ABL Bio, Sanofi sign $1bn deal for Parkinson’s candidate ABL301

ABL Bio has bagged a global collaboration and licensing deal worth up to $1.06 billion with Sanofi to develop and commercialize its drug candidate ABL301 for the treatment of Parkinson’s disease.

According to the South Korean biotech firm, ABL301 is a pre-clinical stage bispecific antibody, which targets alpha-synuclein and insulin-like growth factor 1 receptor (IGF1R). Apart from Parkinson’s disease, ABL301 is also being developed for other potential indications associated with enhanced blood-brain barrier (BBB) penetration.

Sanofi will gain worldwide exclusive development and commercialization rights to the bispecific antibody, which uses ABL Bio’s Grabody-B platform technology to cross the blood-brain barrier effectively.

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ABL Bio will be responsible for leading the preclinical development and phase 1 clinical trial of ABL301. Thereafter, its French partner will handle the further clinical development, regulatory approval, and commercialization of ABL301 around the world.

ABL Bio, Sanofi sign $1bn deal for Parkinson's disease candidate ABL301
ABL Bio, Sanofi sign $1bn deal for Parkinson’s disease candidate ABL301. Photo courtesy of Annick Vanblaere from Pixabay.

Sang Hoon Lee — CEO of ABL Bio said: “This groundbreaking partnership with SANOFI proves the immense possibilities of ABL’s innovative bispecific antibody technology.

“We will continue to develop our Grabody-B platform and expand its applicability in other neurodegenerative diseases, such as Alzheimer’s, to contribute to improving the lives of patients worldwide.”

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As per the terms of the agreement, ABL Bio will get upfront payments of $75 million from the French pharma company. Additionally, the South Korean firm is eligible to be paid up to $985 million, which is contingent on meeting predefined development, regulatory, and commercialization milestones. The amount includes a $45 million payment in near-term milestones.

Besides, ABL Bio will also stand to get royalties on net sales if the product from the collaboration with Sanofi is commercialized.

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The deal will come into effect after HSR clearance and other customary closing conditions are met.


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