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Our innovative preclinical solutions empower your drug development journey with cutting-edge analytics and insights from inception to preclinical stages.

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We help you navigate complex trial phases efficiently with data-driven methods & strategies tailored to Phase I-III trials for accelerated drug development.

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Maximize your market potential and optimize your commercial strategies with our advanced analytical methods, data science, and tailored commercialization solutions for data-driven commercial success.

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Real-World Evidence Solutions

Harness the power of real-world data and real-world evidence to gather insights and shape future drug development cycles for enhanced efficacy and regulatory compliance.

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Craft optimal trial designs with our advanced analytical methods to enhance efficiency and increase the probability of success throughout your drug’s lifecycle.

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Empower your trial delivery by transforming trial designs into actionable strategies with our data-driven approach to ensure seamless delivery and successful outcomes.

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Unlock the power of data with our methods for actionable insights to drive informed decisions and optimize clinical trial outcomes.

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We offer tailored analytics solutions for your specialized or niche projects enabling you to optimize both efficiency and precision in drug development.

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Enhance your clinical trial design with our strategic consulting services, featuring adaptive trial models and comprehensive regulatory guidance to ensure innovative, compliant, and successful trial outcomes.

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Experience the future of flexible strategic partnerships with Analytics on Demand, providing adaptive and innovative solutions that transcend traditional models to achieve unparalleled operational excellence.

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Project-Based Analytical Solutions

Maximize efficiency and outcomes with our project-based services, delivering specialized expertise, end-to-end biometrics, and focused solutions for unique projects, ensuring timely completion and exceptional results.

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Trial Design Software

Cytel's software platform enables precise trial design and simulation, utilizing adaptive and Bayesian tools to optimize protocols and accelerate drug development with confidence and efficiency.

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Trial Implementation and Decision Support Software

Our unique software package streamlines trial implementation with intuitive solutions for protocol development, randomization, and patient management, optimizing operational efficiency and ensuring study success.

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Split-Dose Cisplatin Use, Eligibility Criteria, and Drivers for Treatment Choice in Patients with Locally Advanced or Metastatic Urothelial Carcinoma: Results of a Large International Physician Survey. O’Dwyer R, Junker S, Szulkin R, Kienzle S, Kearney M, Sridhar SS. Cancers (Basel). 2025

Assessing the economic impact and healthcare resource utilization of inpatient pneumococcal disease among adults: a French national claims database study. Bailey MD, Farge G, Breau Brunel M, Mohanty S, Roy G, de Pouvourville G, de Wazieres B, Janssen C, Tauty S, Bugnard F, Goguillot M, Bénard S, Johnson KD. J Med Econ. 2025

Real-world experience with filgotinib for rheumatoid arthritis in Germany : A retrospective chart review. Schultz O, Fiehn C, Kneitz C, Picker N, Kromer D, Zignani M, De Leonardis F, Orzechowski HD, Gurrath M, Krüger K. Z Rheumatol. 2025

Treatment persistence and clinical outcomes in patients starting B cell depleting therapies within the Swiss MS Cohort. Disanto G, Schaedelin S, Oechtering J, Lorscheider J, Galbusera R, Finkener S, Achtnichts L, Lalive P, Müller S, Pot C, Hoepner R, Salmen A, Zecca C, Hemkens LG, D’Souza M, Fischer-Barnicol B, Du Pasquier R, Roth P, Yaldizli Ö, Einsiedler M, Derfuss T, Kappos L, Gobbi C, Granziera C, Uginet M, Maceski AM, O’Neill K, Leppert D, Benkert P, Kuhle J; Swiss MS Cohort Study. Mult Scler J Exp Transl Clin. 2025

Influence of Treatment Effect Modifiers in Fabry Disease: A Systematic Literature Review. Azimpour K, Tordoff-Gibson C, Dorling P, Koulinska I, Kunduri S, Laliman-Khara V, Forsythe A. Adv Ther. 2025

Developing a prototype for federated analysis to enhance privacy and enable trustworthy access to COVID-19 research data. Eradat Oskoui S, Retford M, Forde E, Barnes R, J Hunter K, Wozencraft A, Thompson S, Orton C, Ford D, Heys S, Kennedy J, McNerney C, Peng J, Ghanbariadolat H, Rees S, H Mulholland R, Sheikh A, Burgner D, Brockway M, B Azad M, Rodriguez N, Zoega H, J Stock S, Calvert C, E Miller J, Fiorentino N, Racine A, Haggstrom J, Postlethwaite N. Int J Med Inform. 2025

Delayed Transition to 20-Valent Pneumococcal Conjugate Vaccine in Pediatric National Immunization Programs: Forgone Public Health and Economic Benefit. Perdrizet J, Ta A, Huang L, Wannaadisai W, Ilic A, Hayford K, Sabra A. Infect Dis Ther. 2025

Economic Evaluation of Transitioning to the 20-Valent Pneumococcal Conjugate Vaccine in the Dutch Paediatric National Immunisation Programme. Çakar E, Ta A, Peters M, Vinand E, Waterval-Overbeek A, Ilic A, Perdrizet J. Infect Dis Ther. 2025

Conus medullaris termination: Assessing safety of spinal anesthesia in the L2-L3 interspace. Paul JE, Udovic LA, Oman K, Kim T, Bernstein L, Matteliano L, Singh N, Caldwell A, Vanniyasingam T, Thabane L. Acta Anaesthesiol Scand. 2025

Real-world therapy and persistence of patients with neovascular age-related macular degeneration and diabetic retinopathy or diabetic macular edema: a German claims data analysis. Krieger J, Cox O, Flacke JP, Beilschmidt L, Mueller S, Maywald U, Koss MJ. Graefes Arch Clin Exp Ophthalmol. 2025

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