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 conventional, frequentist or Bayesian, phased or combined, clinical trial sponsors worldwide rely on Cytel's statistical expertise and clinical know-how to determine and execute the approach most likely to succeed.
By optimizing the number of patients and length of time typically required for a clinical study, adaptive trials are increasing study efficiencies and program success rates. This new breed of trials is an essential edge in moving products through the clinical development process.
Pioneers of the statistics behind adaptive designs, Cytel's unmatched experience with interim analysis studies, trial simulations, clinical data management and supply forecasting is used by all 25 of the world's leading biopharmaceutical companies and hundreds of institutions.
Cytel CTO and Co-Founder Nitin Patel and Medidata President Glen de Vries reveal how simulation and modeling techniques can better forecast trial supply requirements. Complete info and free registration link
ACES® - Access Control Execution System - securely rmanages trials with interim analysis. Eric Silva speaks on on-going studies, FDA and EMA regulations.
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Nitin Patel speaks on new tools to predict product revenue based on modeling and simulation results tuned with updates from clincial data
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Kevin Lee speaks on CDISC Data Submission and SAS-related applications, including manipulatingADaM data sets.
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Cytel and Medidata experts reveal on how advancements in modeling anticipates inventory demands more accurately and how trial supply simulation results are used in adaptive randomization.
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