- |||||||||| Rybelsus (semaglutide oral) / Novo Nordisk
Trial completion, Enrollment change: Prediction of the SEPRA Diabetes Trial in Healthcare Claims Data (clinicaltrials.gov) - Jul 31, 2023 P=N/A, N=2316, Completed, Trial completion date: Dec 2023 --> Aug 2023 | Trial primary completion date: Nov 2023 --> Jun 2023 Active, not recruiting --> Completed | N=1356 --> 2316
- |||||||||| PN127. Breaking News: GLP-1 agonists, SGLT2 inhibitors, CNS Stimulants - Perioperative Implications (South: 205/206) - Jul 20, 2023 - Abstract #ASA2023ASA_664;
Examples of GLP-1 RAs include exenatide (twice-daily and extended-release once-weekly), lixisenatide (once-daily), liraglutide (once-daily), dulaglutide (once-weekly), semaglutide (once-weekly), and oral semaglutide (once-daily)...During this panel, our experts will dissect the multifaceted impact of these medications on anesthetic care and patient safety, offering a comprehensive overview of their perioperative implications. Join us as we navigate the forefront of medical innovation and its intricate connection to the world of anesthesia.
- |||||||||| Rybelsus (semaglutide oral) / Novo Nordisk, Trulicity (dulaglutide) / Eli Lilly
Journal: Efficacy of treatment with glucagon-like peptide receptor agonists-1 in Asian patients with type 2 diabetes mellitus (Pubmed Central) - Jul 18, 2023 Join us as we navigate the forefront of medical innovation and its intricate connection to the world of anesthesia. The presented review describes benefits in glycemic control as well as in the reduction of relative cardiovascular event risks with GLP-1RA treatment in the Asian population, which requires further in-depth research and implies optimal management tactics in patients with T2DM.
- |||||||||| Rybelsus (semaglutide oral) / Novo Nordisk, Ozempic (semaglutide SC once-weekly) / Novo Nordisk
Safety profile of semaglutide in people aged 55 years and over: pooled data from the PIONEER, SUSTAIN and STEP phase 3 clinical programmes (In-Person) - Jul 6, 2023 - Abstract #AAIC2023AAIC_3849; P3 In this small cohort of patients, the metrics of short-term glycemic control and the extrapolated HbA1C values were similar for the daily 7 mg dose versus the alternate-day 14 mg dose Safety data for participants ?55 years were pooled for: people with T2D receiving once-daily oral semaglutide 3, 7 or 14 mg versus comparator (active or placebo) for 26?78 weeks in PIONEER 1?5 and 7?10 (PIONEER pool, N=4186); people with T2D receiving once-weekly subcutaneous semaglutide 0.5 or 1 mg versus comparator (active or placebo) for 30?56 weeks in SUSTAIN 1?5 and SUSTAIN Japan (NCT02207374 and NCT02254291; SUSTAIN pool, N=2825); and people with overweight/obesity (with/without T2D) receiving once-weekly subcutaneous semaglutide 2.4 mg versus placebo for 68?104 weeks in STEP 1
- |||||||||| Rybelsus (semaglutide oral) / Novo Nordisk
Review, Journal: A Peptide in a Pill - Oral Semaglutide in the Management of Type 2 Diabetes. (Pubmed Central) - Jun 15, 2023 Several large clinical studies, the bulk of which are cardiovascular outcome trials, show that GLP-1 RA treatment is safe and tolerated for persons with T2DM and impaired renal function and that it may potentially have renoprotective characteristics. This article focuses on the advances of oral GLP1-RA and describes the key milestones and predicted advantages.
- |||||||||| Rybelsus (semaglutide oral) / Novo Nordisk
Oral Glucagon-like Peptide Receptor Agonist-1 as Adjuvant Treatment in HNF1A-MODY (ENDOExpo) - May 11, 2023 - Abstract #ENDO2023ENDO_1538; After initiation of oral semaglutide, her glimepiride was reduced to 2 mg once daily, her HbA1c improved to 5.4%, and she lost 30 lbs over a 6-month timeframe. This is the first report demonstrating the benefits of oral GLP-1 RA treatment in a patient with HNF1A-MODY, and this clinical case provides further support of use GLP-1 RA use as adjuvant treatment to sulfonylurea in patients with HNF1A-MODY.
- |||||||||| Rybelsus (semaglutide oral) / Novo Nordisk
COMPARISON OF SEMAGLUTIDE ORAL VS SUBCUTANEOUS IN CHRONIC KIDNEY DISEASE (CKD) (Focussed Oral Room 4) - May 4, 2023 - Abstract #ERAEDTA2023ERA_EDTA_1984; oral formulation of semaglutide was equally effective in terms of glucose control and body weight in patients with T2DM and CKD even with more patients on the low-medium doses. Gi side effects were similar with both formulations though the lower number of patients on the higher oral dose does not allow further conclusions Subcutaneous vs oral semaglutide in T2DM CKD patients Sbc semaglutide Oral semaglutide p n 50 n 20 Male % 80 75 0.6 Age (y) 68.5 (SD 10.1) 68.8 (SD 7.0) 0.9 eGFR (ml/min/1.73m2) 48.4 (SD 20.8) 50.5 (SD 19.5) 0.8 143.1 [33.5-723.8] 280.7 [79.9-462.6] 0.6 -6.2 [-10.8, 0] -6.2 [-11.5 0] 0.9 UACr (mg/g) HbA1C% reduction BMI% reduction -6.5 [ -9.0, -2.0] -3.8 [ -4.7, 0] 0.07 Weight loss % -6.4 [-8.7, -1.4] -4.1 [-6.0, 0] 0.2 eGFR difference basal-final ((ml/min/1.73m2) 0 [-4 , 4] -1 [-5, 3] 0.5 UACR difference (basal-final) (mg/g) 2.7 [ -96.5 a 120] 2.2 [-133.8 a 239.0] 0.8 SBP difference (basal-final) (mmHg) 0 [-4 a 5] -1.5 [-10 a a 0] 0.5 DBP difference (basal-final) (mmHG) 0 [-5 a 0] 0 [-10 a 0] 0.6
- |||||||||| lotiglipron (PF-07081532) / Pfizer
Enrollment closed: Trial to Learn About the Study Medicine (PF-07081532) and Rybelsus in People With Type 2 Diabetes and Separately PF-07081532 in People With Obesity (clinicaltrials.gov) - May 3, 2023 P2, N=900, Active, not recruiting, Gi side effects were similar with both formulations though the lower number of patients on the higher oral dose does not allow further conclusions Subcutaneous vs oral semaglutide in T2DM CKD patients Sbc semaglutide Oral semaglutide p n 50 n 20 Male % 80 75 0.6 Age (y) 68.5 (SD 10.1) 68.8 (SD 7.0) 0.9 eGFR (ml/min/1.73m2) 48.4 (SD 20.8) 50.5 (SD 19.5) 0.8 143.1 [33.5-723.8] 280.7 [79.9-462.6] 0.6 -6.2 [-10.8, 0] -6.2 [-11.5 0] 0.9 UACr (mg/g) HbA1C% reduction BMI% reduction -6.5 [ -9.0, -2.0] -3.8 [ -4.7, 0] 0.07 Weight loss % -6.4 [-8.7, -1.4] -4.1 [-6.0, 0] 0.2 eGFR difference basal-final ((ml/min/1.73m2) 0 [-4 , 4] -1 [-5, 3] 0.5 UACR difference (basal-final) (mg/g) 2.7 [ -96.5 a 120] 2.2 [-133.8 a 239.0] 0.8 SBP difference (basal-final) (mmHg) 0 [-4 a 5] -1.5 [-10 a a 0] 0.5 DBP difference (basal-final) (mmHG) 0 [-5 a 0] 0 [-10 a 0] 0.6 Recruiting --> Active, not recruiting
- |||||||||| ID110521156 / Ildong
Discovery of ID110521156, a Small Molecule GLP-1 Receptor Agonist, for the Treatment of Type 2 Diabetes and Obesity (Poster Halls B-C; [Board No. 93]) - Apr 29, 2023 - Abstract #ADA2023ADA_3124; ID110521156 demonstrated no liabilities when tested on a battery of safety pharmacology studies, including cardiovascular, respiratory, and neurobehavioral function assessment. No genotoxicity was observed on Ames, in vitro chromosomal aberration, and in vivo micronucleus test.From these nonclinical study results, ID110521156 might be considered as a potent candidate of small molecule selective GLP-1 receptor agonist to treat type 2 diabetes and obesity.
- |||||||||| Rybelsus (semaglutide oral) / Novo Nordisk, Nodexen (exenatide oral) / NOD Pharm
Oral Delivery of a GLP-1 Agonist with High Bioavailability in Dogs and Humans (Poster Halls B-C; [Board No. 89]) - Apr 29, 2023 - Abstract #ADA2023ADA_3119; No genotoxicity was observed on Ames, in vitro chromosomal aberration, and in vivo micronucleus test.From these nonclinical study results, ID110521156 might be considered as a potent candidate of small molecule selective GLP-1 receptor agonist to treat type 2 diabetes and obesity. While most require injections due to poor oral bioavailability, Rybelsus
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