Business Wire

MA-NOVOTECH

27.8.2024 13:06:28 CEST | Business Wire | Press release

Share
Transforming the Future of Medicine with RNA-Based Therapies

Novotech, the global full-service clinical Contract Research Organization (CRO) that partners with biotech companies to accelerate the development of advanced and novel therapeutics at every phase, has released its latest industry report, RNA Therapies — Global Clinical Trial Landscape (2024).

This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20240825825969/en/

This report details how RNA-based therapies have transitioned from a novel concept to an exciting frontier in modern medicine, demonstrating enormous potential for the treatment of diseases through highly-targeted mechanisms. It also provides a comprehensive overview of the current landscape, advancements, and future prospects of RNA therapeutics, focusing on their transformative impact on healthcare, and is available free of charge.

RNA therapies are at the forefront of medical advancements, poised to redefine the way we approach the treatment of some of the most challenging diseases known to humanity. RNA-based therapies offer a new frontier of therapeutic options with their versatility, effectiveness, and incredible adaptability.

The success of mRNA vaccines in the fight against COVID-19 was a clear example of how RNA therapies represented a practical option for large-scale development, as well as targeted medicine. The potential isn’t limited to vaccinations, but can also be used to combat infectious diseases, various types of cancers, and potentially offer an effective and economical way to address rare genetic disorders. The ability to target any gene in the human genome offers a breadth of potential far beyond what traditional therapies can currently achieve.

A factor that is of particular interest to medical research in RNA therapies is the unparalleled programmability. These are treatments that can be tailored with incredible precision, designed to target specific genetic markers and be modified rapidly to adapt to emerging challenges. The advancements in RNA delivery systems, such as lipid nanoparticles, are pushing the boundaries even further, ensuring that these therapies are not only effective but also safe and scalable.

The report touches on these major themes:

  • Versatility of RNA Therapies:
    • RNA-based therapies can target any gene, offering broad therapeutic potential beyond traditional drugs that focus solely on proteins.
    • They are “programmable drugs,” allowing for rapid and flexible production, akin to gene-modified cell therapies.
  • Success of mRNA Vaccines:
    • The COVID-19 pandemic showcased the power of mRNA technology, leading to its rapid development and global deployment.
    • The success of Pfizer and BioNTech's COVID-19 vaccine has set a precedent for further RNA-based vaccine developments targeting other infectious diseases, cancers, and metabolic disorders.
  • Clinical Trials and Global Landscape:
    • There has been significant growth in RNA therapy trials globally, with the Asia-Pacific region leading in trial growth rate.
    • The most common areas of application include infectious diseases, oncology, and rare genetic disorders.
  • Innovation in Delivery Methods:
    • Advancements in delivery technologies such as lipid nanoparticles (LNPs) have enhanced the stability and effectiveness of RNA therapies, reducing potential side effects.
  • Investment and Market Growth:
    • There has been a substantial increase in public and private funding for RNA research, particularly in the United States and China.
    • The market for RNA-based therapeutics is expected to grow significantly, driven by ongoing advancements and the successful application of these therapies in diverse areas.
  • Regulatory Landscape:
    • The FDA has approved over 20 RNA-based therapies, with many more in the pipeline, highlighting the evolving regulatory environment that is facilitating the rapid development of these treatments.
    • Many different entities are pursuing new RNA-based technologies, which has increased significantly since the rollout of the mRNA COVID-19 vaccine.

The report highlights how the field is poised for substantial growth, driven by significant advancements in technology, increased funding, and successful clinical outcomes. RNA therapies have the potential to play a significant role in advancing patient care and invites continued interest and investment in this rapidly evolving field.

For more information and to download the full report free of charge, please visit Novotech's website or contact our media relations team.

About Novotech Novotech-CRO.com

Founded in 1997, Novotech is a global full-service clinical Contract Research Organization (CRO) focused on partnering with biotech companies to accelerate the development of advanced and novel therapeutics at every phase.

Recognized for its industry-leading contributions, Novotech has received numerous prestigious awards, including the CRO Leadership Award 2023, the Asia Pacific Cell & Gene Therapy Clinical Trials Excellence 2023, the Asia-Pacific Contract Research Organization Company of the Year Award since 2006.

The Company offers a comprehensive suite of services including laboratories, Phase I facilities, drug development consulting, regulatory expertise, and has experience with over 5,000 clinical projects, including Phase I to Phase IV clinical trials and bioequivalence studies. With a presence in 34 office locations and a dedicated team of 3,000+ professionals worldwide, Novotech is a trusted end-to-end strategic partner of choice.

For more information or to speak to an expert team member visit www.Novotech-cro.com.

To view this piece of content from cts.businesswire.com, please give your consent at the top of this page.

View source version on businesswire.com: https://www.businesswire.com/news/home/20240825825969/en/

About Business Wire

Business Wire
Business Wire
101 California Street, 20th Floor
CA 94111 San Francisco

http://businesswire.com
DK

Subscribe to releases from Business Wire

Subscribe to all the latest releases from Business Wire by registering your e-mail address below. You can unsubscribe at any time.

Latest releases from Business Wire

Perpetual Atomics Ltd, QSA Europe, QSA Global and Reef Origin to Collaborate on Building Radioisotope Power Systems in Europe18.2.2026 16:44:00 CET | Press release

Perpetual Atomics Ltd, QSA Europe (a trading name of Loma Systems s.r.o.), QSA Global, Inc., and Reef Origin signed an MOU in Prague to collaborate on the industrialized production of radioisotope power systems in Europe. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260218036211/en/ Teams from Perpetual Atomics & QSA Global (USA and Czechia) at the facilities in Czechia This MOU builds on the existing collaboration between QSA Global, Inc. and Perpetual Atomics Ltd by expanding and strengthening the capacity and capability to produce radioisotope power systems in Europe. The key partnership with QSA Europe provides access to existing facilities, capabilities, knowledge, and know-how for the storage, handling, and distribution of commercial radioisotope systems for terrestrial applications. This capability is directly transferable to radioisotope power technologies for space. Radioisotope and nuclear power technologies are

Safe Software Launches FME Flow Availability in AWS Marketplace18.2.2026 15:00:00 CET | Press release

Today, Safe Software, the creator of FME, the All-Data, Any-AI enterprise integration platform with true support for spatial data, announced that FME Flow is now available in AWS Marketplace, which helps organizations easily discover, try, test, buy, deploy and manage thousands of software solutions, including pre-built AI agents and ready-to-integrate tools, all in one convenient destination. Amazon Web Services (AWS) customers can now purchase FME Flow directly within AWS Marketplace, simplifying billing and procurement and providing faster access to Safe Software’s enterprise-grade data automation capabilities. Safe Software’s FME connects all data across data velocities, locations, and types. FME Flow delivers many data workflow services to enterprise users. Availability in AWS Marketplace allows organizations to streamline the purchase and management of FME Flow directly within their AWS Marketplace account. “As the data landscape becomes increasingly complex and distributed, flex

Cubic Corporation Optimizes SAP Support with Rimini Street to Accelerate Modernization18.2.2026 15:00:00 CET | Press release

Adopting a composable ERP strategy with the support of Rimini Street, Cubic maintains SAP ECC as a stable core while pursuing modernization and automation initiatives across its broader application landscape — without the need for costly, disruptive upgrades Rimini Street, Inc. (Nasdaq: RMNI), the Software Support and Agentic AI ERP Company™, and the leading third-party support provider for Oracle, SAP and VMware software, today announced Cubic Corporation, innovation technology provider for the defense and transportation industry, has partnered with Rimini Street to support its strategy to modernize while maintaining SAP ECC as a stable core and to explore AI and automation initiatives across its broader application landscape. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260218871248/en/ Cubic Corporation Optimizes SAP Support with Rimini Street to Accelerate Modernization The strategy to forgo an expensive upgrade to S/4

FDA Approval Granted for Commercial Manufacturing at Rezon Bio's Warsaw-Duchnice Facility18.2.2026 14:01:00 CET | Press release

Rezon Bio announces that its Warsaw-Duchnice facility has received approval from the U.S. Food and Drug Administration (FDA) for the commercial manufacturing of a biosimilar. This milestone represents an important step in the continued development of Rezon Bio’s global manufacturing network and reflects the company’s focus on building robust, compliant, and reliable capabilities to support biologic therapies for patients worldwide. The FDA approval of the Warsaw-Duchnice facility follows a comprehensive review process and reflects the maturity of the site’s quality systems, technical capabilities, and operational readiness for commercial supply to the US market. This approval is coming subsequent to previous EMA GMP certification and approval for commercial supply to European markets. Such approval further strengthens Rezon Bio’s ability to support clients in needs to supply EU and US territories and enhances its position as a reliable partner within the Contract Development and Manufa

Vasion® Achieves FedRAMP® High Authorization, Meeting Federal Cloud Security Gold Standard18.2.2026 14:00:00 CET | Press release

FedRAMP Authorization validates Vasion’s secure, cloud-native, intelligent physical and digital print automation platform as trusted to modernize federal agency operations. Vasion, a leader in serverless printing and Intelligent Print Automation, today announced it has achieved FedRAMP® High Authorization to Operate (ATO) through the Federal Risk and Authorization Management Program. This authorization represents the most rigorous security compliance standard for the government sector. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260218295773/en/ At V3, Vasion Co-Founder and CEO Ryan Wedig unveiled the Intelligent Print Automation platform and challenged every Vasioneer to embrace a Mission of Aspirational Performance that demands collaboration, creativity, and courage. With Vasion's recent FedRAMP High Authorization, the company is making digital transformation attainable for everyone, including federal agencies with the

In our pressroom you can read all our latest releases, find our press contacts, images, documents and other relevant information about us.

Visit our pressroom
World GlobeA line styled icon from Orion Icon Library.HiddenA line styled icon from Orion Icon Library.Eye