Novotech Releases 2024 Report on Pancreatic Cancer Clinical Trials and Drug Development
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, Pancreatic Cancer- Global Clinical Trial Landscape (2024).
This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20240903868547/en/
The landscape of pancreatic cancer (PC) research is experiencing a transformative phase, with significant advancements in clinical trials, drug development, and therapeutic strategies. The 2024 Global Clinical Trial Report offers critical insights into these developments, showcasing the growing global effort to combat one of the most lethal forms of cancer.
Key Highlights:
Global Clinical Trials:
- Over 2,000 PC clinical trials have been initiated worldwide since 2019, with North America and the Asia-Pacific region leading the charge, each contributing 38% and 37% of the trials, respectively. Europe follows with a 20% share.
- The United States leads North America with 88% of the trials, while Mainland China dominates the Asia-Pacific region with 43% of trials. Other key contributors include Australia, South Korea, and Japan.
Drug Development Landscape:
- The report identifies 164 drugs in preclinical stages and 233 in early-phase clinical trials, 29 in Phase III, and 11 already on the market, highlighting a robust and growing pipeline aimed at improving treatment outcomes for PC patients.
- Notably, small molecules remain the primary focus of development, with prominent companies such as Astellas Pharma Inc., Bristol Myers Squibb Co., and Eli Lilly and Co. leading the market with their innovative treatments.
- The drug development landscape also includes significant contributions from Pfizer Inc., Roche, and Merck & Co. Inc., with a strong emphasis on targeted therapies and immunotherapies.
Therapeutic Innovations:
- Recent years have seen advancements in neoadjuvant chemotherapy, RAS-directed therapies, and immunotherapy, offering new hope to PC patients. Stroma-modifying drugs are also showing promise in clinical trials, potentially revolutionizing treatment approaches.
- The report predicts that the future of PC treatment will see a greater focus on personalized medicine, early detection methods, and targeted biological therapies, which are expected to significantly improve survival rates and quality of life for patients.
Regional Insights and Trial Density:
- Despite its large population, the Asia-Pacific region's clinical trial density is six times lower than that of the US and about half that of Europe, signaling an urgent need for increased research and targeted medical interventions in these regions.
- The Asia-Pacific region's untapped research potential, combined with its vast patient population and unique genetic diversities, presents a prime opportunity for groundbreaking clinical research and the development of tailored therapeutic interventions.
Leading Contributors:
- Companies like Astellas Pharma Inc., Bristol Myers Squibb Co., and Eli Lilly and Co. have made significant contributions to the PC drug market. The presence of advanced trials by giants such as Pfizer Inc., Roche, and Merck & Co. Inc. underscores the collective global effort to address the challenges posed by pancreatic cancer.
Strategic Insights:
- The SWOT analysis of the pancreatic cancer treatment landscape reveals significant strengths in the development of targeted therapies and immunotherapies, bolstered by increased research funding. However, challenges such as late diagnosis, low survival rates, and the lack of early detection biomarkers persist.
- Opportunities lie in personalized medicine and growing research investments, while threats include stringent regulatory hurdles and the prohibitive cost of advanced treatments, potentially limiting patient access.
The report underscores the critical importance of continued investment in PC research and development. With the backing of leading pharmaceutical companies and innovative clinical trials, the future of pancreatic cancer treatment is bright, offering new hope to patients and their families.
For more information and to download the full report free of charge, please visit Novotech's website or contact our media relations team.
About NovotechNovotech-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
View source version on businesswire.com: https://www.businesswire.com/news/home/20240903868547/en/
Contacts
Media
Media
Toyna Chin
mediacontact@novotech-cro.com
USA: +1 415 364 8135
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
Hemato-Oncology Trials: AOP Health Presents New Results at Top Congress ASH7.12.2025 17:00:00 CET | Press release
AOP Health continues to advance its clinical research program in myeloproliferative neoplasms, a special group of rare blood cancers. The company, specialized in rare diseases, presented the results of two scientific investigations at the 67th American Society of Hematology Association (ASH) Annual Meeting 2025 held in Orlando, FL, USA. The results provide new insights in treatment strategies. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20251207587915/en/ Dr. Martin Steinhart, CEO AOP Health; Photo credit: AOP Health/Studio Koekart ROP-ET and BESREMI PASS One of the clinical studies, ROP-ET, examined the use of ropeginterferon alfa-2b in people with essential thrombocythemia (ET), a disease in which the body produces too many platelets. The trial, a prospective, multicenter, single-arm phase III study, investigated the safety and efficacy of ropeginterferon alfa-2b in ET patients unable to receive available cytoreductive th
CoMotion GLOBAL 2025 Launches in Riyadh: Global Mobility Leaders Unite in Saudi Capital to Chart Urban Future7.12.2025 13:00:00 CET | Press release
Summit debuts Mayors in Motion initiative and CoMotion Urban Visionary Distinction as Riyadh showcases its rise as global mobility testbed Riyadh is rapidly becoming one of the world's most ambitious urban mobility laboratories, where next-generation technologies move from blueprint to real-world deployment on city streets at unprecedented scale. CoMotion GLOBAL 2025, the world's most influential gathering of urban mobility leaders, opens today in Riyadh for a three-day summit bringing together innovators from Africa, Asia, Europe, the Americas, and the Middle East. Running December 7-9, the event will explore how electrification, autonomy, AI-enabled transport, and giga-project urbanism are reshaping cities worldwide. The summit will spotlight everything from high-performance EVs and breakthrough autonomous fleets to emerging-market transport solutions and new mobility models, demonstrating how the Kingdom is opening new pathways for global mobility leadership. Strategic Partnerships
Deciphera Announces Oral Presentation of Positive Topline Results from Phase 2a Study of Sapablursen in Polycythemia Vera at the 67th American Society of Hematology (ASH) Annual Meeting6.12.2025 15:30:00 CET | Press release
Results from Phase 2a IMPRSSION study demonstrate sapablursen significantly reduced phlebotomy rate, controlled hematocrit and increased serum hepcidin Sapablursen was generally safe and well tolerated Results support further development of sapablursen in a Phase 3 study Deciphera Pharmaceuticals, a member of Ono Pharmaceutical Co., Ltd. (Headquarters: Osaka, Japan; President and COO: Toichi Takino; “Ono”), today announced the oral presentation of positive results from the Phase 2a IMPRSSION study of sapablursen in patients with polycythemia vera (PV) at the 67th American Society of Hematology (ASH) Annual Meeting, taking place December 6-9, 2025, in Orlando, FL. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20251206361611/en/ The results were presented by Ionis Pharmaceuticals, who discovered and developed sapablursen and conducted the IMPRSSION study. In March 2025, Ionis and Ono entered into a license agreement in which On
Protagonist and Takeda Present Longer-Term Data at ASH 2025 Showing Rusfertide Delivers Durable Response and Hematocrit Control in Polycythemia Vera6.12.2025 15:30:00 CET | Press release
52-Week Results from the Phase 3 VERIFY Study of Rusfertide Demonstrated Sustained Hematocrit Control and Response, Defined by Absence of Phlebotomy Eligibility, with No New Safety SignalsThese Data Build on Positive 32-Week Primary Analysis from VERIFY, Which Met its Primary Efficacy Endpoint and All Four Key Secondary EndpointsPatients Crossing Over from Placebo to Rusfertide at 32 Weeks Achieved a Similar Response Rate to Those Initially Randomized to Rusfertide, with 77.9% Achieving Absence of Phlebotomy Eligibility Between Weeks 40-52Four-Year Results from the Combined REVIVE and Long-Term Extension THRIVE Study Demonstrated a 13-Fold Reduction in Annual Rate of Phlebotomies from Baseline Protagonist Therapeutics, Inc. (“Protagonist”) (NASDAQ:PTGX) and Takeda (TSE:4502/NYSE:TAK) announce that new 52-week results from the pivotal Phase 3 VERIFY study evaluating rusfertide in patients with polycythemia vera (PV) will be presented in an oral presentation at the 67th American Society
Vertex Presents New Data on CASGEVY®, Including First-Ever Data in Children Ages 5-11 Years, at the American Society of Hematology Annual Meeting and Announces Plan for Global Regulatory Submissions6.12.2025 13:01:00 CET | Press release
- Data from pivotal studies of CASGEVY in children ages 5-11 years with severe sickle cell disease or transfusion-dependent beta thalassemia demonstrates the transformative potential of the therapy in younger patients -- Efficacy and safety data in children 5-11 years are consistent with the durable and positive benefit/risk profile established from clinical studies in patients 12 years of age and older -- Vertex expects to initiate global regulatory submissions for CASGEVY in children 5-11 years in 1H 2026 - Vertex Pharmaceuticals Incorporated (Nasdaq: VRTX) today announced data from multiple studies demonstrating the clinical benefits of CASGEVY® (exagamglogene autotemcel) in people ages 5 years and older living with severe sickle cell disease (SCD) or transfusion-dependent beta thalassemia (TDT). The results, including the first presentation of clinical data from pivotal studies in children ages 5-11 years, and longer-term data from the pivotal studies of people with severe SCD and
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