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A new drug, Riptatritide, is a glucagon, GIP, GLP1 triple agonist being studied for obesity treatment. In a phase two trial, participants with obesity saw substantial weight loss, with the highest dose group achieving an average weight loss of 24% over 48 weeks, exceeding previously studied medications. Participants at all doses experienced weight loss, and at the highest dose, average absolute weight loss was 58 pounds, leading to improvements in blood lipid profiles and liver fat reduction.
In the study, 100% of participants who reached either the 8 or 12 milligram dose achieved at least a 5% weight loss, a remarkable response rate unseen in other obesity treatments. The tolerability of the drug was similar to other medications. Results showed significant improvements in blood lipid profiles, liver fat reduction, and HbA1c levels, indicating potential benefits in reducing the risk of obesity-related complications such as fatty liver disease.
Riptatritide's impact on liver fat reduction and its potent weight loss effects highlight a new frontier in obesity treatment. With a 100% response rate in achieving clinically significant weight loss, the drug shows promise in addressing obesity-related health complications. The drug's ability to surpass standard weight loss thresholds and improve metabolic parameters demonstrates its potential to revolutionize obesity management.
Riptatritide's efficacy in achieving significant weight loss, improving metabolic markers, and reducing liver fat content signifies a transformative breakthrough in obesity treatment. By outpacing conventional weight loss outcomes, the drug offers a new paradigm in tackling obesity and its associated health risks, paving the way for enhanced clinical management and improved patient outcomes.
Kaggersema, a novel dual medication, combines an Amalyn analog and semaglutide, showing promising results for weight control and glucose management. Clinical trials demonstrated significant reductions in hemoglobin A1C levels, with the combined medication leading to a 2.2% reduction. Additionally, weight loss data revealed notable results, with a 15.5% weight loss observed with the combined medication. The potential of this dual therapy in offering substantial clinical effects suggests a promising avenue in the treatment of obesity.
Orophir Glipron, a new non-peptide oral GLP-1 receptor agonist, offers a convenient and effective solution for weight management. The medication's non-peptide nature eliminates the need for absorption enhancers, simplifying administration and usage. In a phase two study comparing it to an existing GLP-1 agonist, Orophir Glipron demonstrated superior weight loss outcomes across various dosages, potentially revolutionizing obesity treatment with its ease of use and significant efficacy.
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