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Real-World Insights

From biomarker discovery and validation to trial design and label expansion, QIAGEN Real-World Insights (RWI) helps you bridge the gap between actionable insight and real-world action.

Advance drug development with data from precision medicine testing

The majority of cancer patients today are diagnosed and treated outside the context of clinical research—that is, in the real world. 

To improve the efficiency, efficacy, and cost of clinical trials, pharmaceutical companies are using real-world data at each stage of the drug development process.

QIAGEN’s RWI portfolio combines robust real-world genomic data from over 200,000 cancer cases and advanced analytics to optimize biomarker selection, maximize trial success, and shorten drug development timelines.

RWI Applications:

“QIAGEN is helping to take cancer drug development to the next level by aligning the real-world data and comprehensive analyses needed to support biomarker and indication selection for trial stratification and CDx labeling with the superior technical design, regulatory expertise, and manufacturing excellence that are required to deliver the precision CDx that will identify the patients who will derive the most benefit from the targeted therapies."

Sheryl Elkin, Ph.D.
Chief Scientific Officer at N-of-One, a QIAGEN company

How is RWI driving impact? 

QIAGEN RWI is a professional and personalized service empowering pharmaceutical companies to better understand their target populations. RWI helps you get drugs to market faster, expand their usage to new indications, and confidently answer critical questions, such as:

  • Which biomarkers to target?
  • What variants to include?
  • Which patients to select?

Real-World Insights Applications

Biomarker and Cancer Indication Selection

Deciding which biomarkers to include and what technology to use is neither simple nor straight forward. Clinical relevance, reliability, and practicality are of critical importance when selecting biomarkers.

Using robust genomic sequencing data and molecular testing trends, QIAGEN RWI analyses can identify, prioritize and validate biomarkers of therapeutic response and resistance to optimize your drug development strategy.

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Cohort Stratification and CDx Design

Designing an effective trial begins with defining the patient cohort and designing a CDx—a lengthy and iterative process that requires extensive research, testing, and refinement.

QIAGEN RWI  provides the ability to rapidly mine real-world data and link genomic information to specific phenotypes to design a trial tailored to the desired patient cohort and optimized for the highest likelihood of success. 

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Molecular Profiling and Response Analyses

Biomarkers in a patient’s tumor are becoming increasingly critical in determining the appropriate treatment. As more patients undergo diagnostic sequencing, vast amounts of genomic data are being collected, enabling a paradigm shift in how drugs are developed and trials designed. 

QIAGEN RWI provides real-world molecular profiling and drug response data from over 160,000 individual cancer cases to help you better understand the genomic characteristics of your target population.

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Trial Accrual and Drug Market Plan

The prevalence of cancer biomarkers detected in the laboratory differs from what is observed at the bedside. Real-world data helps you better understand the actual numbers of patients with a particular cancer type and where and for which biomarkers they are being tested.

Providing information on current molecular testing trends, QIAGEN RWI allows for an expanded view of cancer indications to be evaluated for your drug for maximum reach and success. 

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Custom Drug Development Projects

Create and deliver bespoke drug development projects with a range of flexible options and services tailored to your unique requirements. Our specialized team works with you to develop the informatics tools and evidence resources you need to get consistent, reliable and actionable results through all phases of your study.

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Leverage Real-World Insights

QIAGEN’s RWI portfolio delivers real-world data from over 160,000 cancer cases to enable better decisions faster in early drug and test development.

To access RWI, you can: 

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Do you have novel questions, hypotheses, and hurdles to overcome? Our team of scientists, bioinformaticists, and clinicians can help you strategize, customize, and deliver within your timeline.

Pharmaceutical Development Bioinformatics Services

From research to regulatory submission, we help you connect data to insight for faster drug discovery and optimized trial design

Biomarker and Indication Selection

Choose the best biomarkers and cancer indications for your molecularly targeted therapies

Molecular Profiling and Response Analysis

Expand beyond the one biomarker, one drug paradigm with expert molecular profiling and drug-response analyses