
Insulin Developer and Manufacturer
March 22, 2024DayNovo Nordisk registered the phase II clinical trial of NN0519-0130 for weight loss and blood sugar reduction on the Clinicaltrials.gov website, planning to enroll 343 and 288 patients respectively, with an expected preliminary completion in November 2024.


Both Phase II clinical trials used Tirzepatide as the positive control group.

According to the planned timeline of Novo Nordisk's R&D pipeline, NN0159-0130 is most likely a once-weekly injectable GLP-1R/GIPR dual agonist.

The phase I clinical data of the GLP-1R/GIPR dual-target agonist are as follows: The hypoglycemic dosing regimen is 3mg administered for three weeks, once a week, followed by 6mg administered for one week. The weight loss dosing regimen consists of five escalating doses administered daily, starting from 0.3mg and escalating to 3mg over a total of 15 weeks. After four weeks of hypoglycemic treatment, HbA1c decreased by more than 0.5%, and after 15 weeks of weight loss treatment, body weight decreased by nearly 12%.

Based on the phase I clinical registration information of NNC0519-0130 and the phase II clinical control group being Tirzepatide, it can be basically confirmed that this project is a GLP-1R/GIPR dual-target agonist.

AboutNovo Nordisk

Novo Nordisk, founded in 1923, is a global leading biopharmaceutical company headquartered in Copenhagen, the capital of Denmark. Our goal is to drive change to defeat diabetes and other serious chronic diseases such as obesity, rare blood disorders, and endocrine disorders. To achieve this, we lead scientific breakthroughs, expand the accessibility of our medicines, and are committed to preventing and ultimately curing these diseases. Novo Nordisk has approximately 47,000 employees across 80 countries and regions worldwide and provides products and services to more than 168 countries and regions globally.