Download a fully functional 30-day trial version of either StatXact® - the most widely used exact statistics software or LogXact® for small-sample logistic regression.
Cytel's validated clinical trial software and services are proven to help better plan and implement trials that not only meet the study objectives, but also improve the sponsor's overall clinical development strategy.
Whether adaptive or traditional, frequentist or Bayesian, phased or seamless, sponsor companies worldwide rely on Cytel's statistical expertise and clinical know-how to determine and execute approaches with the best chance of success.
By reducing the number of patients and amount of time typically needed to conduct a clinical study, adaptive trials are today helping increase pipeline efficiency. They provide an essential edge in moving your products through the clinical development process.
Pioneers of the statistics behind adaptive designs, Cytel's experience in interim analysis studies, trial simulations, clinical data and supply forecasting is relied upon by the world's top biopharmaceutical companies and research institutions.
In the 2-Feb afternoon workshop, Cytel biostatistical experts explore emerging best practices for determining the optimal adaptive design and study execution strategies.
Adaptive trial experts from Cytel review recent biologic studies utilizing adaptive methods, including innovative oncology treatment studies.
Cytel's VP of Adaptive Trials, Judith Quinlan speaks on advancements in approaches and tools to better manage interim clinical data handling and efficient implementation of committee's decisions.
Acclaimed statistical pioneer C. R. Rao honored by biostatisticians Cyrus Mehta, Martin Posch and Frank Bretz among other conference speakers.
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Nitin Patel and Judith Quinlan to present more efficient approaches and new tools for systematic execution of adaptive clinical trials
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CTO and Co-Founder Dr. Nitin Patel reveals key role of simulation in planning design and implementation of adaptive clinical trials
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