mRNA1345 (mRESVIA) | Imetelstat (Rytelo)| Forecast 2024–2033 | RNA Therapeutics Market Analysis — Analysis India

Introduction: RNA Therapies Moving to the Mainstream

Analysis India: Over the past decade, RNA-based medicines have shifted from being a scientific curiosity to a central pillar of modern healthcare. When the pandemic arrived, it did more than strain public health systems. It changed the way medicines are created and delivered. Messenger RNA (mRNA) vaccines went from early concept to global use in an exceptionally short time, proving that development and distribution could move faster than anyone expected. That breakthrough did not end with one disease. It opened the way for RNA science to reach into cancer care, treatments for rare conditions, and other areas that once seemed out of reach.

Vertical infographic titled The RNA Therapeutics Market showing global growth trends, key modalities (mRNA, RNAi, ASO), delivery innovations (LNPs, polymers), leading therapies, investment drivers, and regional dynamics with simple icons and a beige background.


Today, the global RNA therapeutics market is one of the fastest-growing segments of biotechnology. Industry watchers expect the RNA therapy market to grow at a healthy pace throughout the 2030s, driven by a deep pipeline of new drugs, better delivery methods, and increasing funding from public programs and private investors. Two examples that capture this momentum are mRNA1345 also known as mRESVIA which is Moderna’s vaccine for RSV, and Imetelstat also called Rytelo which targets telomerase in blood cancers. Together they show how advances in RNA are changing the direction of modern pharmaceuticals.

The RNA Therapeutics Market: Global Growth Trends

The RNA therapeutics market is expected to expand rapidly, with revenues projected to surpass US$ 20 Billion by the early 2030s. Several forces are driving this growth. First, the success of mRNA vaccines has increased trust among regulators, healthcare professionals, and patients. Second, the RNA drug pipeline is diversifying, with candidates targeting infectious diseases, cancers, and rare genetic conditions. Third, advances in RNA delivery technologies such as lipid nanoparticles have improved the stability and safety of these therapies. Finally, strong investment trends are fueling innovation, with venture capital, pharmaceutical giants, and governments all committing resources to RNA research and manufacturing.

North America holds the lead today because it has a well-developed biotech sector and regulatory frameworks that support innovation. Europe is not far behind with strong research hubs and healthcare systems. The fastest expansion is likely to come from the Asia Pacific region where healthcare spending is rising and populations are aging.

mRNA1345 (mRESVIA): Expanding the mRNA Vaccine Market

Why RSV Matters

Respiratory syncytial virus (RSV) causes a large share of respiratory illness worldwide, especially in infants, elderly people, and those with weakened immune systems. Until recently, there was no effective vaccine to prevent RSV infections, leaving healthcare systems vulnerable to seasonal surges. Moderna’s mRNA1345 (mRESVIA) is designed to change that.

Revenue Outlook

Forecasts suggest that mRESVIA will generate US$ 290 Million in 2024, rising to US$ 584 Million in 2025 and US$ 913 Million in 2026. By 2027, sales are expected to exceed US$ 1,251 Million, with revenues continuing to climb to US$ 2,330 Million by 2033. This trajectory highlights the rapid adoption curve typical of vaccines, especially those addressing high-burden diseases.

Bar chart of projected annual revenue for mRNA1345 (mRESVIA) from 2024 to 2033 in million US dollars, red bars with data labels above each bar and y-axis ticks at 500 million increments; source credited to Analysis India at the bottom center.

Market Drivers

The global demand for RSV vaccines is supported by demographic trends, particularly the aging populations of North America, Europe, and Japan. Seasonal vaccination programs, similar to influenza campaigns, are expected to ensure recurring demand. However, competition from Pfizer and GSK will influence pricing and market share. Even so, mRESVIA’s strong early uptake underscores the scalability of mRNA vaccine platforms in addressing global infectious disease challenges.

Imetelstat (Rytelo): RNA-Based Oncology Innovation

RNA in Cancer Therapy

While vaccines dominate public discussion, RNA-based oncology therapies are emerging as one of the most promising applications of RNA science. Imetelstat (Rytelo), developed by Geron Corporation, is a telomerase inhibitor designed to treat hematologic malignancies such as myelodysplastic syndromes and myelofibrosis. Imetelstat works by interfering with telomere maintenance, undermining a fundamental survival process in cancer cells and offering a new therapeutic approach.

 Revenue Outlook

Imetelstat’s revenue projections begin modestly, with US$ 76 Million dollars in 2024, rising to US$ 319 Million in 2025 and US$ 597 Million in 2026. By 2028, revenues are expected to surpass US$ 1.47 Billion, with continued growth to US$ 2.52 Billion by 2033. Unlike vaccines, which plateau after rapid adoption, oncology therapies like Rytelo show sustained long-term growth.

Sales projection graphic for Imetelstat (Rytelo) showing a stylized molecular icon, concise summary of therapeutic mechanism (telomere maintenance inhibition), and a projected revenue trendline or bar visual with a neutral color palette and Analysis India source credit.

Market Drivers

The oncology market is characterized by high unmet need, premium pricing, and long treatment durations. Imetelstat’s first-in-class status positions it as a potential game-changer in hematologic cancers. Its growth trajectory reflects the cautious but steady adoption typical of oncology therapies. If Imetelstat succeeds commercially it could transform Geron and reshape the company’s strategic prospects.

RNA Interference (RNAi) and Antisense Oligonucleotides (ASO)

The RNA therapeutics market extends beyond mRNA vaccines and oncology drugs and now includes approaches such as RNA interference and antisense oligonucleotides which are steadily gaining momentum. RNAi therapies silence disease-causing genes, while ASOs target genetic mutations at the RNA level. Both approaches are showing promise in treating rare genetic disorders like spinal muscular atrophy and hereditary liver diseases.

These treatments demonstrate how flexible RNA science is and how it can tackle diseases that once had no effective therapies.

RNA Delivery Technologies: Unlocking Market Potential

One of the most critical factors in the success of RNA therapies is the advancement of RNA delivery technologies. Advances in delivery methods like lipid nanoparticles and polymer carriers are making RNA medicines more stable, safer, and more effective. These delivery innovations are essential for the global growth of the RNA medicine market.

Investment Trends in RNA Medicine

The surge in RNA innovation has attracted unprecedented levels of investment. Venture capitalists, large pharmaceutical companies, and government programs are investing heavily in RNA therapies and will help shape the sector over the next decade. Manufacturing infrastructure for RNA therapies is expanding globally, ensuring preparedness for future pandemics and supporting the commercialization of oncology and rare disease treatments.

For investors, the contrasting trajectories of mRESVIA and Rytelo illustrate the balance between rapid vaccine adoption and the durable growth of oncology therapies.

Regional Market Dynamics

North America

North America dominates the RNA therapeutics market, supported by strong R&D infrastructure, favorable regulatory frameworks, and high healthcare spending. The U.S. remains the largest single market for RNA therapies.

Europe

Europe remains a strong contender in the global RNA therapeutics landscape, with countries like Germany, the United Kingdom, and France leading the way in clinical adoption, regulatory approvals, and biotech investment. These nations benefit from robust healthcare systems, well-established pharmaceutical industries, and proactive regulatory agencies that have embraced RNA-based innovation. Their early support for RNA vaccines and therapies has positioned them as key players in shaping the future of RNA medicine across the continent. The European Medicines Agency has been proactive in approving RNA-based treatments, particularly in oncology and rare diseases.

Asia-Pacific

Asia-Pacific is expected to witness the fastest growth, driven by aging populations in Japan and China, rising healthcare investments, and expanding biotech ecosystems.

Emerging Markets

Emerging markets in Latin America, the Middle East, and Africa face challenges in accessing RNA therapies due to cost, but tiered pricing strategies and partnerships could expand their reach over time.

Future Outlook: The RNA Medicine Revolution

The future of the RNA medicine market is defined by diversity and innovation. From mRNA vaccines that prevent seasonal infections to RNA-based oncology therapies that extend survival in cancer patients, RNA is proving to be one of the most versatile platforms in modern medicine.

The global RNA therapeutics market will continue to expand as new therapies enter the pipeline, regulatory frameworks evolve, and delivery technologies improve. By the mid-2030s, RNA therapies are expected to be a standard part of healthcare systems worldwide.

Conclusion: RNA Therapies as a Global Healthcare Pillar

The stories of mRNA1345 (mRESVIA) and Imetelstat (Rytelo) illustrate two distinct but equally impactful paths in the RNA revolution. One showcases the rapid adoption of mRNA vaccines in infectious disease prevention, while the other highlights the sustained growth of RNA-based oncology therapies. Together, they demonstrate how the RNA therapeutics market is reshaping global healthcare, investment strategies, and patient outcomes.

As the world looks ahead, RNA therapies will not only define the next decade of pharmaceutical innovation but also establish themselves as a permanent pillar of modern medicine.

Frequently Asked Questions (FAQ) — The Global RNA Therapeutics Market

What is the scope of this report?
The report provides a market overview and 2024–2033 revenue forecasts for RNA therapeutics, with analysis of delivery technologies, investment trends, regional dynamics, and case studies of mRNA1345 (mRESVIA) and Imetelstat (Rytelo).
Which RNA modalities are covered?
The report covers mRNA vaccines, RNA interference (RNAi), antisense oligonucleotides (ASO), and other emerging RNA-based therapeutic approaches expanding beyond vaccines and oncology.
What is the forecast horizon?
The primary forecast horizon is 2024–2033, with annual revenue projections and scenario analysis covering market drivers and risks across that period.
What are the headline projections for mRNA1345 (mRESVIA)?
mRNA1345 (mRESVIA) is forecast to grow from about US$290 million in 2024 to over US$2.3 billion by 2033 based on adoption, pricing, and manufacturing scale assumptions.
How is Imetelstat (Rytelo) treated in the analysis?
Imetelstat is presented as an RNA-based oncology example where commercial success could transform a smaller biotech’s strategic prospects and, under favorable adoption and payer scenarios, generate material multi‑billion dollar revenues.
Which delivery technologies enable RNA medicines?
Lipid nanoparticles (LNPs), polymer-based carriers, and novel targeted delivery systems are identified as critical enablers that improve stability, safety, tissue targeting, and overall clinical utility.
Who is investing in RNA therapeutics?
Funding comes from venture capital firms, strategic investments by large pharmaceutical companies, and government programs supporting R&D, clinical development, and manufacturing scale-up.
Which regions lead and which will grow fastest?
North America leads current adoption; Europe (notably Germany, the UK, and France) follows closely; Asia‑Pacific is projected to record the fastest growth driven by rising healthcare investment and demographic trends.
What are the main commercial risks?
Key risks include clinical trial outcomes, regulatory timelines, manufacturing bottlenecks, pricing and reimbursement pressures, delivery safety issues, and competitive entrants that could alter adoption and revenue trajectories.
How should investors and strategists use this report?
Use it for scenario planning, portfolio prioritization, assessing manufacturing and supply chain needs, valuing platform versus product assets, and tracking regulatory and payer developments that influence commercialization paths.

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