Metacrine collaborates on development of FGF1 variants for glucose lowering and improving insulin sensitivity
Novo Nordisk will have an option to license the FGF1 program upon achievement of certain research milestones.
Metacrine has entered a collaboration with Novo Nordisk to develop Fibroblast Growth Factor 1 (FGF1) variants for glucose lowering and insulin sensitization.
Metacrine began work on FGF1 following a 2014 seminal study published in Nature, which demonstrated the ability of FGF1 to lower glucose and improve insulin sensitivity in preclinical diabetes models. Metacrine has made significant progress with protein engineering work to improve the pharmaceutical properties of FGF1.
"We are very pleased to be working with Novo Nordisk, a clear global leader in diabetes and diabetes-related disease complications," said Ken Song, MD, President and CEO of Metacrine. "Combining the knowledge and experience of Novo Nordisk with Metacrine's capabilities ensures an ideal path forward for the FGF1 program, with the opportunity to develop a first-in-class therapeutic to treat patients who have diabetes and other conditions related to insulin resistance."
Under the terms of the agreement, Metacrine will continue to be responsible for certain research activities to further develop and characterize novel FGF1 variants. Novo Nordisk will have an option to license the FGF1 program upon achievement of certain research milestones. Financial terms were not disclosed.
Related News
-
News Pharmaceutical Supply Chain People Moves
The latest appointments, promotions, and structural changes across the pharmaceutical supply chain.
-
News Merck KGaA to buy US biotech SpringWorks for US$3.9 billion
The German multinational pharmaceutical company Merck KGaA have signed a deal to buy US biotech company SpringWorks Therapeutics at an equity value of US$3.9 billion in a move to add rare cancer therapeutics to their pipelines.
-
News Cassava Sciences halts Alzheimer's drug trial after limited progress
Cassava Sciences have drawn a close to their investigations and development of the drug simufilam, which they intended to be used for the treatment of Alzheimer’s disease.
-
News US FDA adds haemodialysis bloodlines to devices shortage list
On March 14, 2025, the US FDA published an open letter to healthcare providers citing continuing supply disruptions of haemodialysis bloodlines, an essential component of dialysis machines.
-
News Vertex Pharmaceuticals stock jumps as FDA approves non-opioid painkiller
UK-based Vertex Pharmaceuticals saw their stock shares soar as the US FDA signed off on the non-opioid painkiller Journavx, also known as suzetrigine, for patients with moderate to severe acute pain, caused by surgery, accidents, or injuries.
-
News Lessons from CPHI Milan 2024: Sunny Intervals for Pharma Manufacturing?
As the 2024 CPHI conference wrapped up in Milan, we caught up with L.E.K. Consulting – a global strategy consulting firm with deep expertise in pharma manufacturing – to discuss evolving market perspectives and business outlook. -
News US BIOSECURE Act passed by US House of Representatives
The controversial act, which has already impacted several foreign companies operating in the US, was passed by the House of Representatives on September 9, 2024. It is now headed for the US Senate before it can be signed into law by President Joe Biden... -
News Drug prices agreed upon as part of the US Inflation Reduction Act
The Inflation Reduction Act brought into constitution by the Biden administation in 2022, which proposed a drug price negotiation between the government and pharmaceutical companies, has reached it's first agreement.