Driving Success
in GLP-1 RA Clinical Trials
Empowering Patient-Centric Research in Obesity, Diabetes, and Cardiovascular Health
As GLP-1 receptor agonists (GLP-1 RAs) revolutionize the treatment landscape for obesity, diabetes, and related cardiovascular complications, Signant Health leads the way in capturing critical patient-reported outcomes (PROs) data. Our cutting-edge electronic PRO (ePRO) solutions ensure your clinical trials generate high-quality, reliable evidence to support regulatory approvals and demonstrate real-world patient benefits.
Why Choose Signant Health for Your GLP-1 RA Trials?
Unparalleled Experience:
We've supported over 30 obesity clinical trials evaluating GLP-1 RAs, including pivotal studies leading to regulatory approvals, in addition to over 40 trials in both diabetes and cardiovascular disease.
Global Reach:
Our solutions for obesity clinical trials have engaged over 50,000 patients across 35 countries, with studies lasting up to 5 years.
Comprehensive ePRO Portfolio:
We have experience in supporting a wide range of ePRO measures to assess aspects of health important to patients with these diseases including:
Health-related quality of life (HRQoL, e.g., SF-36, Impact of Weight on Quality of Life-Lite (IWQoL-Lite)(EQ-5D-5L), Food craving (e.g., Control of Eating Questionnaire (CoEQ)), Mental health (e.g., Columbia-Suicide Severity Rating Scale (C-SSRS), Patient Health Questionnaire-9 (PHQ-9)) and other measures such as the Patient Global Impression of Severity/Change (PCIS/C).
Patient-Centric Design:
Our user-friendly ePRO app not only provides an easy and quick way to collect patient-reported outcomes data, but it also helps to guide each patient through each stage of the study by providing up-to-date clinic visit schedules, visit reminders, study information including what to expect at each clinic visit, and easy to use TeleVisit functionality for remote follow up consultations.
Tailored Solutions
for GLP-1 RA Research
Whether you're studying weight loss efficacy, glycemic control, cardiovascular outcomes, or quality of life improvements, Signant Health's ePRO solutions deliver:
Ensuring Success Through Technology, Science, Scale, and Service
Successful clinical trials require more than just technology.
Our approach combines four key elements to drive your GLP-1 RA studies to success:
Solution
Our leading eCOA solution provides comprehensive functionality adaptable to any study protocol, ensuring seamless data collection and management.
Science
With a team of 50+ clinicians and COA scientists, we provide the scientific credibility and expertise needed to generate high-quality, reliable evidence that meets regulatory standards.
Scale
Our robust architectural and operational capacity allows us to support large-scale obesity and diabetes clinical trials across the globe, currently hosting over 600 active ePRO trials.
Service
Experienced project teams, mature operational processes, 24/7 patient and site support, hardware logistics, and comprehensive translations and scale license management ensure smooth trial execution from start to finish.
Proven Track Record
Signant Health has supported 28% of novel drug approvals in the US and EU since 2016. Our solutions have played a crucial role in the successful development and approval of multiple GLP-1 RAs, demonstrating our ability to generate the high-quality data needed to drive regulatory success and market differentiation.