Generate additional evidence to add depth to your product's superior value proposition. 

With the changing healthcare landscape, it is becoming imperative to demonstrate the real-world effectiveness and safety of products after product launch. Leveraging the experience of our prospective research team, we have the ability to design and conduct observational, non-interventional, pragmatic and patient registry studies to collect a variety of endpoints including patient reported outcomes. Our team is able to provide full-service support for prospective studies including:  protocol development, site selection and management, IRB submissions and approvals, development and maintenance of online EDC tools, patient recruitment, statistical analyses and preparation of final study reports. 

Xcenda has the capabilities to recruit patients from a variety of sources including physicians, health care systems employers and patient advocacy groups. Additionally, we actively recruit patients from pharmaceutical Patient Support Programs managed by our sister company Lash. 

Below are examples of Xcenda’s prospective study offerings:

Observational/Non-interventional Studies
Studies that are designed to evaluate the efficacy and safety for interventions that are used in accordance with standard practice in a real-world setting. 

Burden of Illness Studies
Studies that are designed to measure the economic, patient and caregiver burden associated with a particular disease. 

Patient Registries
Studies that are designed to collect uniform data to evaluate specified outcomes for a population defined by a particular disease or treatment.

Pragmatic Studies
Comparative studies that are designed to evaluate the efficacy of interventions in a real-world setting. 

Time and Motion Studies
Studies designed to collect time and resources associated with a specific treatment or patient population.