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Orforglipron
Orforglipron is currently being researched as a once daily oral glucagon like peptide-1 (GLP-1) receptor agonist
Unlike injectable GLP-1s Orforglipron is a non-peptide small molecule, making simpler to administer without the need for injections or refrigeration
It can be taken at any time of day, with or without food or water restrictions, and has a half-life of 29 to 49 hours
Orforglipron mimics the effects of the GLP-1 hormone by binding to GLP-1 receptors in the body. This stimulates insulin release from the pancreas in response to meals, inhibits glucagon secretion (which raises blood sugar), slows gastric emptying to promote feelings of fullness, and reduces appetite
As a partial agonist, it primarily affects cyclic AMP signaling, which may lead to less receptor desensitization compared to full agonists
It’s primarily being researched for managing type 2 diabetes (by improving glycemic control) and chronic weight management in adults with obesity or overweight with at least one weight-related condition, such as hypertension or obstructive sleep apnea
Research application
Copied from the handbook as research notes. and not instructions.
- Weeks: 1-2: 3mg once daily
- Weeks: 3-4: 6mg once daily
- Weeks: 5-8: 12mg once daily
- Weeks: 9-12: 18mg once daily
- Weeks: 13-16: 24mg once daily
Week 17+: 36 mgonce daily
- Type 2 Diabetes: Researched tested include 3 mg, 12mg, and 36mg daily for 40 weeks
Weight Management: Researched tested 12mg, 24mg, or 36mg daily were studied, with higher doses achieving up to 12% body weight reduction over 72 weeks in adults with obesity or overweight with comorbidities
Unless other wise noted intermuscular (IM) peptides are commonly administered via subcutaneous (SQ) injection with 30-31 gauge syringes
From @BowTiedYukon