We approached this by identifying omics- features (i.e., expression, mutation, copy number, pathways, metabolites, etc.) that are predictive of NRF2 CRISPR knockout scores from the DepMap
Research Use Only PE-22-28 has not been evaluated by the FDA for safety or efficacy in humans

References The Lancet (2021) Onceweekly cagrilintide for weight management: phase 2 dosefinding trial (Lau et al.) Int J Mol Sci (2024) Amylin, another important neuroendocrine hormone for treatment of diabesity PMC (2022) Mediators of amylin action in metabolic control The Lancet (2021) Cagrilintide phase 2 trial: 10.8% weight loss at 4.5 mg dose over 26 weeks N Engl J Med (2025) REDEFINE 1: Coadministered cagrilintide and semaglutide in adults with overweight or obesity The Lancet (2021) Cagrilintide + semaglutide phase 1b trial: safety, tolerability, pharmacokinetics (Enebo et al.) J Med Chem (2021) Development of cagrilintide: a longacting amylin analogue Brain Res Rev (2005) Pancreatic amylin as a centrally acting satiating hormone PMC (2006) Pancreatic signals controlling food intake: insulin, glucagon, and amylin PMC (2016) Amylinmediated control of glycemia, energy balance, and cognition Research Resources 5-Amino-1MQ (10 mg & 50 mg Vials) Dosage Protocol Quickstart Highlights 5-Amino-1MQ dosage protocols center on this selective, cell-permeable NNMT (Nicotinamide N-methyltransferase) inhibitor studied for its potential to support fat metabolism, preserve lean muscle mass, and elevate intracellular NAD+ levels [1] [2]

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Weight loss: beyond the GLP-1 conversation GLP-1 drugs like Ozempic deliver results but at a cost rarely mentioned: they cause significant muscle and tissue loss alongside fat
It also provides antioxidant protection by neutralizing free radicals produced as a result of oxidative and metabolic stress