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news.Alpine Immune Sciences and Horizon Therapeutics have signed an exclusive licence and collaboration agreement to develop protein-based therapies to treat autoimmune and inflammatory diseases.
Alpine Immune, Horizon will develop new protein-based therapies for autoimmune and inflammatory diseases. Credit: National Cancer Institute on Unsplash.
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Alpine Immune Sciences and Horizon Therapeutics have signed an exclusive licence and collaboration agreement to develop protein-based therapies to treat autoimmune and inflammatory diseases.
As agreed, Horizon will gain exclusive rights to develop and commercialise up to four preclinical candidates from Alpine’s discovery platform. This will include licencing of a lead candidate and joint development of other novel candidates.
According to an Alpine statement, these candidates include previously undisclosed multi-specific fusion protein-based therapy candidates.
Under the deal, Alpine will receive an upfront payment of $25m along with a $15m equity investment from Horizon.
In addition, the company is eligible to receive up to $381m per programme, or a total of about $1.52bn, in milestone payments as well as tiered royalties on global net sales.
Alpine president and R&D head Stanford Peng said: “With our combined expertise, we hope to accelerate and expand the potential clinical impact of our discovery platform on autoimmune and inflammatory diseases.”
As per the terms of the agreement, Alpine is responsible for advancing candidate molecules to pre-defined preclinical stage. Subsequently, Horizon will take up the development and marketing activities.
Horizon research and development executive vice president Elizabeth HZ Thompson said: “This partnership represents an opportunity to advance our research efforts, moving our mechanistic insights into innovative molecules utilising Alpine’s expertise and proven ability to design multi-specific protein-based immunotherapies.
“This collaboration will expand Horizon’s early pre-clinical pipeline with complementary mechanisms of action to our current clinical stage therapeutics and provide our first pre-clinical, multi-specific development candidate.”
