TYPE 2 DIABETES MARKET SIZE AND SHARE ANALYSIS - GROWTH TRENDS AND FORECASTS (2024-2031)
Type 2 Diabetes Market, By Drug Class (Dipeptidyl Peptidase-4 Inhibitors, Glucagon-like peptide 1 receptor agonists, Biguanides, Sodium-glucose cotransporter 2 (SGLT2) inhibitors, and Others), By Route of Administration (Oral and Parenteral), By End User (Homecare Settings, Hospitals & Clinics, Academic & Research Institutes, and Others), By Distribution Channel (Hospital Pharmacies, Retail Pharmacies, and Online Pharmacies), By Geography (North America, Europe, Asia Pacific, Latin America, Middle East and Africa)
In June 2023, Pfizer Inc., a multinational pharmaceutical company, announced that it will continue to advance one oral late-stage glucagon-like peptide-1 receptor agonist (GLP-1-RA) candidate into clinical development for the potential treatment of adults with obesity and Type 2 diabetes mellitus (T2DM). Moving forward, the company will advance the clinical program for danuglipron (PF-06882961) based on the outcomes of the ongoing Phase 2 trial, while discontinuing the clinical development of lotiglipron (PF-07081532).
In April 2023, Eli Lilly and Company, a pharmaceutical company, announced that tirzepatide (10 mg and 15 mg) resulted in more weight loss than placebo after 72 weeks of treatment in SURMOUNT-2. The study found that tirzepatide outperformed placebo in terms of both co-primary and key secondary objectives. The trial included 938 adult volunteers with obesity or overweight and type 2 diabetes.
In January 2023, Novo Nordisk, a leading global healthcare company, announced that the U.S. Food and Drug Administration (FDA) issued a label update for Rybelsus (semaglutide) tablets 7 mg or 14 mg, allowing use as a first-line treatment option for adults with type 2 diabetes who have not previously taken a diabetes treatment. This update removes a previous use restriction stating that the medicine should not be used as the first line of treatment for people with type 2 diabetes.
In May 2022, Eli Lilly and Company announced that the U.S. FDA has approved Mounjaro (tirzepatide) injection, a once-weekly glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1 =) receptor agonist indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes. Mounjaro, the first and only S. FDA-approved GIP and GLP-1 receptor agonist, is a single molecule that activates the body's receptors for GIP and GLP-1, both natural incretin hormones.