4 results match your criteria: "C-ENDO Diabetes and Endocrinology Clinic Calgary[Affiliation]"

Article Synopsis
  • Cagrilintide and semaglutide, used together (CagriSema), are being tested for weight loss in adults with type 2 diabetes, in a study where over 1,200 participants were randomly assigned to receive either the drug combination or a placebo.
  • After 68 weeks, the group receiving CagriSema experienced an average weight loss of 13.7%, significantly higher than the 3.4% weight loss in the placebo group, with many patients achieving at least 5% weight reduction.
  • Additionally, more individuals in the CagriSema group reached healthier blood sugar levels, while gastrointestinal side effects were more common among those taking the drugs compared
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Introduction: The evoke/evoke+ trials are investigating semaglutide in a population with early Alzheimer's disease (AD). Specific analyses of semaglutide safety data in older adults are limited; therefore, in the current analysis, we aimed to evaluate safety considerations with semaglutide in adults ≥ 65 years.

Methods: Adverse event (AE) data from three semaglutide phase 3a programs in participants ≥ 65 years with type 2 diabetes and/or overweight/obesity were pooled.

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Aims: This analysis evaluated whether gastrointestinal (GI) adverse events (AEs) including nausea, vomiting, diarrhoea (N/V/D) and dyspepsia were associated with weight reduction with tirzepatide across the SURMOUNT-1 to -4 trials.

Materials And Methods: SURMOUNT-1 to -4 were global Phase 3 clinical trials evaluating the safety and efficacy of tirzepatide among participants with obesity or overweight with or without type 2 diabetes (T2D). Participants were randomly assigned to receive once weekly subcutaneous tirzepatide or placebo.

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Background: This trial assessed the efficacy and safety of the GLP-1 analogue once a week subcutaneous semaglutide 2·4 mg versus semaglutide 1·0 mg (the dose approved for diabetes treatment) and placebo for weight management in adults with overweight or obesity, and type 2 diabetes.

Methods: This double-blind, double-dummy, phase 3, superiority study enrolled adults with a body-mass index of at least 27 kg/m and glycated haemoglobin 7-10% (53-86 mmol/mol) who had been diagnosed with type 2 diabetes at least 180 days before screening. Patients were recruited from 149 outpatient clinics in 12 countries across Europe, North America, South America, the Middle East, South Africa, and Asia.

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