AbbVie Enters Obesity Drug Race with $2.2B Amylin Deal

AbbVie has made a significant move into the competitive obesity drug market, signing a licensing agreement worth up to $2.2 billion with Danish company Gubra for a long-acting amylin analog. The deal marks AbbVie's late entry into a field dominated by pharmaceutical giants Novo Nordisk and Eli Lilly.
Deal Structure and Financial Terms
Under the terms of the agreement, AbbVie will pay Gubra an upfront sum of $350 million, with the potential for an additional $1.875 billion in development, commercial, and sales milestones. Gubra will also be eligible for tiered royalties on global net sales of the drug candidate, GUB014295.
GUB014295: A New Approach to Weight Loss
GUB014295, also known as GUBamy, is a once-weekly subcutaneous injection designed to act as a long-acting analog of the amylin hormone. Amylin agonists work by eliciting feelings of satiety, suppressing appetite, and slowing gastric emptying, potentially offering an alternative to the popular GLP-1 medications currently dominating the market.
Early clinical data from Gubra's phase 1 trial showed promising results. Healthy lean and overweight male subjects who received a single high dose of GUB014295 lost approximately 3% of their body weight over six weeks, compared to a 1% weight gain in the placebo group. A multiple-ascending dose study is currently underway, with interim results expected in April 2025.
The Competitive Landscape of Obesity Treatments
AbbVie's entry into the obesity drug market comes at a time of intense competition and rapid development in the field. Novo Nordisk and Eli Lilly have established themselves as leaders with their GLP-1 receptor agonists, including semaglutide (Ozempic, Wegovy) and tirzepatide (Mounjaro, Zepbound).
However, the focus is now shifting towards amylin-based therapies. Novo Nordisk is advancing CagriSema, a combination of semaglutide and the amylin drug cagrilintide, although recent Phase III data fell short of expectations. Eli Lilly is also pursuing amylin programs, with its mid-stage candidate eloralintide being tested in combination with tirzepatide.
Other pharmaceutical companies, including Zealand Pharma and AstraZeneca, are also developing their own amylin-based treatments, highlighting the growing interest in this approach to weight management.
References
- Obesity Late-Comer AbbVie Inks Up to $2.2B Amylin Deal With Gubra
AbbVie is joining the amylin arena, though the pharma is still far behind leaders Novo Nordisk and Eli Lilly.
- AbbVie pays Gubra $350M to make late play for obesity space
AbbVie is paying $350 million to join the obesity race. The outlay, plus up to $1.875 billion in milestones, has landed the drugmaker rights to a long-acting amylin analog that is in phase 1 development at Gubra.
Explore Further
What are the specific milestones outlined in the $2.2 billion AbbVie and Gubra deal?
What is the current efficacy and safety data from the phase 1 trial of GUB014295?
How does GUB014295 compare to existing GLP-1 receptor agonists in the market?
What are the distinguishing features of AbbVie's entry into the obesity drug market compared to its competitors?
Are other pharmaceutical companies pursuing similar licensing agreements in the obesity treatment sector?