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Leverage Our Deep Experience in Oncology

Complex studies of cancers require a skilled team with expertise in novel clinical development services and adaptive trial designs, including statistical design, deployment, realworld evidence and industry-leading software. At Cytel, we are equipped with the right experience to accelerate your oncology research by integrating early advisory services and biostatistical expertise. Our comprehensive expertise supports all major types of cancer throughout every drug development phase, ensuring your treatments reach patients faster.

Address Oncology's Unmet Needs with Innovative Strategies

Despite the volume of research, oncology remains among the diseases with the highest unmet patient needs. Study failure rates are high, often attributed to the fact that cancer is a disease of multiple pathophysiologies, many of which are not yet fully characterized, the novel nature of the treatments, and the challenges of accessing patients for research.  

We can help you mitigate these challenges to reveal the full potential of your therapy. We leverage our comprehensive, industry-leading toolkit in innovative trial designs and advanced predictive analytics, together with extensive global networks for access to patient data, and our Axio® Data Monitoring Committee services to enhance the efficiency and effectiveness of oncology trials. 

Our expertise with data and evidence is crucial in a field with such wide-ranging manifestations of disease. 

In particular, real-world evidence and its related methodologies are key quantitative strategies for responding to critical needs within therapeutic development for oncology, including: 

  • Overcoming the hurdles of small sample sizes 
  • The demand for heightened patient safety
  • Ensuring that the critically ill receive therapies quickly and efficiently
  • The expectation that after a trial is over and submission is accepted the therapy will be widely accessible through commercial viability 
  • Understanding patient preferences for different types of therapies and/or formulations
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Make Clinical Trial Decisions with Confidence

The path to regulatory approval for your oncology trial requires expert guidance in clinical development, including statistical design, trial deployment, real-world solutions, and regulatory strategies. 

Cytel’s Strategic Consulting team is made up of specialized, multidisciplinary thought leaders dedicated to advancing the science of oncology trial design. With our deep scientific expertise, unparalleled technology, and pioneering methodologies, we enable you to make clinical trial decisions with confidence. 

Our solutions include: 

White Paper

Read our latest White Paper which describes how to overcome challenges in oncology.

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Download our latest content

Webinar – Project Optimus: Dose Escalation and Stratification Designs in Early Oncology Development
Webinar
July 11, 2024
Webinar – Project Optimus: Dose Escalation and Stratification Designs in Early Oncology Development
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Webinar – FDA’s Project FrontRunner: Reshaping Oncology Drug Development
Webinar
September 16, 2025
Webinar – FDA’s Project FrontRunner: Reshaping Oncology Drug Development
Read More
FDA OCE Project Frontrunner: Accelerating First-Line Oncology Drug Development
Blog
August 5, 2025
FDA OCE Project Frontrunner: Accelerating First-Line Oncology Drug Development
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White Paper – DMCs for Oncology Studies
White Paper
August 20, 2025
White Paper – DMCs for Oncology Studies
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Related Insights

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FDA Guidance on Assessing Overall Survival in Oncology Trials: A DMC Perspective
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Finding the Optimal Biological Dose with New PKBOIN-12 Method
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October 2, 2025
External Control Arms: A Powerful Tool for Oncology and Rare Disease Research
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September 16, 2025
Master Protocols in Oncology Trials
Read More

Claim your free 30-minute strategy session

Book a free, no-obligation strategy session with a Cytel expert to get advice on how to improve your drug’s probability of success and plot a clearer route to market.

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