AI technology company launches with Novartis and Sarepta deals
Collaborations focus on gene therapies for serious eye and muscle diseases using Dyno’s CapsidMap artificial intelligence platform to design AAV vectors.
Dyno Therapeutics emerges from stealth with two strategic collaborations with Novartis and Sarepta to develop improved gene therapies with Adeno-Associated Virus (AAV vectors) based on artificial intelligence (AI) technology.
Novartis collaboration
The biotechnology company's deal with Novartis will focus on developing improved AAV vectors for research, development, and commercialization of gene therapies for ocular diseases.The partnership will allow the parties to utilize Dyno’s CapsidMap AI platform along with Novartis expertise in ophthalmology and gene therapy development and global commercialization to deliver innovative gene therapies to patients with serious diseases of the eye.
According to Eric D. Kelsic, CEO and Co‑founder of Dyno Therapeutics, many eye diseases are particularly suitable for gene therapy treatment, and new and improved AAV vectors could open up more opportunities.
Dyno will use AI technology and its suite of machine learning and experimental tools for the design and discovery of novel AAV capsids, the cell-targeting protein shell of viral vectors, with improved functional properties for gene therapy.
Novartis will conduct preclinical, clinical, and commercialization activities for the gene therapy product candidates created with the novel AAV capsids.
Dyno will receive upfront consideration plus committed research funding and license fees. In addition, Dyno will be eligible to receive clinical, regulatory and sales milestone payments, as well as royalties on worldwide net sales of any commercial products developed through the partnership.
In a separate deal, Dyno and Sarepta Therapeutics will work together to develop next-generation AAV vectors for muscle diseases, also using Dyno’s CapsidMap platform.
AI and machine learning technologies have the potential to deliver enhanced vectors for gene therapies. Dyno’s proprietary CapsidMap platform offers new ways to identify novel capsids that could offer improved muscle targeting and immune-evading properties, in addition to advantages in packaging and manufacturing.
Under the terms of this agreement, Dyno will be responsible for the design and discovery of novel AAV capsids with improved functional properties for gene therapy whereas Sarepta will be responsible for conducting preclinical, clinical and commercialization activities for gene therapy product candidates using the novel capsids.
If successful, Dyno could receive more than $40 million in upfront, option and license payments during the research phase of the collaboration.
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.