Cytel

Company founders Cyrus Mehta, Ph.D. and Nitin Patel, Ph.D. are amongst the pioneering statisticians credited for developing the underlying statistical methods behind so-called “flexible” designs: group sequential and adaptive trials.[5]

Cytel statisticians have collectively published over 140 papers in peer-reviewed statistical and medical journals.[6]

Cytel's Consulting arm focuses on optimizing the approach for biopharma clinical research development objectives. Functional elements their Strategic Consulting team claims to provide include:

• Adaptive Trial Design and Implementation
• Collaborative Research Projects
• Program and Portfolio Optimization
• Regulatory Interactions
• Multiplicity
• Missing Data
• DMC Membership
• Independent Statistical Committee
• Advanced real-world analytics
• Health Economics and Outcomes Research

Cytel's Clinical Research Services arm focuses on improving the probability of success for biopharma clinical research development efforts. Functional elements their Clinical Research Services team claim to provide include:

• Support for DMCs
• Randomization Services
• Clinical Data Management
• Biostatistics
• Statistical Programming
• Medical Writing
• CDISC Migration
• Regulatory Submissions
• Quantitative Pharmacology
• Pharmacometrics
• Data Science
• Complex and Innovative Designs

East East Clinical trial statistical software for the design, simulation and monitoring of adaptive, group sequential and fixed sample size trials. As of 2019, East 6.5 is in use at over 140 pharmaceutical and biotechnology companies, research centers and regulatory agencies including the FDA's Center for Drug Evaluation and Research, Center for Biologics Evaluation and Research and Center for Devices and Radiological Health divisions.[7]

First introduced by the Cytel Software Corporation in 1995 as “East DOS”, the name is derived from the benefit of “Early stopping” a trial due to futility: a failure of the tested treatment to demonstrate significant improvement over an existing treatment and/or placebo.[8]

Enforesys Introduced by Cytel in 2015, Enforesys is a feasibility study decision-making tool for predicting recruitment milestones. Enforsys utilizes historical study site-level data and simulation models to calculate a numerical probability of success for study enrollment strategies.

Compass Compass is used by biostatisticians and clinicians to plan and design earlier stage adaptive clinical trials (traditionally known as phase 1 human tolerance and phase 2 dose-selection studies).

Compass is the first commercially offered adaptive trial composition software with both frequentist and Bayesian methods. Other key capabilities include R code integration, trial simulation compute engines, plus various tables, charts and graphs to visualize and communicate trial design attributes.

StatXact Statistical software based on the exact branch of statistics used for small-sample categorical and nonparametric data problem-solving. Utilized by statisticians and researchers in all fields of study, the StatXact software now has 150 different non-parametric statistical tests and procedures.

Initially offered in 1989 as StatXact DOS, StatXact 8 was released in 2007. The StatXact PROCs variant integrates with the popular SAS statistical software.

LogXact A logistic regression predictive modeling software package suited particularly to cases involving small samples and / or missing data. Logistic regression is used extensively in the medical and social sciences as well as marketing applications to predict subject behavior.

First made available in 1996 under the name LogXact Turbo, LogXact was introduced in 2007 and is currently in its eleventh release. The LogXact PROCs variant integrates with the popular SAS statistical software.

ACES Cytel's web-based Access Controlled Execution System. ACES simplifies compliance with the related FDA guidance and EMA guidelines by a secure means of communicating a clinical trial's interim analysis results and recommendations between the Data Monitoring Committee (DMC/DSMB), Independent Statistical Center and clinical team members. The validated system automatically creates an audit trial, allowing regulators to readily determine "who saw what and when".

SiZ In 2012, SiZ as a stand-alone product was deprecated, and its feature set was consolidated into the company's East product.

OK GO OK GO is the first commercially available software to support the implementation of a quantitative go/no-go decision-making framework in clinical trials.

United States

• Cambridge, Massachusetts (HQ)
• Waltham, MA
• King of Prussia, PA
• San Jose, CA

Canada

• Toronto, ON
• Vancouver, BC

Europe

• Geneva, CH
• Paris, FR
• Barcelona, ES
• Basel, CH
• London, UK
• Rotterdam, NL

Asia

• Shanghai, CN
• Singapore, SG

India

• Pune
• Hyderabad[9]
• Bengaluru
• Mumbai
• Ahmedabad

• Biostatistics
• Clinical research
• Drug development
• Journal of the American Statistical Association
• Randomization
• Sample size determination