2024 - GlucoseReadyTM: A Comprehensive Digital Platform for Capturing Clinical Data of Cardiometabolic Diseases
Date2024-05-07
Deadline2024-05-07
VenueONLINE-VIRTUAL, USA - United States
KeywordsLife Sciences; Clinical Trials; Medical Device
Topics/Call fo Papers
Newer treatment options, including glucagon-like peptide-1 (GLP1) agents, are under investigation for treating cardiometabolic diseases such as diabetes, weight management/obesity and metabolic dysfunction-associated steatohepatitis (MASH)/non-alcoholic steatohepatitis (NASH). Clinical trial managers have to address regulatory challenges of capturing behavior, symptoms (electronic clinical outcome assessment [eCOA] and hypoglycemia), physical signs (weight, actigraphy and glucose levels), as well as the practical problems of ensuring compliance and avoiding patient dropouts.
Recent US Food and Drug Administration (FDA) guidance has underscored these issues by mandating lifestyle standardization for obesity and diabetes and allowing for the characterization of hypoglycemia triggered by continuous glucose monitoring (CGM) in some diabetes trials to be incorporated as a novel endpoint1.
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In this webinar, attendees will gain insights into current recommendations for monitoring cardiometabolic disease in clinical trials, the complexities and configurability required to continuously monitor patients in this diverse therapeutic area and how clinical trial compliance can be optimized with behavioral modification and lifestyle standardization tools.
Register for this webinar today to gain insights about GlucoseReadyTM, a comprehensive digital platform for capturing clinical data related to cardiometabolic diseases.
1 Food and Drug Administration (2023): Diabetes Mellitus: Efficacy Endpoints for Clinical Trials Investigating Antidiabetic Drugs and Biological Products Guidance for Industry, https://www.fda.gov/media/168475/download
Keywords: Clinical Trials, Obesity, Diabetes, Clinical Research, Biomarkers, NASH, Digital Health, NAFLD, Clinical Data, Therapeutic Areas, Metabolic Disease, Weight Loss, GLP-1 Agonist, Other Software, MASH
Recent US Food and Drug Administration (FDA) guidance has underscored these issues by mandating lifestyle standardization for obesity and diabetes and allowing for the characterization of hypoglycemia triggered by continuous glucose monitoring (CGM) in some diabetes trials to be incorporated as a novel endpoint1.
Read more...
In this webinar, attendees will gain insights into current recommendations for monitoring cardiometabolic disease in clinical trials, the complexities and configurability required to continuously monitor patients in this diverse therapeutic area and how clinical trial compliance can be optimized with behavioral modification and lifestyle standardization tools.
Register for this webinar today to gain insights about GlucoseReadyTM, a comprehensive digital platform for capturing clinical data related to cardiometabolic diseases.
1 Food and Drug Administration (2023): Diabetes Mellitus: Efficacy Endpoints for Clinical Trials Investigating Antidiabetic Drugs and Biological Products Guidance for Industry, https://www.fda.gov/media/168475/download
Keywords: Clinical Trials, Obesity, Diabetes, Clinical Research, Biomarkers, NASH, Digital Health, NAFLD, Clinical Data, Therapeutic Areas, Metabolic Disease, Weight Loss, GLP-1 Agonist, Other Software, MASH
Other CFPs
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- Reimagining the Translation from Biologics Discovery to Development
- Are You Ready for EHR eSource in Clinical Trials? Lessons From the Field
- Electronic Health Records to Electronic Data Capture: Enhancing the Data Journey in Oncology Clinical Trials
- The Incretin Impact: A New Era in Metabolic Disease and Obesity Drug Development
Last modified: 2024-04-13 03:27:13