GalNAc conjugates and lipid nanoparticles improving efficacy and safety.

- Increasing investment in genomics, precision medicine, and RNA-based drug discovery.

- Strong academic and industry research activity supporting novel RNAi targets and applications.

- Expanding use of RNAi in functional genomics, target validation, and drug screening.

- Supportive regulatory pathways and orphan drug incentives accelerating RNAi therapy development.

Industry Developments
- Launch and commercialization of FDA-approved RNAi therapeutics for liver-related and rare diseases.

- Expansion of clinical pipelines with RNAi candidates targeting cardiovascular, metabolic, and neurological disorders.

- Strategic collaborations between biotech firms and large pharmaceutical companies to accelerate development and commercialization.

- Advances in chemical modification techniques to enhance RNA stability and reduce off-target effects.

- Increasing use of RNAi tools in research laboratories and biotechnology companies.

- Rising funding, partnerships, and acquisitions focused on RNA-based platforms and delivery systems.

- Development of next-generation RNAi platforms enabling tissue-specific and extrahepatic delivery.

Regional Insights
North America - 41% share: Driven by strong biotech and pharmaceutical presence, high R&D investment, and favorable regulatory environment.

Europe - 29% share: Supported by advanced research infrastructure, government funding for life sciences, and growing clinical trial activity.

Asia Pacific - 24% share: Fueled by expanding biotechnology sector, increasing genomic research, and rising healthcare investments.

Latin America - 4% share: Boosted by growing academic research and gradual adoption of advanced therapeutics.

Middle East & Africa - 2% share: Driven by emerging research initiatives and increasing focus on advanced biomedical technologies.

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Key Segments
By Product Type
siRNA (small interfering RNA) dominates the market due to its proven clinical efficacy and increasing number of approved therapies targeting genetic and chronic diseases. miRNA (microRNA) represents a growing segment, supported by expanding research into gene regulation and biomarker discovery. RNAi reagents and kits hold a significant share, driven by extensive use in research, drug discovery, and preclinical studies. Other RNAi-based products continue to support niche research and emerging therapeutic approaches.

By Therapeutic Application
Rare genetic disorders account for a substantial share of the market, supported by strong clinical success of RNAi therapies in addressing previously untreatable conditions. Oncology is a rapidly growing segment, driven by increasing research activity focused on targeted gene silencing and personalized cancer therapies. Cardiovascular and metabolic disorders represent a key application area due to rising disease prevalence and growing interest in RNA-based interventions. Neurological and neurodegenerative disorders are gaining momentum as advances in delivery technologies improve central nervous system targeting. Infectious diseases and other therapeutic areas continue to expand as RNAi platforms are explored for antiviral and emerging pathogen treatments.

By End-User
Pharmaceutical and biotechnology companies dominate the market owing to their strong investments in RNAi drug development, clinical trials, and commercialization efforts. Academic and research institutes hold a significant share, supported by extensive basic and translational research activities. Contract research organizations (CROs) and contract development and manufacturing organizations (CDMOs) are witnessing rapid growth as outsourcing of RNAi research, development, and manufacturing continues to increase. Other end users, including government and non-profit research organizations, contribute steadily to overall market demand.

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