Comprehensive Insight Generation for Product Development
Target RWE generates complete, longitudinal datasets with the power of advanced analytics and vigorous causal inference methodologies to uncover deep insights on unmet needs, disease progression, and the efficacy and safety of new treatments in the real world.
Schedule a MeetingA Partner for Your Clinical Programs
With strong expertise in liver disease, gastroenterology, and dermatology, Target RWE’s multi-stakeholder model allows you to develop robust disease protocols to inform study objectives and endpoints. Our registries contain all relevant disease state variables, which when combined with our digital collection of patient and clinician reported outcomes and biosamples provide a framework for decisions on study entry criteria and site selection – reducing unnecessary procedures and costly protocol amendments.
Demonstrate Valuable Insights with
Real-World Evidence
Target RWE’s cross-sectional and longitudinally complete registries encompass diverse patient populations beyond those traditionally captured in Phase 2 and 3 trials, generating more meaningful evidence on product effectiveness and safety in the real world. We provide insights on natural history of disease, treatment patterns, disease progression and other clinical questions. Execute your publication strategy with confidence and speed by joining our unique collaborative academic model, which taps not just into our patient registries but our network of leading clinical investigators.
Comprehensive Treatment Comparisons for Informed Decision Making
Leverage our proven advanced analytics and diverse real-world data to evaluate comparative effectiveness, safety, and cost-effectiveness of new therapies. Target RWE’s patient-centered analyses utilize patient-reported outcome (PRO) and clinician-reported outcome (ClinRO) measures to inform disease burden, empowering you with the insights necessary to improve healthcare utilization.
Real-World Data for Regulatory Compliance & Safety
Target RWE’s fit-for-purpose longitudinal registries, ability to incorporate clinician-reported outcomes, and validated analytics software provide comprehensive solutions to meet FDA and pharmacovigilance risk assessment committee requests for new drug applications. Our research collaboration agreement with the FDA, combined with proven experience in meeting post marketing commitments and managing adjudication committees, enable us to be your trusted partner for regulatory decision-making.
Patient Insights for Strategic Product Positioning
Target RWE's detailed patient journeys identify meaningful data points in disease that can inform your product positioning and marketing plan. Our large datasets, combined with novel analytical and causal inference methodology identify patient phenotypes with high unmet need, predict disease progression, and support identification of patients who will benefit most from your new therapy.
Fit-for-Purpose Registries for Advanced Research
Target RWE collaborates with a renowned network of clinical investigators to enroll large patient cohorts, capturing up to 5 years of retrospective and 15 years of prospective follow-up – creating some of the largest and most comprehensive real-world patient registries in the U.S.
Therapeutic Area-Relevant Curation for Comprehensive Insights
Target RWE's data curation engine processes complex data using therapeutic area-relevant deterministic rules and machine learning models trained by clinical experts.
Our secure proprietary technology and well-trained natural language processing models curate data from clinician notes, patient-reported outcomes, and other sources to build complete and accurate patient journeys.
Explore our Data Curation Engine
Advanced Causal Inference Analytics
Target RWE's team conducts data-agnostic analyses rooted in modern epidemiological methods and cutting-edge statistical principles. Our proprietary causalRisk™ software offers validated analytics and causal inference methodologies that address complications in real-world data, handling informative censoring, time-varying treatments, or time-varying covariates.
Explore causalRisk™
Powerful Visualizations to Bring Research to Life
Tap into causalPHR™, our interactive and collaborative data visualization software, to explore disease progression and stratify by patient subpopulations of interest. causalPHR™ brings your real world analyses to life, making visualizing, stratifying, and filtering analytical results straightforward and intuitive.
Explore causalPHR™New Publications
Epidemiology
Comparing PCSK9 Monoclonal Antibody Treatment Strategies Following Myocardial Infarction Using Negative Control Outcomes: A Target Trial Emulation Study
Nonalcoholic Steatohepatitis (NASH)
EASL 2024- Real-World Use of Glucagon-Like Peptide 1 Receptor Agonists in Patients with MASLD: A Cross-Sectional Analysis from TARGET-NASH
Nonalcoholic Steatohepatitis (NASH)
EASL 2024- A prospective assessment of disease progression impact on patient-reported outcomes in metabolic dysfunction-associated steatotic liver disease
Gastroenterology
Time to Diagnosis Among Patients with Eosinophilic Esophagitis in the United States
Gastroenterology
Factors Predicting Loss of Remission in Crohn’s Disease Patients in Endoscopic Remission in the Real World Results From TARGET-IBD
Oncology
ISPOR 2024- Assessing The Value Of Linking Abstracted Medical Record Data With Administrative Claims Data To Study Patients With High-Risk Non-Muscle Invasive Bladder Cancer In The United States
In the News
Real World TARGET-NASH Analysis Shows High Concordance Between New MASLD Definitions and Prior TARGET-NASH Pragmatic Definitions
GLP-1 Use and NASH-CHECK Patient-Reported Outcomes Studies from Target RWE Presented at EASL 2024
