MA-NOVOTECH
27.8.2024 13:06:28 CEST | Business Wire | Press release
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
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
Incyte Announces New Positive 54-Week Late-Breaking Data for Povorcitinib in Hidradenitis Suppurativa at the 2026 American Academy of Dermatology (AAD) Annual Meeting28.3.2026 20:00:00 CET | Press release
Phase 3 data from the STOP-HS program demonstrate povorcitinib’s substantial and durable clinical efficacy through Week 54 in patients with moderate to severe hidradenitis suppurativa (HS). Through Week 54, clinically meaningful and durable responses were observed across all groups in both STOP-HS1 and STOP-HS2, with up to 71.4% of patients achieving HiSCR50. Improvements in clinical responses across high stringent thresholds were observed, with up to 57% of participants achieving HiSCR75 and up to 29% of participants achieving HiSCR100. Povorcitinib treatment led to consistent reductions across key inflammatory lesion types, with full resolution (ANdT=0) achieved in up to 20% of patients. Additionally, clinically meaningful improvements in quality-of-life measures, including skin pain and fatigue, were observed at Week 54. The overall safety profile of povorcitinib through 54 weeks is consistent with previously reported data, and both doses were well tolerated. Incyte (Nasdaq:INCY) to
Takeda’s Zasocitinib Delivered Rapid and Durable Skin Clearance in a Convenient Once-Daily Pill, Affirming Promise to Reshape Psoriasis Care28.3.2026 20:00:00 CET | Press release
About 70% of patients treated with zasocitinib achieved clear or almost clear skin (sPGA 0/1) at week 16 in Phase 3 plaque psoriasis studies A significantly greater PASI 75 response rate versus placebo was observed as early as week 4 Safety profile consistent with Phase 2b studies with no new safety signals identified Takeda(TSE:4502/NYSE:TAK)today announced new data from the two pivotal Phase 3studies of zasocitinib (TAK-279), a next-generation, highly selective oral tyrosine kinase 2 (TYK2) inhibitor, in adults with moderate-to-severe plaque psoriasis (PsO).1 Presented as a late-breaking abstract at the 2026 American Academy of Dermatology (AAD) Annual Meeting, these data show that convenient once-daily oral zasocitinib demonstrated rapid and durable skin clearance with a safety profile consistent with Phase 2b studies.1,2 “Our goal in psoriasis treatment is clear or almost clear skin, and previously this has been achieved primarily with injectable therapies,” said Melinda Gooderham,
AAD 2026: Late-Breaking Nemolizumab Data Demonstrate Clinically Meaningful Benefits for Children Aged 2 to 11 With Moderate-to-Severe Atopic Dermatitis28.3.2026 16:00:00 CET | Press release
Pharmacokinetics, safety and efficacy clinical study data show that nemolizumab achieved clinically meaningful reductions in skin lesions and itch through Week 16, which were sustained up to a year in children aged 2 to 11 with moderate-to-severe atopic dermatitis1 These findings reinforce the previously established safety and efficacy of nemolizumab in adults and adolescents with moderate-to-severe atopic dermatitis, for which it is approved by multiple global regulatory authorities2,3 Up to 25% of children are affected by atopic dermatitis, and currently there are limited approved treatment options for children living with moderate-to-severe atopic dermatitis4,5 Galderma (SIX: GALD) today announced new phase II data showing that nemolizumab was well tolerated and effective in children (aged 2 to 11 years) with moderate-to-severe atopic dermatitis, with a clinically meaningful and sustained reduction in skin lesions and itch for up to a year.1 Results will be presented in a late-break
Angelalign Technology (6699.HK)Releases 2025 Results: Passion for Clinical Excellence Drives Worldwide Growth27.3.2026 20:56:00 CET | Press release
Angelalign Technology Inc. (6699.HK) (“Angel” or the “Company”) released its financial results for fiscal year 2025. During the reporting period, the Company continued to do well in both the global and China markets. Total case volume was 532,400, which increased 48.1%, revenue was USD 370.3 million, which increased 37.8%, and adjusted net profit was USD 43.8 million, which increased 63.0%. The results were driven by Angel’s passion for clinical excellence and its open and inclusive culture that empowers talented people to work together to meet customer needs, the Company said. Fox Hu, CEO of Angel, stated: “The clear aligner industry is complex and multidisciplinary. It requires top-tier technical and operational talent along with seamless collaboration among professionals from diverse geographies. Angel’s open and inclusive culture attracts professionals who share a passion for clinical excellence and a dedication to bringing outstanding products and services to customers. This melti
Axway Positioned as a Leader in the IDC MarketScape: Worldwide API Management 2026 Vendor Assessment27.3.2026 18:46:00 CET | Press release
Axway, a 74Software company (Euronext: 74SW) and global leader in federated API management and enterprise integration, has been named a Leader in the IDC MarketScape: Worldwide API Management 2026 Vendor Assessment.1 Axway Amplify securely connects, orchestrates, and automates data integration. Organizations in financial services, manufacturing, healthcare, and other industries rely on Amplify to modernize integrations and confidently unlock data to deliver superior digital services faster. The report notes: “The platform benefits from Axway’s long-standing experience in B2B integration, secure file transfer, and legacy connectivity, providing differentiated capabilities for organizations that need to expose and control APIs around core systems that are not cloud-native.”1 This multi-pattern expertise in security, integration, and federated governance — built during the early phases of the API-driven digital transformation — becomes especially critical as enterprises seek to govern dat
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
